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July 20, 2017

INTERSTELLAR BLEND “SPICE” POLYPHENOL POWERHOUSE (100 Spices in 1)

INTERSTELLAR “SPICE” POLYPHENOL POWERHOUSE—100 SPICES

April 16, 2018

PEEL BLEND FLAVONOID POWERHOUSE

Name: PEEL BLEND FLAVONOID POWERHOUSE
SKU: 5690
Availability: InStock
Rating: 5.00 (32 reviews)

Rated 5.00 out of 5 based on 32 customer ratings

(32 customer reviews)

$75.00 – $275.00

SKU: N/A Categories: Exclusive Products, Featured, Home Tag: Featured

20:1 Peel

100g $75 (36 1 tsp Servings)
400g $195 (144 1 tsp Servings)

200:1 Peel

100g $275 (Approx 300 1/8 tsp Servings)

INTERSTELLAR PEEL BLEND FLAVONOID POWERHOUSE

Insulin Sensitivity Restorer/ Diabetes Destroyer

200:1 100g = 300 1/8 tsp servings

20:1 100g = 36 1 tsp servings

*200:1 means it takes 200kg to make 1kg

Fix the oxidative stress and you fix the insulin resistance. Diabetes is a byproduct of free radical damage. Flavonoids are the most powerful free radical scavengers on the planet. The vast majority of flavonoids are in the PEELS— the part everyone THROWS AWAY! No wonder diabetes and insulin resistance is rampant! Don’t believe me??? Check your blood sugar now and eat some orange peels for a few days and check again and you will see a HUGE improvement.

Thousands of scientific studies here:

Increased oxidative stress precedes the onset of high-fat diet–induced insulin resistance and obesity

“We demonstrate that the pathways for reactive oxygen species (ROS) production and oxidative stress are coordinately up-regulated in both the liver and adipose tissue of mice fed an HFD before the onset of insulin resistance through discrete mechanism. “

FLAVONOIDS LOWER BLOOD PRESSURE

”Flavonoids from all 5 subgroups have been shown to attenuate a rise in or to reduce blood pressure during several pathological conditions (hypertension, metabolic syndrome, and diabetes mellitus). Flavones, flavonols, flavanones, and flavanols were able to modulate blood pressure by restoring endothelial function, either directly, by affecting nitric oxide levels, or indirectly, through other pathways.”

Oxidative stress shortens telomeres

“Telomeres in most human cells shorten with each round of DNA replication, because they lack the enzyme telomerase. This is not, however, the only determinant of the rate of loss of telomeric DNA. Oxidative damage is repaired less well in telomeric DNA than elsewhere in the chromosome, and oxidative stress accelerates telomere loss, whereas antioxidants decelerate it.”

Depression, anxiety-like behavior and memory impairment are associated with increased oxidative stress

“Co-occurrence of anxiety–depression like behaviors and memory deficits in rats correlates with elevated oxidative stress.”

Oxidative Stress and Anxiety: Relationship and Cellular Pathways

Anxiety is an alarm going off in your brain saying, “Yo!!! Yeah you!!! We got problems!!!”

“High O2 consumption, modest antioxidant defenses and a lipid-rich constitution make the brain highly vulnerable to redox imbalances. Oxidative damage in the brain causes nervous system impairment. Recently, oxidative stress has also been implicated in depression, anxiety disorders and high anxiety levels. The findings which establish a link between oxidative stress and pathological anxiety have inspired a number of other recent studies focusing on the link between oxidative status and normal anxiety and also on a possible causal relationship between cellular oxidative stress and emotional stress. This review examines the recent discoveries made on the link between oxidative status and normal anxiety levels and the putative role of oxidative stress in genesis of anxiety. We discuss the different opinions and questions that exist in the field and review the methodological approaches that are being used to determine a causal relationship between oxidative and emotional stress.”

Oxidative stress, cellular senescence and aging

“Almost a half century ago, the free radical theory of aging proposed that the reactive oxygen species (ROS) is a key component which contributes to the pathophysiology of aging in mammalian cells. Over the years, numerous studies have documented the role of oxidative stress caused by ROS in the aging process of higher organisms. In particular, several age-associated disease models suggest that ROS and oxidative stress modulate the incidence of age-related pathologies, and that it can strongly influence the aging process and possibly lifespan. The exact mechanism of ROS and oxidative stress-induced age-related pathologies is not yet very clear. Damage to biological macromolecules caused by ROS is thought to result in many age-related chronic diseases. At the cellular level, increased ROS leads to cellular senescence among other cellular fates including apoptosis, necrosis and autophagy. ”

Excessive caloric intake acutely causes oxidative stress

“These results suggest that the initial event caused by overnutrition may be oxidative stress, which produces insulin resistance, at least in part, via carbonylation and oxidation-induced inactivation of GLUT4.”

Oxidative stress and metabolic disorders

“Increased body weight and metabolic disorder including insulin resistance, type 2 diabetes and cardiovascular complications together constitute metabolic syndrome. The pathogenesis of metabolic syndrome involves multitude of factors. A number of studies however indicate, with some conformity, that oxidative stress along with chronic inflammatory condition pave the way for the development of metabolic diseases. Oxidative stress, a state of lost balance between the oxidative and anti-oxidative systems of the cells and tissues, results in the over production of oxidative free radicals and reactive oxygen species (ROS). Excessive ROS generated could attack the cellular proteins, lipids and nucleic acids leading to cellular dysfunction including loss of energy metabolism, altered cell signalling and cell cycle control, genetic mutations, altered cellular transport mechanisms and overall decreased biological activity, immune activation and inflammation. In addition, nutritional stress such as that caused by high fat high carbohydrate diet also promotes oxidative stress as evident by increased lipid peroxidation products, protein carbonylation, and decreased antioxidant system and reduced glutathione (GSH) levels. These changes lead to initiation of pathogenic milieu and development of several chronic diseases. Studies suggest that in obese person oxidative stress and chronic inflammation are the important underlying factors that lead to development of pathologies such as carcinogenesis, obesity, diabetes, and cardiovascular diseases through altered cellular and nuclear mechanisms, including impaired DNA damage repair and cell cycle regulation. Here we discuss the aspects of metabolic disorders-induced oxidative stress in major pathological conditions and strategies for their prevention and therapy.”

Acute oxidative stress and the ketogenic diet

“The mechanisms underlying the efficacy of the ketogenic diet (KD) remain unknown. Recently, we showed that the KD increased glutathione (GSH) biosynthesis. Since the NF E2-related factor 2 (Nrf2) transcription factor is a primary responder to cellular stress and can upregulate GSH biosynthesis, we asked whether the KD activates the Nrf2 pathway. Here we report that rats consuming a KD show acute production of H₂O₂ from hippocampal mitochondria, which decreases below control levels by 3 weeks, suggestive of an adaptive response. 4-Hydroxy-2-nonenal (4-HNE), an electrophilic lipid peroxidaytion end product known to activate the Nrf2 detoxification pathway, was also acutely increased by the KD. Nrf2 nuclear accumulation was evident in both the hippocampus and liver, and the Nrf2 target, NAD(P)H:quinone oxidoreductase (NQO1), exhibited increased activity in both the hippocampus and liver after 3 weeks. We also found chronic depletion of liver tissue GSH, while liver mitochondrial antioxidant capacity was preserved. These data suggest that the KD initially produces mild oxidative and electrophilic stress, which may systemically activate the Nrf2 pathway via redox signaling, leading to chronic cellular adaptation, induction of protective proteins, and improvement of the mitochondrial redox state.”

Autophagy as a Molecular Target of Flavonoids Underlying their Protective Effects in Human Disease.

“Autophagy is a cellular pathway with the ability to maintain cell homeostasis through the elimination of damaged or useless cellular components, and its deregulation may initiate or aggravate different human diseases. Flavonoids, a group of plant metabolites, are able to modulate different molecular and cellular processes including autophagy.

Analyzed publications indicated that imbalance between cell death and survival induced by changes in autophagy play an important role in the pathophysiology of a number of human diseases. The use of different flavonoids as autophagy modulators, alone or in combination with other molecules, might be a worthy strategy in the treatment of cancer, neurodegenerative disorders, cardiovascular diseases, hepatic diseases, leishmaniasis, influenza, gastric ulcers produced by Helicobacter pylori infection, diabetes, asthma, age-related macular degeneration or osteoporosis.”

RLIP76

When you turn off RLIP76 in mice they can’t get cancer, diabetes or become obese.

2-Hydroxyflavanone inhibits RLIP76 and can be found naturally in parsley, onion peels, berries, tea, and citrus fruit peels.

RLIP76 inhibition (via FLAVONOIDS IN orange peel) prevents Obesity, Metabolic syndrome and cancer

“Feeding a Western high-fat diet (HFD) to C57BL/6 mice induces obesity, associated with a chronic inflammatory state, lipid transport, and metabolic derangements, and organ system effects that particularly prominent in the kidneys. Here, we report that RLIP76 homozygous knock-out (RLIP76−/−) mice are highly resistant to obesity as well as these other features of metabolic syndrome caused by HFD. The normal increase in pro-inflammatory and fibrotic markers associated with HFD induced obesity in wild-type C57B mice was broadly and nearly completely abrogated in RLIP76−/− mice. This is a particularly striking finding because chemical markers of oxidative stress including lipid hydroperoxides and alkenals were significantly higher in RLIP76−/− mice. Whereas HFD caused marked suppression of AMPK in wild-type C57B mice, RLIP76−/−. The baseline renal function was reduced in mice had baseline activation of AMP-activated protein kinase, which was not further affected by HFDRLIP76−/− mice as compared with wild-type, but was unaffected by HFD, in marked contrast to severe renal impairment and glomerulopathy in the wild-type mice given HFD. Our findings confirm a fundamental role of RLIP76 in regulating the function of obesity-promoting pro-inflammatory cytokines, and provide a novel mechanism for targeted therapy of obesity and metabolic syndrome.”https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3743508/

“When you get rid of this [RLIP76] gene in a mouse, it would appear that the mouse can’t get obese, it can’t get diabetes, it can’t get high cholesterol and it can’t get cancer,” explained Sanjay Awasthi, M.D., professor in the Division of Molecular Diabetes Research at City of Hope hospital.

RLIP76, a Glutathione-Conjugate Transporter, Plays a Major Role in the Pathogenesis of Metabolic Syndrome

Our recently published studies demonstrate that RLIP76−/− mice used for these studies were found to have marked insulin-sensitivity, and blood glucose was 46% lower than in RLIP76+/+animals (p<0.001). RLIP76−/− mice also had lower total serum cholesterol and triglycerides (43% and 40% of control, respectively; p<0.01) [1]. The hypoglycemia in RLIP76−/− mice is particularly remarkable because markers of oxidative-stress are remarkably increased in the tissues of the RLIP76−/− animals [1], [23]–[25]. Thus, in the absence of RLIP76, increases in these lipid-peroxidation products are insufficient by themselves to turn on any signaling pathway that can increase BG or lipids. Increased gluconeogenesis was particularly remarkable given that the activity of key gluconeogenic enzymes, G6Pase, F1,6-BPase, and PEPCK, in liver of RLIP76−/− mice was significantly inhibited.

Enhanced basal pAMPK levels in RLIP76−/− mice was another salient finding which strengthens the postulate that RLIP76 is a highly effective target for developing interventional strategies for MSy. Resveratrol, commonly used anti-oxidant, is known to activate AMPK which could contribute to its protective effects from high fat diet induced insulin-resistance [53], [54]. AMPK protects cells from stresses that cause ATP depletion by switching off ATP-consuming biosynthetic pathways. AMPK is activated by phosphorylation by an upstream protein kinase known as AMPK kinase. Activated AMPK can phosphorylate and regulate in vivo HMG-CoA, which is key regulatory enzyme of sterol synthesis [43], [47]. HMG-CoA limits the rate of cholesterol synthesis in liver tissue. Lipitor, inhibitor of HMG-CoA, exerts anti-inflammatory effects by lowering plasma cholesterol. Activation of AMPK leads to the inhibition of cholesterol synthesis by the phosphorylation of HMG-CoA reductase [43]. Loss of RLIP76 significantly affects the activation of stress and apoptosis pathway proteins [1], [25], [35]. Activation of AMPK leads to the inhibition of cholesterol synthesis by the phosphorylation of HMGCR. AMPK activation would be a good approach to treat T2D. These medications generally function to increase the effectiveness of insulin-mediated postprandial inhibition of hepatic gluconeogenesis. These findings provide a new insight on the mechanisms of action of hypoglycemic and/or hypolipidemic drugs.

RLIP76 knock-out mice survive well and are active. In our extensive and previously published studies, RLIP76 inhibition specifically leads to targeting signaling of importance in diabetes mellitus and other oxidative stress related conditions like cancers where targeting RLIP76 leads to selective cancer cell death without affecting the survival of normal cells and tissues [1],[31]–[33]. Hence, both global and selectively targeted approaches can be reasonably pursued as required while targeting RLIP76. In conclusion, our results suggest that RLIP76 is a key effector controlled by multiple proteins known to regulate the metabolic abnormalities of diabetes and metabolic syndrome, and that in its absence drugs that target these proteins will fail to function. The specific events that regulate the transport-effector/clathrin-endocytosis activity of RLIP76 (i.e. phosphorylation of RLIP76 by JNK, Akt, AMPK) will be explored in the future studies.

2′-Hydroxyflavanone (a flavonoid in orange peel): A novel strategy for targeting breast cancer

Intake of citrus fruits is known to reduce the risk for incidence of breast cancer. Hence, we tested the efficacy of citrus flavonoid 2′-hydroxyflavanone (2HF) in breast cancer. 2HF inhibited survival, clonogenic ability, cell cycle progression and induced apoptosis in breast cancer cells. 2HF also decreased VEGF levels and inhibited migratory capacity of breast cancer cells. Administration of 2HF led to regression of triple-negative MDA-MB-231 tumors in the mice xenograft model. 2HF decreased the levels of RLIP76 both studies and MDA-MB-231 xenograft model of breast cancer. Western blot and histopathological analyses of resected tumors showed a decline in the levels of survival and proliferation markers Ki67, pAkt, survivin, and cell cycle proteins CDK4 and cyclin B1. 2HF treatment led to inhibition of angiogenesis as determined by decreased VEGF levels and angiogenesis marker CD31 . 2HF reversed the pro-/anti-apoptotic ratio of BAX/BCL-2 by decreasing anti-apoptotic protein BCL-2 and increasing pro-apoptotic proteins BAX and BIM . 2HF also decreased the mesenchymal markers vimentin and fibronectin along with causing a parallel increase in pro-differentiation protein E-cadherin. Collectively, the ability of 2HF to decrease RLIP76, VEGF and regulate critical proliferative, apoptotic and differentiation proteins together provides strong rationale to further develop 2HF based interventions for targeting breast cancer.

It takes about 16 oranges to get a good dose of 2HF. Get the INTERSTELLAR PEEL BLEND instead in either 20:1 or 200:1 concentrations which is like eating that many oranges in just a few small scoops!

AWESOME MADE CONVENIENT!

INGREDIENTS:

Annona cherimola Mill.(cherimoya) peel

Primary Polyphenols / Flavonoids

Rutin

Quercetin-3-glucoside

Quercetin-3-O-glucopyranoside

Quercetin-3-O-arabinopyranoside

Source:
https://academic.oup.com/carcin/article/36/6/656/276738
https://pdfs.semanticscholar.org/4817/079a52c3a6548846ad32839fcf76212f3c93.pdf

Antihyperglycemic Activity of Annona cherimola Miller and Rutin on Alloxan-induced Diabetic Rats

“It can be concluded from the data that EEAc is beneficial in controlling the blood glucose level in experimental diabetic rats and according to in vivo studies it acts as α-glucosidase inhibitor. This effect can be attributed in part to the presence of flavonol glycoside, rutin. In addition, results validate the use of A. cherimola in Mexican traditional medicine for the treatment of diabetes. Finally, it is the first bioassay-guided about the chemistry and antidiabetic properties of A. cherimola.”

Apple peel extract (malus domestica)

Primary Polyphenols / Flavonoids

Quercetin

Quercetin 3‐glycosides

Catechin

Epicatechin

Source:
https://academic.oup.com/jxb/article/54/389/1977/534676

HEALTH BENEFITS OF APPLE PHENOLICS FROM POSTHARVEST STAGES FOR POTENTIAL TYPE 2 DIABETES MANAGEMENT USINGIN VITRO MODELS

“An increasing number of studies indicate that regular intake of fruits and vegetables have clear links to reduced risk of chronic diseases like diabetes and cardiovascular disease. The beneficial effects in many cases have been attributed to the phenolic and antioxidant content of the fruits and vegetables. Apples are a major source of fiber and contain good dietary phenolics with antioxidant function. Previous epidemiological studies have indicated that intake of apples reduces the risk of developing type 2 diabetes. Our studies indicate that this reduced risk is potentially because of the modulation of postprandial glucose increase by phenolics present in apples via inhibition ofα‐glucosidase. Phenolic content was evaluated during 3 months of postharvest storage of four varieties of apples and results indicated positive linkage to enhanced postharvest preservation andα‐glucosidase inhibition. These in vitro results along with existing epidemiological studies provide strong biochemical rationale for further animal or human clinical studies.”

Banana peel (Musa Cavendish) extract

Primary Polyphenols / Flavonoids

Anthocyanin

Gallocatechin

β-carotene

α-carotene

Leucocyanidin

Source:
https://search.proquest.com/openview/0636b430724b0607c2d24741a56ca4c1/1?pq-origsite=gscholar&cbl=816390

https://www.sciencedirect.com/science/article/pii/S0378874199000057

In vitro antioxidant, hypoglycemic and oral glucose tolerance test of banana peels

“Banana fruit is claimed to have antidiabetic effects despite its high calorie content, and its peels also contain vital phytoconstituents including gallocatechin. Previously banana pulp has been studied for antihyperglycemic effects, and in the present investigation antihyperglycemic effect of ethanolic extract of inner peels of Musa sapientum (EMS), Musa paradisiaca (EMP), Musa cavendish (EMC) and Musa acuminata (EMA) fruit was evaluated using oral glucose tolerance test in normoglycemic rats. In vitro antioxidant study was conducted using DPPH, H2O2 radical scavenging assay and ferric reducing power assay. Wistar rats were divided into fourteen groups and twelve groups received different doses of aforementioned extracts, while control group received gum acacia solution and remaining group received standard drug, glimepiride. All the rats received glucose load at a dose of 2 g/kg body weight. Groups treated with EMC and EMA showed significant decrease in glucose level (p < 0.01) at 150 min as compared to control group.

In hypoglycemic study, only EMP 500 mg/kg, p.o. treated group revealed a significant decrease (p < 0.05) in glucose level at 120 min, while other groups did not show any sign of hypoglycemia. In glucose tolerance test, animals treated with EMC and EMA depicted dose dependent antihyperglycemic effect at 150 min while EMS and EMP showed significant reduction in plasma glucose at higher doses. In a similar fashion, EMA i.e. M. acuminata demonstrated highest antioxidant activity followed by EMC against DPPH radical. In ferric reducing power and H2O2 scavenging assay, EMA demonstrated maximal antioxidant activity when compared with other extracts.”

Benincasa hispida peel extract

Primary Polyphenols / Flavonoids

Catechin

Gallic acid

3‐ethylbenzothiazoline‐6‐sulfonic acid

DPPH

Linoleic acid

Source:
https://onlinelibrary.wiley.com/doi/abs/10.1111/j.1745-4514.2011.00643.x

The Pharmacological Importance of Benincasa hispida

“Benincasa hispida phytochemical analysis showed that the major constituents of Benincasa hispida fruits are volatile oils , flavonoids, glycosides, sacchrides, proteins, carotenes, vitamins, minerals, ß-sitosterin and uronic acid. The pharmacological studies revealed that the plant exerted many pharmacological activities , including central nervous effects ( anxiolytic , muscle relaxant , antidepressant , in the treatment of Alzheimer’s disease and to minimize opiates withdrawal signs), antioxidant, anti-inflammatory, analgesic, antiasthmatic, diuretic , nephroprotective , antidiabetic , hypolipidemic and antimicrobial effects .”

Bergamot

Primary Polyphenols / Flavonoids

Neohesperidin

Hesperetin

Neoeriocitrin

Eriodictyol

Naringin

Source:
https://sfamjournals.onlinelibrary.wiley.com/doi/full/10.1111/j.1365-2672.2007.03456.x

Bitter Orange peel extract (Citrus aurantium)

Primary Polyphenols / Flavonoids

Hesperidin

Naringenin

Nobiletin

Limonoids

Naringin

Sineesytin

Source:
https://bmccomplementmedtherapies.biomedcentral.com/articles/10.1186/1472-6882-12-31

HYPOGLYCEMIC AND HYPOLIPIDIMIC ACTIVITY OF ALCOHOLIC EXTRACT OF CITRUS AURANTIUM IN NORMAL AND ALLOXAN-INDUCED DIABETIC RATS

“Diabetes mellitus is a chronic disorder caused by partial or complete insulin deficiency, which produces inadequate glucose control and leads to acute and chronic complications. Premature and extensive arteriosclerosis involving renal, peripheral, and cardiovascular vessels remain the major complication of diabetes mellitus. Alteration in the serum lipid profile is known to occur in diabetes and this is likely to increase the risk for coronary heart disease. A reduction in serum lipids, particularly of the LDL and VLDL fraction and triglycerides, should be considered as being beneficial for the long-term prognosis of these patients.13 Lowering of blood glucose and plasma lipid levels through dietary modification and drug therapy seems to be associated with a decrease in the risk of vascular disease. In the present study, treatment with Citrus aurantium ethanolic extract (500 mg/kg b.w.) in normal rats produced significant decrease in blood glucose level.

The hypoglycemic effect may be due to increased secretion of insulin from the b-cells of the pancreas, i.e., pancreatotrophic action.14 The results were comparable with that of tolbutamide, which acts by stimulation of insulin release,15 thus further confirming that the extract lowers the blood glucose by a similar action. Moreover, Citrus aurantium produced significant beneficial effects in the lipid profile in euglycemic rats, reducing triglycerides, total cholesterol, LDL, and VLDL, and increasing HDL, significantly. The ethanolic extract increased secretion of insulin from b-cells of pancreas; this increased secretion of insulin stimulates fatty acid biosynthesis and also the incorporation of fatty acids into triglycerides in the liver and adipose tissue.16 Alloxan, a beta cytotoxin, induces ‘chemical diabetes’ in a wide variety of animal species by damaging the insulin-secreting cells of the pancreas. Literature sources indicate that alloxan rats are hyperglycemic.17 The use of lower doses of alloxan (150 mg/kg b.w./i.p.) produced a partial destruction of pancreatic b-cells even though the animals became permanently diabetic.

Thus, these animals have surviving b-cells and regeneration is possible.18 It is well known that the sulfonylureas (tolbutamide) act by directly stimulating the b-cells of the Islets of Langerhans More Details to release more insulin and these compounds are active in mild alloxan-induced diabetes where as they.17 Since our results show that tolbutamide reduced the blood glucose levels in the diabetic animals, the state of diabetes is not severe. Prolonged administration of an ethanolic extract of Citrus aurantium leads to significant reduction in blood glucose level, which is in agreement with other studies.18,20 The hypoglycemic activity of the drug was due to the regeneration of pancreatic cells that were partially destroyed by alloxan, and potentiation of insulin secretion from surviving b-cells of the islets of Langerhans.21 Diabetic rats were observed to have increased plasma lipids, which are responsible for several cardiovascular disorders.22 The higher lipid levels seen in diabetic rats was due to increased mobilization of free fatty acids from peripheral depots and also due to lipolysis caused by hormones.23,24 The ethanolic extract leads to regeneration of the b-cells of the pancreas and potentiation of insulin secretion from surviving b-cells; the increase in insulin secretion and the consequent decrease in blood glucose level may lead to inhibition of lipid peroxidation and control of lipolytic hormones.

In this context, a number of other plants have also been reported to have antihyperglycemic, antihyperlipidemic, and insulin stimulatory effects.25,26,27 It is well known that LDL plays an important role in arteriosclerosis and that hypercholesterolemia is associated with a defect relating to the lack of LDL receptors. The decrease of cholesterol and LDL levels achieved by administration of ethanolic extract, demonstrates a possible protection against hypercholesterolemia and the harm this condition brings about. Further studies are needed to identify the chemical constituents of the ethanolic extract of Citrus aurantium that may be responsible for the hypoglycemic and hypolipidemic activity.”

Blueberry peel extract

Primary Polyphenols / Flavonoids

Kaempferol 3-O-glucoside

Myricetin 3-O-arabinoside

Quercetin 3-O-acetyl-rhamnoside

Quercetin 3-O-arabinoside

Quercetin 3-O-xyloside

Source:
http://phenol-explorer.eu/contents/food/95

Antioxidant capacity and α-glucosidase inhibitory activity in peel and flesh of blueberry (Vaccinium spp.) cultivars

“This study was designed to evaluate cultivar variations in phenolic content, anthocyanin content, and antioxidant activity of peel and flesh; and to determine their potential inhibitory effects on α-glucosidase in 33 blueberry (Vaccinium species) cultivars, including 29 rabbiteye (Vaccinium ashei Reade) blueberries, two V. ashei hybrid derivatives, and two northern highbush (Vaccinium corymbosum L.). The relation of phenolic, anthocyanin, and antioxidant activity to α-glucosidase inhibition in blueberries also was investigated. It was found that peel tissue possessed higher levels of total anthocyanins (TA), total phenolics (TP), antioxidant capacity, and α-glucosidase inhibitory activity than flesh tissue in all blueberries tested.

The percentage contributions of peel to whole berry on scavenging capacity against peroxyl free radicals (ROO), hydroxyl radicals (OH), hydrogen peroxide (H₂O₂), and singlet oxygen (¹O₂) radicals, were higher than those of flesh, even though the fruit contained much higher amounts of flesh than peel in terms of dry weight. Cultivars with high levels of phenolic compounds, antioxidant capacities, and α-glucosidase inhibitory activities could be selected for use in blueberry breeding programs to develop new lines with improved health benefits.”

Camellia sinensis fruit peel extract

Primary Polyphenols / Flavonoids

Epigallocatechin

Epicatechin

Gallocatechin

Catechin

Dihydroflavonol

Source:
https://www.sciencedirect.com/science/article/abs/pii/S0003986104004497

bioactivities of tea (Camellia sinensis L.) fruit peel extracts: Antioxidant activity and inhibitory potential against α-glucosidase and α-amylase

“Tea fruit peel is the main byproduct during manufacture of tea seed oil. The great increase in tea seed oil production in recent years brings the challenge of finding application for tea fruit peel. The aims of this study were to obtain tea fruit peel extracts enriched with bioactive compounds by several solvent extraction methods and to evaluate their antioxidant activity and inhibitory potential against α-glucosidase and α-amylase in vitro. Flavonoids and phenolics were accumulated in ethyl acetate, butanol, and chloroform fractions, and these fractions possessed much better antioxidant activities, including scavenging effect on 1,1-diphenyl-2-picrylhydrazyl radicals (DPPH) and 2,2′-azino-bis(3-ethylbenzthiazoline-6-sulfonic acid) cation radicals (ABTS⁺), and reducing activity, compared with those of the 75% ethanol extract and water fraction. Moreover, the ethyl acetate, butanol, and chloroform fractions exhibited excellent inhibitory activity against α-glucosidase, much stronger than that of the positive control (acarbose). These fractions also showed mild inhibition on α-amylase activity.

► Tea fruit peel extracts could be used as natural antioxidant agents. ► Some fractions exhibited excellent inhibitory potential against α-glucosidase. ► Tea fruit peel can be developed as a renewable bioresource.”

Chinese Honey Orange peel extract (Citrus reticulata Blanco)

Primary Polyphenols / Flavonoids

Naringin

Hesperidin

Didymin

Tangeretin

Nobiletin

Source:
https://www.mdpi.com/1420-3049/15/8/5378

A COMPARATIVE STUDY OF IN VITRO TOTAL ANTIOXIDANT, IN VIVO ANTIDIABETIC AND ANTIMICROBIAL ACTIVITIES OF ESSENTIAL OILS FROM LEAVES AND RIND OF CITRUS RETICULATA BLANCO cv. MURCOT (HONEY)

“Citrus reticulata Blanco cv. Murcot (honey) is one of the most important fruit tree crops in Pakistan. A detailed study regarding total antioxidant capacity (TAC), radical scavenging, antidiabetic and antimicrobial effects of the essential oils from leaves (CRL) and rind (CRR) of this plant were investigated. Essential oils obtained from steam distillation process were subjected to 2,2’-azinobis(3-ethylbenzothiazoline-6-sulpohonic acid) (ABTS) radical cation decolourization, ferric reducing antioxidant power (FRAP), 2.2’-Diphenyl-1-picrylhydrazil (DPPH) radical decolourization, lipid peroxide inhibition using linoleic acid emulsion, superoxide anion radical scavenging and iron chelation activity assays. A linear correlation was observed between the percent inhibition of ABTS radical cation and the amount of essential oils from leaves (R2 =0.9978) and rind (R2 = 0.985). The percent superoxide anion radical scavenging activity was found to be 15.25 and 48.75 for CRL and CRR, respectively. The reducing power in terms of FRAP values were found to be 1.2 and 0.173 mM FeSO4 for CRL and CRR, respectively.

Both CRL and CRR exhibited good metal chelating activities, 56.10 and 61.82 for CRL and CRR, respectively. Best results regarding antidiabetic activity were shown by essential oils from leaves of Citrus reticulata with low as well as high concentrations. The oils also showed antibacterial and antifungal activities comparable to chloramphanicol. The data obtained from oils demonstrate the powerful antioxidative, radical scavenging, antidiabetic and antimicrobial properties of the plant. The data presented here shows that Citrus reticulata Blanco cv. Murcot (Honey) extracts have great antioxidant and radical scavenging activity and thus may be used as a good source of natural antioxidants. The in vivo efficacy of Citrus reticulata Blanco cv. Murcot (Honey) oils against diabetes mellitus or other degenerative diseases may be partially attributed to radical scavenging and antioxidant activity of the plant. “

Citrus clementina peel extract

Primary Polyphenols / Flavonoids

Narirutin

Hesperidin

Diosmin

Nobiletin

Sinensetin

Source:
https://www.sciencedirect.com/science/article/abs/pii/S0889157508000513
https://www.sciencedirect.com/science/article/pii/S0308814610010812

Citrus × clementina peel extract mediated fabrication of silver nanoparticles with high efficacy against microbial pathogens and rat glial tumor C6 cells

“This study reports the use of orange (Citrus × clementina) peel aqueous extract (OPE) for one-pot green synthesis of silver nanoparticles (AgNPs) with high effectiveness against various microbial pathogens as well as rat glial tumor C6 cells. The effects of various operational parameters on the synthesis of AgNPs were systematically investigated. The morphology, particle size, and properties of synthesized AgNPs were characterized using UV–visible spectroscopy, x-ray diffraction, x-ray photoelectron spectroscopy, field emission scanning electron microscopy, energy-dispersive x-ray spectroscopy, and Fourier transform infrared spectroscopy. High-resolution transmission electron microscopy shows that the nanoparticles are mostly spherical in shape and monodispersed, with an average particle size of 15–20 nm. Notably, the OPE-synthesized AgNPs were stable up to 6 months without change in their properties.

Low doses of OPE-AgNPs inhibited the growth of human pathogens Escherichia coli, Bacillus cereus, andStaphylococcus aureus. The minimum inhibitory concentration and minimum bactericidal concentration of AgNPs against selected pathogenic bacteria were determined. OPE-AgNPs exhibited strong antioxidant activity in terms of ABTS (2,2′-azino-bis (3-ethylbenzothiazoline-6-sulfonic acid)) radical scavenging (IC₅₀ 49.6 μg/mL) and DPPH (1,1-diphenyl-2-picrylhydrazyl) radical scavenging (IC₅₀ 63.4 μg/mL). OPE-AgNPs showed dose-dependent response against rat glial tumor C6 cells (LD₅₀ 60 μg/mL) showing a promising potential as anticancer agents.”

Citrus depressa Hayata (shiikuwasa) peel extract

Primary Polyphenols / Flavonoids

Citromitin

Tangeretin

Nobiletin

Epicatechin

Quercetin

Source:
https://www.jstage.jst.go.jp/article/jnsv/56/1/56_1_60/_article/-char/ja/
https://bmcplantbiol.biomedcentral.com/articles/10.1186/s12870-016-0870-9

Effects of a Citrus depressa Hayata (shiikuwasa) extract on obesity in high-fat diet-induced obese mice

“Citrus depressa Hayata (commonly known as shiikuwasa) is cultivated in the northern areas of Okinawa, Japan, and used as a juice. In this study, we examined the anti-obesity effects and mechanism of action of shiikuwasa peel extract (SE) using high-fat diet (HFD)-induced obese mice. Mice were fed a low-fat diet (LFD), HFD or HFD containing 1% or 1.5% (w/w) SE (HFD + 1 SE and HFD + 1.5 SE, respectively) for 5 weeks. The body weight gain and white adipose tissue weight were significantly decreased in the HFD + 1.5 SE group compared with the HFD group. The plasma triglyceride and leptin levels were also significantly reduced in the HFD + 1.5 SE group compared with the HFD group.

Histological examinations showed that the sizes of the adipocytes were significantly smaller in the HFD + 1.5 SE group than in the HFD group. The HFD + 1.5 SE group also showed significantly lower mRNA levels of lipogenesis-related genes, such as activating protein 2, stearoyl-CoA desaturase 1, acetyl-CoA-carboxylase 1, fatty acid transport protein and diacylglycerol acyltransferase 1, than the HFD group. These results suggest that the anti-obesity effects of SE may be elicited by regulating the expressions of lipogenesis-related genes in white adipose tissue.”

Citrus medica L. cv Diamante peel extract (rutaceae)

Primary Polyphenols / Flavonoids

β-carotene

Limonene

β-pinene

γ-terpinene

Neral

Geranial

Source:
https://hrcak.srce.hr/index.php?show=clanak&id_clanak_jezik=193397

“This study aimed to investigate the antidiabetic, antilipidaemic and antioxidant activities of Citrus medica cv Diamante (Rutaceae) hydroalcoholic (CD) peel extract in Zucker diabetic fatty (ZDF) rats. The ability of CD to protect against oxidative stress was investigated by using different in vitro assays and in vivo by using the reactive oxygen metabolites-derived compounds (d-ROMs) test and the biological antioxidant potential test (BAP). Two different doses of CD extract (300 and 600 mg/kg/die) were administered at ZDF rats for 4 weeks.

CD reduced cholesterol and triglycerides levels. A dose-dependent effect on body weight and serum glucose levels was observed. A decrease of d-ROMs and an increase of BAP were recorded by using the dose of 600 mg/kg. The extract inhibited lipid peroxidation (IC₅₀ value of 0.23 mg/ml). These findings suggest as an efficient phytotherapeutic approach in combating hyperlipidaemic and hyperglycaemic disorders.”

Cucumis sativus peel EXCTRACT

Primary Polyphenols / Flavonoids

Quercetin

Isovitexin

Isoscoparin

Saponarin

Apigenin

Source:
http://www.orientjchem.org/vol28no2/extraction-of-polyphenol-flavonoid-from-emblica-officinalis-citrus-limon-cucumis-sativus-and-evaluation-of-their-antioxidant-activity/
https://www.sciencedirect.com/science/article/abs/pii/S003194220100156X

Protective Role of Three Vegetable Peels in Alloxan Induced Diabetes Mellitus in Male Mice

“In a preliminary study, effects of ethanolic extracts of Cucurbita pepo, Cucumis sativus and Praecitrullus fistulosus peels were studied at 250 and 500 mg kg⁻¹ d⁻¹ for 15 days in the alterations in serum glucose and in hepatic lipid peroxidation (LPO) in male mice. In the pilot experiment, the effective and safe concentration of each peel was administered (p.o.) for 10 consecutive days and then on 11th and 12th days alloxan was administered along with peel extracts.

The treatment was continued up to 15th day. At the end, alterations in serum glucose, insulin, triiodothyronine, thyroxine, total cholesterol, triglyceride, high density lipoprotein, low density lipoprotein, very low density lipoprotein, hepatic lipid peroxidation, superoxide dismutase and catalase were studied. All the three peel extracts nearly reversed most of these changes induced by alloxan suggesting their possible role in ameliorating diabetes mellitus and related changes in serum lipids. Total polyphenols, flavonoids and ascorbic acid contents of the test peels were also estimated, which appear to be associated with the observed antidiabetic and antioxidative potentials.”

Cucurbita pepo FRUIT peel extract

Primary Polyphenols / Flavonoids

Nigericin

Valinomycin

Thiocyanoacetamide

Isorhamnetin

Kaempferol

Source:
https://link.springer.com/article/10.1007/BF00198044
https://link.springer.com/article/10.1007/BF01917844
https://www.researchgate.net/profile/Roshanlal_Yadav/publication/305409797_Effect_of_cooking_methods_and_extraction_solvents_on_the_antioxidant_activity_of_summer_squash_Cucurbita_pepo_vegetable_extracts/links/57ebf56308ae92eb4d263e92.pdf

Hypoglycaemic and hypolipidemic effects of pumpkin (Cucurbita pepo L.) on alloxan-induced diabetic rats

“This study was aimed to evaluate the hypoglycaemic and hypolipidemic effects of different doses of pumpkin (Cucurbita pepo L.) powder in male diabetic rats. A total of 35 rats were randomized into 5 groups of 7 each as follows: Group 1: Normal control; Group 2: Diabetic control; Group 3: Diabetics administered with low doses of pumpkin powder (1 g/kg); Group 4: Diabetics administered with high doses of pumpkin powder (2 g/kg), and Group 5: Diabetics administered with glibenclamide (0.6 mg/kg), as positive control. The rats were made diabetic by alloxan (120 mg/kg body weight (BW)) injection and were treated for 4 weeks on a daily basis. Blood samples were collected following the experiment. Pancreatic specimens were also collected for histological analysis. Glucose, cholesterol, triglycerides, low density lipoprotein (LDL) and C-reactive protein (CRP) were significantly increased, while insulin was decreased in diabetic rats as compared to the normal control group (p < 0.05). Low dose pumpkin significantly decreased glucose, triglycerides, LDL and CRP as compared to diabetic group and high dose pumpkin decreased cholesterol (p < 0.05). Histological analysis also revealed a significant increase in the diameter and number of langerhans islets in treated group with pumpkin, which was consistent with the latter findings. Therefore, pumpkin might be beneficial in diabetic patients.”

Dracaena cochinchinensis resin (dragons blood) Croton lechleri Müll Arg. (syn. C. draconoides Müll. Arg.)

Primary Polyphenols / Flavonoids

6,4′‐dihydroxy‐7‐methoxy‐8‐methylflavane

5,4′‐dihydroxy‐7‐methoxy‐6‐methylflavane

7,4′‐dihydroxy‐5‐ methoxyhomoisoflavane

7‐hydroxy‐4′‐methoxyflavane

4′,7‐dihydroxyflavane

Source:
https://onlinelibrary.wiley.com/doi/abs/10.1002/hlca.200490106

A Systematic Review of the Botanical, Phytochemical and Pharmacological Profile of Dracaena cochinchinensis, a Plant Source of the Ethnomedicine “Dragon’s Blood”

“Dragon’s blood” is the name given to a deep red resin obtained from a variety of plant sources. The resin extracted from stems of Dracaena cochinchinensis is one such source of “dragon’s blood”. It has a reputation for facilitating blood circulation and dispersing blood stasis. In traditional Chinese medicine, this resinous medicine is commonly prescribed to invigorate blood circulation for the treatment of traumatic injuries, blood stasis and pain. Modern pharmacological studies have found that this resinous medicine has anti-bacterial, anti-spasmodic, anti-inflammatory, analgesic, anti-diabetic, and anti-tumor activities, while it is also known to enhance immune function, promote skin repair, stop bleeding and enhance blood circulation.

Various compounds have been isolated from the plant, including loureirin A, loureirin B, loureirin C, cochinchinenin, socotrin-4′-ol, 4′,7-dihydroxyflavan, 4-methylcholest-7-ene-3-ol, ethylparaben, resveratrol, and hydroxyphenol. The present review summarizes current knowledge concerning the botany, phytochemistry, pharmacological effects, toxicology studies and clinical applications of this resinous medicine as derived from D. cochinchinenesis.”

Durian (Durio zibethinus Murr.) peel extract

Primary Polyphenols / Flavonoids

Catechin

Quercetin

EGCG

Hesperidin

Naringin

Source:
https://www.japsonline.com/admin/php/uploads/1848_pdf.pdf

Antidiabetic Activity of Durian (Durio zibethinus Murr.) and Rambutan (Nephelium lappaceum L.) Fruit Peels in Alloxan Diabetic Rats

“Durian contains flavonoids, namely catechin and quercetin [23] as well as polyphenols and tannins [10]. Quercetin had activity Aldos reductase inhibitors that could potentially be used in therapeutic antihyperglycemia [24]. In the rambutan fruit peels contained flavonoids and tannins [12]. Ethanolic extract of rambutan fruit peels contained quercetin, geraniin [13] and epigallocatechin-3-gallate (EGCG) which had antihyperglycemia activity [14] as well as powerful antioxidants [15]. Based on the content of flavonoids catechin, quercetin and EGCG and polyphenols and tannins, a mechanism thought to decrease blood glucose levels in diabetic rats through inhibition of glucose absorption, stimulates the release of insulin and indirect mechanisms through the antioxidant processes. Glucose binds to proteins can be oxidized and produce Reactive Oxygen Species (ROS).

The combination of glycation and oxidation of glucose produces AGEs (advanced glycogen end-products) in which this process was irreversible long-lasting and can caused tissue damage. That glycated proteins and AGEs-modified proteins can lead to oxidative stress which can trigger the diabetic condition [22]. Another mechanism that was thought to have the effect of decreasing blood glucose levels in test animals, with the occurrence geraniin in rambutan fruit peel extract which had the ability to prevent the formation of AGEs [13].

This research has proven that the ethanol extract of durian rind and rambutan fruit peel can lowered blood glucose levels of alloxan-induced rats. However, the mechanism of the antidiabetic activity of the ethanol extract of durian and rambutan fruit peels was not certainly. So the evaluation to determine the mechanism of molecular pharmacology decrease in blood glucose levels that occurs, needs to be done. In addition it is necessary to ensure what the active compounds are most responsible for its pharmacological activity.”

Grapefruit peel extract (Citrus paradisi)

Primary Polyphenols / Flavonoids

Hesperidin

Naringin

Hesperedin

Narigenin

Rutin

Source:
https://www.sciencedirect.com/science/article/pii/S0308814606000185

PHENOLIC EXTRACTS FROM GRAPEFRUIT PEELS (CITRUS PARADISI) INHIBIT KEY ENZYMES LINKED WITH TYPE 2 DIABETES AND HYPERTENSION

“This study sought to characterize the interaction of phenolic extract from grapefruit peels with α‐amylase, α‐glucosidase and angiotensin‐I‐converting enzyme (ACE) activities. The free phenolic of grapefruit peels was extracted with 80% acetone, while the bound phenolic was extracted from the alkaline and acid‐hydrolyzed residue with ethyl acetate; and their interaction with the enzymes were assessed. The phenolic extracts inhibited α‐amylase, α‐glucosidase and ACE enzyme activities; however, free phenolic had significantly higher (P < 0.05) α‐amylase and α‐glucosidase inhibitory activities than bound phenolic, while there was no significant difference (P > 0.05) in their ACE inhibitory activities. Nevertheless, the extracts were strong inhibitor of α‐glucosidase when compared to α‐amylase. The phenolic inhibited sodium nitroprusside‐induced lipid peroxidation in pancreas in a dose‐dependent manner. Therefore, free and bound phenolic extracts from grapefruit peels could be used as nutraceutical for the management of hypertension and type 2 diabetes.

Type 2 diabetes (including its precursor, metabolic syndrome) is one of the top five most significant diseases in the developed world and is rapidly becoming a burden in sub‐Sahara Africa. Natural inhibitors with relatively mild inhibition of α‐amylase but strong inhibitor of α‐glucosidase activity could be an effective therapy for type 2 diabetes with minimal side effects, while the inhibition of angiotenisn‐I‐converting enzyme is a useful approach in the treatment of hypertension in both diabetic and nondiabetic patients, and phenolics have promising potential. Our findings in this study have shown that grapefruit peels that are usually considered to be waste could be a cheap and good source of free soluble and bound phenolics with antidiabetic and antihypertensive potentials.”

Hawthorn (Crataegus Mexicana) peel extract

Primary Polyphenols / Flavonoids

Quercetin 3-O-glucoside

Quercetin 3-O-rhamnoside

Quercetin 3-O-rhamnosyl

Quer-cetin 3-O-rhamnosyl

Rutin

Source:
https://www.researchgate.net/profile/Margarita_Cervantes-Rodriguez/publication/281443679_Antioxidant-mediated_protective_effect_of_hawthorn_Crataegus_mexicana_peel_extract_in_erythrocytes_against_oxidative_damage/links/55e75b1708ae3e1218420b36/Antioxidant-mediated-protective-effect-of-hawthorn-Crataegus-mexicana-peel-extract-in-erythrocytes-against-oxidative-damage.pdf

Antioxidant-mediated protective effect of hawthorn (Crataegus mexicana) peel extract in erythrocytes against oxidative damage

“This study provides the first in vitro evidence for an active role of C. mexicana as antioxidant on erythrocytes. Hawthorn is a fruit with anti-oxidant potential, reduces morphological changes and extends life span of the red blood cells in vitro. Such protection could be due to the inhibition of membrane lipoperoxidation and oxidative damage in cytoskeletal proteins. The conjunction of antioxidants in this extract, and not just specific purified antioxidants, could be helpful to keep normal the rheology properties of the erythrocyte apparently without any pro-oxidative damage.

The antioxidants present in the acetone extract may contribute to protect the erythrocyte cell membrane against lipid peroxidation induced by oxidative stress, thereby participating in diminishing the morphological and many rheology changes that may happen in the pathogenesis of vasoocclusive diseases, such diabetes mellitus, metabolic syndrome, different types of anemia, and the inhibition of cell storage lesion in RBCs.

More studies are required to correctly identify the bioactive compounds of C. mexicana and how it contribute to the erythrocyte protection, and their mechanisms of action in the protection of the RBCs. This study give the scientific biochemical bases to use hawthorn extracts in a clinical setting, to prevent or treat many diseases and conditions associated to oxidative stress.”

Huyou (Citrus changshanensis) fruit peel extract

Primary Polyphenols / Flavonoids

Naringin

Hesperidin

TAC

Neohesperidin

Neoeriocitrin

Source:
https://www.sciencedirect.com/science/article/pii/S0308814607001410
https://www.sciencedirect.com/science/article/pii/S0308814612009764
https://onlinelibrary.wiley.com/doi/abs/10.1111/jfpp.13278

Purification of naringin and neohesperidin from Huyou (Citrus changshanensis) fruit and their effects on glucose consumption in human HepG2 cells

“Huyou (Citrus changshanensis) is rich in naringin and neohesperidin, which are natural flavanone glycosides with a range of biological activities. Among the different fruit parts, i.e. flavedo, albedo, segment membrane (SM), and juice sacs (JS), albedo showed the highest contents of both compounds, with 27.00 and 19.09 mg/g DW for naringin and neohesperidin, respectively. Efficient simultaneous purification of naringin and neohesperidin from Huyou albedo was established by the combination of macroporous D101 resin chromatography and high-speed counter-current chromatography (HSCCC).

Purified naringin and neohesperidin were identified by both HPLC and LC–MS, and their effects on glucose consumption were investigated in HepG2 cells. Cells treated with naringin and neohesperidin showed increased consumption of glucose, and this was associated with increased phosphorylation of AMP-activated protein kinase (AMPK). Therefore, naringin and neohesperidin from Huyou may act as potential hypoglycaemic agents through regulation of glucose metabolism.”

Jujube (Ziziphus Jujuba Mill.) Fruit peel

Primary Polyphenols / Flavonoids

Procyanidin B2

Epicatechin

Quercetin-3-O-rutinoside

Quercetin-3-O-galactoside

Kaempferol-glucosyl-rhamnoside

Source:
https://pubs.acs.org/doi/abs/10.1021/jf200371r

The Jujube (Ziziphus Jujuba Mill.) Fruit: A Review of Current Knowledge of Fruit Composition and Health Benefits

“The nutritional jujube (Ziziphus jujube Mill.) fruit belonging to the Rhamnaceous family grows mostly in Europe, southern and eastern Asia, and Australia, especially the inland region of northern China. Jujube has a long history of usage as a fruit and remedy. The main biologically active components are vitamin C, phenolics, flavonoids, triterpenic acids, and polysaccharides. Recent phytochemical studies of jujube fruits have shed some light on their biological effects, such as the anticancer, anti-inflammatory, antiobesity, immunostimulating, antioxidant, hepatoprotective, and gastrointestinal protective activities and inhibition of foam cell formation in macrophages. A stronger focus on clinical studies and phytochemical definition of jujube fruits will be essential for future research efforts. This review may be useful for predicting other medicinal uses and potential drug or food interactions and may be beneficial for people living where the jujube fruits are prevalent and health care resources are scarce.”

Kumquat (Fortunella margarita ) peel

Primary Polyphenols / Flavonoids

Acacetin 3,6-di-C-glucoside

Vicenin-2

Lucenin-2 4′-methyl ether

Narirutin 4′-O-glucoside

Apigenin 8-C-neohesperidoside

Source:
https://www.sciencedirect.com/science/article/abs/pii/S0963996910004643

Effects of Fortunella margarita Fruit Extract on Metabolic Disorders in High-Fat Diet-Induced Obese C57BL/6 Mice

“Obesity is a nutritional disorder associated with many health problems such as dyslipidemia, type 2 diabetes and cardiovascular diseases. In the present study, we investigated the anti-metabolic disorder effects of kumquat (Fortunella margarita Swingle) fruit extract (FME) on high-fat diet-induced C57BL/6 obese mice.

The kumquat fruit was extracted with ethanol and the main flavonoids of this extract were analyzed by HPLC. For the preventive experiment, female C57BL/6 mice were fed with a normal diet (Chow), high-fat diet (HF), and high-fat diet with 1% (w/w) extract of kumquat (HF+FME) for 8 weeks. For the therapeutic experiment, female C57BL/6 mice were fed with high-fat diet for 3 months to induce obesity. Then the obese mice were divided into two groups randomly, and fed with HF or HF+FME for another 2 weeks. Body weight and daily food intake amounts were recorded. Fasting blood glucose, glucose tolerance test, insulin tolerance test, serum and liver lipid levels were assayed and the white adipose tissues were imaged. The gene expression in mice liver and brown adipose tissues were analyzed with a quantitative PCR assay.

In the preventive treatment, FME controlled the body weight gain and the size of white adipocytes, lowered the fasting blood glucose, serum total cholesterol (TC), serum low density lipoprotein cholesterol (LDL-c) levels as well as liver lipid contents in high-fat diet-fed C57BL/6 mice. In the therapeutic treatment, FME decreased the serum triglyceride (TG), serum TC, serum LDL-c, fasting blood glucose levels and liver lipid contents, improved glucose tolerance and insulin tolerance. Compared with the HF group, FME significantly increased the mRNA expression of PPARα and its target genes.

Our study suggests that FME may be a potential dietary supplement for preventing and ameliorating the obesity and obesity-related metabolic disturbances.”

Lagenaria siceraria peel extract

Primary Polyphenols / Flavonoids

β-sitosterol

Vanillin

quercetin

Rutin

3-tert-butyl-4-hydroxyanisole

Source:
https://akademiai.com/doi/full/10.1556/1326.2017.00247

Lagenaria siceraria peel extract in the regulation of hyperthyroidism, hyperglycemia and lipid peroxidation in mice

” In conclusion, our present findings reveal that the peel extract of Lagenaria siceraria, not only regulates lipid peroxidation, but also appears to be a promising agent for the amelioration of hyperthyroidism or hyperglycemia.”

Lansium domesticum fruit peel extract

Primary Polyphenols / Flavonoids

Oleoresin

Limonoids

Quercetin

Rutin

Scopoletin

Source:
https://www.tandfonline.com/doi/full/10.3109/13880209.2012.682116
https://www.mdpi.com/2072-6643/7/8/5312/htm

Determination of Free Radical Scavenging, Antioxidative DNA Damage Activities and Phytochemical Components of Active Fractions fromLansium domesticum Corr. Fruit

“The peel of L. domesticum fruits possessed higher O₂^−• and OH^• scavenging activity than the seeds, particularly when extracted with 50% aqueous ethanol and partitioned with ethyl acetate (LDSK50-EA). This fraction had high potential of both hydrophilic and lipophilic antioxidants. Moreover, LDSK50-EA had a geno-protective effect by reduction of the DNA damage induced by H₂O₂ radicals, proven by comet assay in TK6 cells. This study generated new and updated information on the biological activity of extracts of long-kong fruits. It may lead to a discovery of new alternative sources of natural antioxidant and anti-genotoxic substances for the prophylaxis or treatment of free radical-related diseases as well as the development of the nutraceutical product industry.”

Mango peel extract (Mangifera indica)

Primary Polyphenols / Flavonoids

Flavonol-O-glycosides

Xanthone-C-glycosides

Quercetin O-glycosides

Kaempferol O-glycoside

Mangiferin

Source:
https://www.sciencedirect.com/science/article/pii/S0308814608002367
https://pubs.acs.org/doi/abs/10.1021/jf030218f

Anti‐diabetic effect of dietary mango (Mangifera indica L.) peel in streptozotocin‐induced diabetic rats

“In the present study, the composition of mango peel powder (MPP) collected from the mango pulp industry was determined and the effect of MPP on ameliorating diabetes and its associated complications was studied.

Mango peel was rich in polyphenols, carotenoids and dietary fibre. Peel extract contained various bioactive compounds and was found to be rich in soluble dietary fibre. Peel extract exhibited antioxidant properties and protected against DNA damage. Therefore, the effect of peel on ameliorating diabetes was investigated in a rat model of diabetes. A significant increase in urine sugar, urine volume, fasting blood glucose, total cholesterol, triglycerides and low density lipoprotein, and decrease in high density lipoprotein were observed in the rats; however, these parameters were ameliorated in diabetic rats fed with diet supplemented with mango peel at 5% and 10% levels in basal diet.

Treatment of diabetic rats with MPP increased antioxidant enzyme activities and decreased lipid peroxidation in plasma, kidney and liver compared to untreated diabetic rats. Glomerular filtration rate and microalbuminuria levels were ameliorated in MPP treated diabetic group.

Mango peel, a by‐product, can be used as an ingredient in functional and therapeutic foods.”

Meyer Lemon peel extract (Citrus × meyeri)

Primary Polyphenols / Flavonoids

Trans-4-hydroxycinnamic acid

5-hydroxy-3,7,3′,4′-tetramethoxyflavone

Tangeretin

Nobiletin

Pentamethylquercetin

Source:
https://www.sciencedirect.com/science/article/pii/S0308814612011326
https://pubs.acs.org/doi/abs/10.1021/acs.jafc.5b02445

Protective effects of lemon flavonoids on oxidative stress in diabetic rats

“The effects of lemon flavonoids, as crude flavonoids prepared from lemon juice, were investigated in diabetic rats. The oxidative stress of eriocitrin (eriodictyol 7‐O‐β‐rutinoside) and hesperidin (hesperetin 7‐O‐β‐rutinoside) on streptozotocin‐induced diabetic rats was investigated. Diabetic rats were given a diet which contained 0.2% crude flavonoids, 0.2% eriocitrin, and 0.2% hesperidin. After the 28‐d feeding period, the concentration of the thiobarbituric acid‐ reactive substance in the serum, liver, and kidney of diabetic rats administered crude flavonoids, eriocitrin, and hesperidin significantly decreased as compared with that of the diabetic group. The levels of 8‐hydroxydeoxyguanosine, which is exchanged from deoxyguanosine owing to oxidative stress, in the urine of diabetic rats administered eriocitrin and hesperidin significantly decreased as compared with that of the diabetic rat group. Crude flavonoids, eriocitrin, and hesperidin suppressed the oxidative stress in the diabetic rats. These results demonstrated that dietary lemon flavonoids of eriocitrin and hesperidin play a role as antioxidant in vivo.”

Momordica charantia fruit peel extract

Primary Polyphenols / Flavonoids

Catechin

Caffeic acid

Gallic acid

β-carotene

Mormodicoside

Source:
https://www.sciencedirect.com/science/article/pii/S0308814608002793
http://www.ijournalhs.org/article.asp?issn=2542-6214;year=2014;volume=7;issue=2;spage=113;epage=117;aulast=Sen

Modulation of xenobiotic metabolism and oxidative stress in chronic streptozotocin‐induced diabetic rats fed with Momordica charantia fruit extract

“We studied the long‐term effects of streptozotocin‐induced diabetes on tissue‐specific cytochrome P450 (CYP) and glutathione‐dependent (GSH‐dependent) xenobiotic metabolism in rats. In addition, we also studied the effect of antidiabetic Momordica charantia (karela) fruit‐extract feeding on the modulation of xenobiotic metabolism and oxidative stress in rats with diabetes. Our results have indicated an increase (35–50%) in CYP4A‐dependent lauric acid hydroxylation in liver, kidney, and brain of diabetic rats. About a two‐fold increase in CYP2E‐dependent hepatic aniline hydroxylation and a 90–100% increase in CYP1A‐dependent ethoxycoumarin‐O‐deethylase activities in kidney and brain were also observed. A significant increase (80%) in aminopyrene N‐demethylase activity was observed only in rat kidney, and a decrease was observed in the liver and brain of diabetic rats.

A significant increase (77%) in NADPH‐dependent lipid peroxidation (LPO) in kidney of diabetic rats was also observed. On the other hand, a decrease in hepatic LPO was seen during chronic diabetes. During diabetes an increased expression of CYP1A1, CYP2E1, and CYP4A1 isoenzymes was also seen by Western blot analysis. Karela‐juice feeding modulates the enzyme expression and catalytic activities in a tissue‐ and isoenzyme‐specific manner. A marked decrease (65%) in hepatic GSH content and glutathione S‐transferase (GST) activity and an increase (about two‐fold) in brain GSH and GST activity was observed in diabetic rats. On the other hand, renal GST was markedly reduced, and GSH content was moderately higher than that of control rats. Western blot analyses using specific antibodies have confirmed the tissue‐specific alterations in the expression of GST isoenzymes. Karela‐juice feeding, in general, reversed the effect of chronic diabetes on the modulation of both P450‐dependent monooxygenase activities and GSH‐dependent oxidative stress related LPO and GST activities.

These results have suggested that the modulation of xenobiotic metabolism and oxidative stress in various tissues may be related to altered metabolism of endogenous substrates and hormonal status during diabetes. The findings may have significant implications in elucidating the therapeutic use of antidiabetic drugs and management of Type 1 diabetes in chronic diabetic patients.”

Niihime (Citrus unshiu Citrus tachibana) fruit peel

Primary Polyphenols / Flavonoids

Glycosides

Eriocitrin

Hesperidin

Polymethoxyflavones

Nobiletin

Source:
https://www.jstage.jst.go.jp/article/fstr/12/3/12_3_186/_article/-char/ja/

Isolation of a New Ferulate Derivative from Niihime Fruit, a Sour Citrus Fruit, and Its Antioxidative Activity

“Niihime is a sour Citrus fruit produced along the coast of the Sea of Kumano in the Mie prefecture of Japan. A novel ferulate derivative was isolated from niihime fruit. The structure of the compound was elucidated by spectroscopic analyses and identified as saccharic acid 1,4-lactone 3,5-di-O-ferulate by ¹H-NMR, ¹³C-NMR, and MS analyses. The new compound exhibited significantly higher antioxidative activity than ferulic acid, a parent molecule of the compound, and trolox, a standard antioxidant, as measured by an ORAC assay (P < 0.05). Further, it was abundantly contained in the flavedo, albedo, and segment epidermis of the niihime peel.”

Okra (Abelmoschus esculentus (L.) Moench) peel

Primary Polyphenols / Flavonoids

Carotenoid

Isoflavoneaglycones

Isoquercitrin

Quercetin 3-O-gentiobioside

Myricetin

Source:
https://www.sciencedirect.com/science/article/pii/S0189724115301284
https://www.sciencedirect.com/science/article/abs/pii/S0955286314000515
https://pdfs.semanticscholar.org/63b1/7ee2903c28db69f1cbe61d59c48a22f8eaf7.pdf

Antidiabetic and antihyperlipidemic potential of Abelmoschus esculentus (L.) Moench. in streptozotocin-induced diabetic rats

The present investigation was aimed to study the antidiabetic and antihyperlipidemic potential ofAbelmoschus esculentus peel and seed powder (AEPP and AESP) in streptozotocin (STZ)-induced diabetic rats.

Acute toxicity of AEPP and AESP was studied in rats at 2000 mg/kg dose and diabetes was induced in rats by administration of STZ (60 mg/kg, i.p.). After 14 days of blood glucose stabilization, diabetic rats received AEPP, AESP, and glibenclamide up to 28 days. The blood samples were collected on day 28 to estimate the hemoglobin (Hb), glycosylated hemoglobin (HbA1c), serum glutamate-pyruvate transferase (SGPT), total protein (TP), and lipid profile levels.

In acute toxicity study, AESP and AESP did not show any toxicity or death up to a dose of 2000 mg/kg. Therefore, to assess the antidiabetic action, one by fifth and one by tenth dose of both powders were selected. Administration of AEPP and AESP at 100 and 200 mg/kg dose in diabetic rats showed significant (P < 0.001) reduction in blood glucose level and increase in body weight than diabetic control rats. A significant (P < 0.001) increased level of Hb, TP, and decreased level of HbA1c, SGPT were observed after the treatment of both doses of AEPP and AESP. Also, elevated lipid profile levels returned to near normal in diabetic rats after the administration of AEPP and AESP, 100 and 200 mg/kg dose, compared to diabetic control rats.

The present study results, first time, support the antidiabetic and antihyperlipidemic potential of A. esculentus peel and seed powder in diabetic rats.

Olive leaf (Olea europaea)

Primary Polyphenols / Flavonoids

Luteolin 7-O-glucoside

Oleuropein

Apigenin

Rutin

Apigenin

Source:
https://pubs.acs.org/doi/abs/10.1021/jf903823x
https://onlinelibrary.wiley.com/doi/abs/10.1002/ejlt.200501166

Antidiabetic and Antioxidant Effects of Hydroxytyrosol and Oleuropein from Olive Leaves in Alloxan-Diabetic Rats

“This study was designed to test the antidiabetic and antioxidative activities of olive leaf oleuropein and hydroxytyrosol. Diabetes in Wistar rats was induced by intraperitoneal injections of alloxan. The serum glucose and cholesterol, hepatic glycogen, the thiobarbituric acid-reactive substances (TBARS), and the components of hepatic and serum antioxidant system were examined. Diabetic rats showed hyperglycemia, hypercholesterolemia, increased lipid peroxidation, and depletion in the antioxidant enzymes activities.

The administration, for 4 weeks, of oleuropein and hydroxytyrosol rich extracts, leading to 8 and 16 mg/kg body weight of each compound, significantly decreased the serum glucose and cholesterols levels and restored the antioxidant perturbations. These results suggested that the antidiabetic effect of oleuropein and hydroxytyrosol might be due to their antioxidant activities restraining the oxidative stress which is widely associated with diabetes pathologies and complications.”

Onion peel extract (Allium cepa)

Primary Polyphenols / Flavonoids

Quercetin

Delphinidin

Quercetin 4′-O--glucopyranoside

Kaempferol

Protocatechuic acids

Source:
https://pubs.acs.org/doi/abs/10.1021/jf011102r
http://www.academicjournals.org/app/webroot/article/article1380382031_AbouZid%20and%20Elsherbeiny.pdf
https://www.sciencedirect.com/science/article/pii/S0278691509000702

Onion peel extracts ameliorate hyperglycemia and insulin resistance in high fat diet/streptozotocin-induced diabetic rats

“Quercetin derivatives in onions have been regarded as the most important flavonoids to improve diabetic status in cells and animal models. The present study was aimed to examine the hypoglycemic and insulin-sensitizing capacity of onion peel extract (OPE) containing high quercetin in high fat diet/streptozotocin-induced diabetic rats and to elucidate the mechanism of its insulin-sensitizing effect.

Male Sprague-Dawley rats were fed the AIN-93G diet modified to contain 41.2% fat and intraperitoneally injected with a single dose of streptozotocin (40 mg/kg body weight). One week after injection, the rats with fasting blood glucose levels above 126 mg/dL were randomly divided into 4 groups to treat with high fat diet containing 0 (diabetic control), 0.5, or 1% of OPE or 0.1% quercetin (quercetin equivalent to 1% of OPE) for 8 weeks. To investigate the mechanism for the effects of OPE, we examined biochemical parameters (insulin sensitivity and oxidative stresses) and protein and gene expressions (pro-inflammatory cytokines and receptors).

Compared to the diabetic control, hypoglycemic and insulin-sensitizing capability of 1% OPE were demonstrated by significant improvement of glucose tolerance as expressed in incremental area under the curve (P = 0.0148). The insulin-sensitizing effect of OPE was further supported by increased glycogen levels in liver and skeletal muscle (P < 0.0001 and P = 0.0089, respectively). Quantitative RT-PCR analysis showed increased expression of insulin receptor (P = 0.0408) and GLUT4 (P = 0.0346) in muscle tissues. The oxidative stress, as assessed by superoxide dismutase activity and malondialdehyde formation, plasma free fatty acids, and hepatic protein expressions of IL-6 were significantly reduced by 1% OPE administration (P = 0.0393, 0.0237, 0.0148 and 0.0025, respectively).

OPE might improve glucose response and insulin resistance associated with type 2 diabetes by alleviating metabolic dysregulation of free fatty acids, suppressing oxidative stress, up-regulating glucose uptake at peripheral tissues, and/or down-regulating inflammatory gene expression in liver. Moreover, in most cases, OPE showed greater potency than pure quercetin equivalent. These findings provide a basis for the use of onion peel to improve insulin insensitivity in type 2 diabetes.”

Pear peel extracts (Pyrus spp.)

Primary Polyphenols / Flavonoids

β-carotene

Glycoside

Isorhamnetin

Malaxinic acid

Epicatechin

Source:
https://pubs.acs.org/doi/abs/10.1021/jf030137j
https://www.mdpi.com/2076-3921/2/2/37
https://link.springer.com/article/10.1007/s10068-013-0148-z

Anti-diabetic activity in type 2 diabetic mice and α-glucosidase inhibitory, antioxidant and anti-inflammatory potential of chemically profiled pear peel and pulp extracts (Pyrus spp.)

“Total phenolic acids, total flavonoids, total triterpenes contents, and eleven monomeric compounds, derived from eight different pears’ peel and pulp, were qualitatively and quantitively profiled utilizing HPLC and HPLC-MS. All the chemical components found in the peel were approximately 2 to 18 folds concentrated than those in the pulp. Their antioxidant (reducing power and 2, 2-diphenyl-1-picrylhydrazyl/DPPH assay) and anti-inflammatory (xylene-induced mouse ear edema assay) activities were comparatively evaluated. Correlation analysis and principal component analysis were utilized to seek bioactive components in antioxidant and anti-inflammatory activities.

Subsequently, Yaguang pear (Pyrus ussuriensis Maxim, with high polyphenols content) was selected to investigate in vitroand in vivo anti-diabetic potential (α-glucosidase inhibition assay and hypoglycemic assay in streptozocin-induced type 2 diabetic mice). Eleven monomeric compounds were seriatim examined for α-glucosidase inhibitory activity to fish out anti-diabetic components. For the first time, this study delineated pear peel’s anti-diabetic prospect of treatment for type 2 diabetes.”

Persimmon peel extract

Primary Polyphenols / Flavonoids

Glycosides

Isoquercitrin

Hyperin

Epigallocatechin

β-carotene

Source:
https://www.jstage.jst.go.jp/article/bpb/33/1/33_1_122/_article/-char/ja/
https://www.sciencedirect.com/science/article/pii/S0308814610013142
https://www.tandfonline.com/doi/full/10.1080/10942912.2012.731460

Protective effect of persimmon peel polyphenol against high glucose-induced oxidative stress in LLC-PK₁ cells

“The effect of persimmon peel polyphenol (PPP) on high glucose-induced oxidative stress was investigated using LLC-PK₁ cells, which is susceptible to oxidative stress. High-concentration glucose (30 mM) treatment induced LLC-PK₁ cell death, but high molecular-PPP (HMPPP) and low molecular-PPP (LMPPP), at concentrations of 5 or 10 μg/ml, significantly inhibited the high glucose-induced cytotoxicity. Furthermore, treatment with HMPPP or LMPPP dose-dependently reduced the intracellular reactive oxygen species level increased by 30 mM glucose. In addition, nitric oxide, superoxide and peroxynitrite levels were increased by 30 mM glucose treatment, but they were concentration-dependently inhibited by HMPPP or LMPPP treatment.

High glucose levels induced the overexpressions of inducible nitric oxide synthase (iNOS) and cyclooxygenase-2 (COX-2) proteins, but HMPPP or LMPPP treatment reduced the overexpressions of these proteins. HMPPP or LMPPP also inhibited the nuclear translocation of nuclear factor-kappa B (NF-κB) induced by 30 mM glucose in LLC-PK₁ cells. In particular, LMPPP exhibited stronger inhibitory activities on high glucose induced oxidative stress than HMPPP. These findings indicate the potential benefits of persimmon peel as a valuable source of antioxidants in the diabetic condition which will reduce the oxidative stress induced by hyperglycemia.”

Petroselinum crispum extract

Primary Polyphenols / Flavonoids

Apigenin

Isorhamnetin

Kaempferol

Luteolin

Quercetin

Source:
https://www.sciencedirect.com/science/article/pii/S0308814601001145

Effects of parsley (Petroselinum crispum) on the liver of diabetic rats: a morphological and biochemical study

“Parsley is used by diabetics in Turkey to reduce blood glucose. The present study aims to investigate both the morphological and biochemical effects of parsley on liver tissue. Rat hepatocytes were examined by light and electron microscopy. Degenerative changes were observed in the hepatocytes of diabetic rats. These degenerative changes were significantly reduced or absent in the hepatocytes of diabetic rats treated with parsley. Blood glucose levels, alanine transaminase and alkaline phosphatase were observed to be raised in diabetic rats. Diabetic rats treated with parsley demonstrated significantly lower levels of blood glucose, alanine transaminase and alkaline phosphatase. The present study suggests that parsley demonstrates a significant hepatoprotective effect in diabetic rats.”

Pineapple (Ananas cosmosus) peel extract

Primary Polyphenols / Flavonoids

Catechin

Epicatechin

Ferulic acid

β-carotene-linoleate

Carotenoids

Source:
https://www.tandfonline.com/doi/full/10.1080/10942912.2012.732168
https://www.sciencedirect.com/science/article/abs/pii/S0963996910004801
http://en.cnki.com.cn/Article_en/CJFDTotal-SPYK201009067.htm

ANTIOXIDANT EFFECT OF PINEAPPLE (ANANAS COSMOSUS) PEEL EXTRACT ON ALCOHOL‐INDUCED OXIDATIVE STRESS IN SPLENIC TISSUES OF MALE ALBINO RATS

“Oxidative stress was induced by oral administration of ethanol (20% w/v) at a dosage of 5 mL/kg body weight in rats. After 28 days of treatment, the rats were fasted overnight and sacrificed by cervical dislocation. Splenic tissue homogenates were used for the assessment of protein concentration, reduced glutathione (GSH), catalase, superoxide dismutase (SOD) and lipid peroxidation. Feeding on alcohol caused a significant decrease in GSH level in the group fed alcohol only, while treatment with pineapple peel extracts increased the GSH activities. No significant difference was observed in SOD levels of the negative control and group fed on only pineapple peel extract. There was an elevated catalase activity in the negative control.

Pineapple peel extract significantly reduced it. Treatment with pineapple peel extracts was observed to reduce malondialdehyde (MDA) in alcohol‐fed groups. Protein concentration increased after treatment with the extracts. This study indicates the protective effect of pineapple peel extract against alcohol‐induced oxidative stress.”

Pomegranate peel extract (Punica granatum )

Primary Polyphenols / Flavonoids

Rutin

Catechin

Proanthocyanidins

Cyanidin-3-glucoside

Tannic acid

Source:
http://citeseerx.ist.psu.edu/viewdoc/download?doi=10.1.1.849.3158&rep=rep1&type=pdf
https://academicjournals.org/journal/JMPR/article-full-text-pdf/A0B26C529029

Medicinal Values of Fruit Peels from Citrus sinensis, Punica granatum, and Musa paradisiacawith Respect to Alterations in Tissue Lipid Peroxidation and Serum Concentration of Glucose, Insulin, and Thyroid Hormones

“Peel extracts from Citrus sinensis, Punica granatum, and Musa paradisiaca were investigated for their effects on tissue lipid peroxidation (LPO) and on the concentration of thyroid hormones, insulin, and glucose in male rats. In vitro inhibition of H₂O₂-induced LPO in red blood cells of rats by 0.25, 0.50, 1.0, and 2.0 μg/mL C. sinensis, P. granatum, and M. paradisiacapeel extracts was observed in a dose-specific manner. Maximum inhibition was observed at 0.50 μg/mL C. sinensis, 2.0μg/mL P. granatum, and 1.0 μg/mL M. paradisiaca. In the in vivo investigation, out of four different concentrations of each peel extract, 25, 200, and 100 mg/kg C. sinensis, P. granatum, and M. paradisiaca, respectively, were found to maximally inhibit hepatic LPO.

The most effective doses were further evaluated for effects on serum triiodothyronine (T₃), thyroxine (T₄), insulin, and glucose concentrations. C. sinensis exhibited antithyroidal, hypoglycemic, and insulin stimulatory activities, in addition to inhibition of LPO, as it significantly decreased the serum T₄ (P < .05) and glucose (P < .001) concentrations with a concomitant increase in insulin levels (P < .05). P. granatum decreased LPO in hepatic, cardiac, and renal tissues (P < .01, P < .001, and P < .05, respectively) and serum glucose concentration (P < .01). M. paradisiaca strongly inhibited the serum level of thyroid hormones (P < .01 for both T₃ and T₄) but increased the level of glucose (P < .05).

These findings reveal the hitherto unknown potential of the tested peel extracts in the regulation of thyroid function and glucose metabolism. Besides antiperoxidative activity, C. sinensis extract has antithyroidal, hypoglycemic, and insulin stimulatory properties, which suggest its potential to ameliorate both hyperthyroidism and diabetes mellitus.”

Pomelo (citrus maxima) peel

Primary Polyphenols / Flavonoids

Hesperidin

Naringin

Eriocitrin

Didymin

Maringin

Source:
https://europepmc.org/article/cba/486719
https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0077915

Extracts of Pomelo Peels Prevent High-Fat Diet-Induced Metabolic Disorders in C57BL/6 Mice through Activating the PPARα and GLUT4 Pathway

“Metabolic syndrome is a serious health problem in both developed and developing countries. The present study investigated the anti-metabolic disorder effects of different pomelo varieties on obese C57BL/6 mice induced by high-fat (HF) diet.

The peels of four pomelo varieties were extracted with ethanol and the total phenols and flavonoids content of these extracts were measured. For the animal experiment, the female C57BL/6 mice were fed with a Chow diet or a HF diet alone or supplemented with 1% (w/w) different pomelo peel extracts for 8 weeks. Body weight and food intake were measured every other day. At the end of the treatment, the fasting blood glucose, glucose tolerance and insulin (INS) tolerance test, serum lipid profile and insulin levels, and liver lipid contents were analyzed. The gene expression analysis was performed with a quantitative real-time PCR assay.

The present study showed that the Citrus grandis liangpinyou (LP) and beibeiyou (BB) extracts were more potent in anti-metabolic disorder effects than the duanshiyou (DS) and wubuyou (WB) extracts. Both LP and BB extracts blocked the body weight gain, lowered fasting blood glucose, serum TC, liver lipid levels, and improved glucose tolerance and insulin resistance, and lowered serum insulin levels in HF diet-fed mice. Compared with the HF group, LP and BB peel extracts increased the mRNA expression of PPARα and its target genes, such as FAS, PGC-1α and PGC-1β, and GLUT4 in the liver and white adipocyte tissue (WAT).

We found that that pomelo peel extracts could prevent high-fat diet-induced metabolic disorders in C57BL/6 mice through the activation of the PPARα and GLUT4 signaling. Our results indicate that pomelo peels could be used as a dietary therapy and the potential source of drug for metabolic disorders.”

Potato Peel extract

Primary Polyphenols / Flavonoids

Quercetin

Caffeic acid

Aesculetin

Scopoletin

Pelagonidin

Source:
https://onlinelibrary.wiley.com/doi/abs/10.1002/jsfa.2740100209
https://onlinelibrary.wiley.com/doi/abs/10.1002/(SICI)1097-0010(199805)77:1%3C45::AID-JSFA1%3E3.0.CO;2-S

Protective Effect of Potato Peel Powder in Ameliorating Oxidative Stress in Streptozotocin Diabetic Rats

“The potential of dietary potato peel (PP) powder in ameliorating oxidative stress (OS) and hyperglycemia was investigated in streptozotocin (STZ)-induced diabetic rats. In a 4-week feeding trial, incorporation of potato peel powder (5 and 10%) in the diet of diabetic rats was found to significantly reduce the plasma glucose level and also reduce drastically the polyuria of STZ diabetic rats. The total food intake was significantly reduced in the diabetic rats fed 10% PP powder compared to the control diabetic rats. However, the body weight gain over 28 days was nearly four times greater in PP powder supplemented diabetic rats (both at 5 and 10%) compared to the control diabetic rats. PP powder in the diet also decreased the elevated activities of serum transaminases (ALT and AST) and nearly normalized the hepatic MDA and GSH levels as well as the activities of specific antioxidant enzymes in liver of diabetic rats.

The result of these studies clearly establishes the modulatory propensity of PP against diabetes induced alterations. Considering that potato peels are discarded as waste and not effectively utilized, these results suggest the possibility that PP waste could be effectively used as an ingredient in health and functional food to ameliorate certain disease states such as diabetes.”

Psidium guajava raw fruit peel extract

Primary Polyphenols / Flavonoids

Quercetin

Kaempferol

Guajaverin

β‐sitosterol glucoside

Ferulic acid

Source:
https://onlinelibrary.wiley.com/doi/full/10.1111/j.1365-2184.2011.00797.x

Anti-hyperglycaemic potential of Psidium guajava raw fruit peel

“This study was undertaken to evaluate the glycaemic potential of aqueous extract of Psidium guajava unripe fruit peel on blood glucose level (BGL) of normal and streptozotocin induced mild and severely diabetic rats as an extension of our previous work carried out on Psidium guajava ripe fruit peel.

The aqueous extract of P. guajava unripe fruits was prepared. Male 6-8 wk old albino Wistar rats were selected for the experiments. Diabetes was induced by streptozotocin infection. Blood glucose levels were measured by glucose oxidase method. Antihyperglycaemic activity of the extract was assessed in mild and severely diabetic rats.

The maximum fall of 21.2 per cent (P<0.01) and 26.9 per cent (P<0.01) after 3 h of glucose administration during glucose tolerance test (GTT) was observed in BGL from a dose of 400 mg/kg, identified as the most effective dose, in normal and mild diabetic rats respectively. In severely diabetic rats the maximum fall of 20.8 and 17.5 per cent in fasting blood glucose (FBG) and post prandial glucose (PPG) levels, and 50 per cent (P<0.01) in urine sugar levels was observed with the same dose. Haemoglobin level increased by 5.2 per cent (P<0.05) and body weight by 2.5 per cent (P<0.05) after 21 days treatment.

Normal, mild and severely diabetic rat models had shown hypoglycaemic as well as antidiabetic effect of the unripe guava fruit peel aqueous extract. Further studies need to be done to characterize the active components of the peel.”

Purple passion fruit peel extract

Primary Polyphenols / Flavonoids

Cyanidin-3-O-glucoside

Quercetin-3-O-glucoside

Edulilic acid

Cyanidin-3-O-glucoside

Kampferol-3-O-glucoside

Source:
https://journals.sagepub.com/doi/full/10.1177/2156587213475627

Efficacy of Purple Passion Fruit Peel Extract in Lowering Cardiovascular Risk Factors in Type 2 Diabetic Subjects

The clinical efficacy of purple passion fruit peel extract (a flavonoid-rich dietary supplement) in reducing cardiovascular risk factors in adult type 2 diabetic subjects was investigated in a randomized, double-blind, placebo-controlled trial. Forty-one subjects were randomly assigned to receive a daily dose of purple passion fruit (220 mg) or a matched placebo for 16 weeks. Body mass index, blood pressure, fasting and postprandial blood glucose, glycated hemoglobin, and lipid profile were determined at baseline and at monthly intervals. A significant reduction in systolic blood pressure and fasting blood glucose was observed following administration of purple passion fruit (P<.05).

Purple passion fruit was well tolerated, and no adverse events were reported. These data suggest that purple passion fruit supplementation for 16 weeks in type 2 diabetics results in a significant reduction in systolic blood pressure and fasting blood glucose, indicating that purple passion fruit is safe and well tolerated by diabetics.

Quince (Cydonia oblonga Miller) peel extract

Primary Polyphenols / Flavonoids

3-, 4-, and 5-O-caffeoylquinic acids

3,5-dicaffeoylquinic acid

Quercetin glycoside

Rutin

Kampferol-3-O-glucoside

Source:
https://pubs.acs.org/doi/abs/10.1021/jf0203139

Quince (Cydonia oblonga Miller) peel polyphenols modulate LPS-induced inflammation in human THP-1-derived macrophages through NF-κB, p38MAPK and Akt inhibition

“Chronic inflammation is a hallmark of several pathologies, such as rheumatoid arthritis, gastritis, inflammatory bowel disease, atherosclerosis and cancer. A wide range of anti-inflammatory chemicals have been used to treat such diseases while presenting high toxicity and numerous side effects. Here, we report the anti-inflammatory effect of a non-toxic, cost-effective natural agent, polyphenolic extract from the Tunisian quince Cydonia oblongaMiller. Lipopolysaccharide (LPS) treatment of human THP-1-derived macrophages induced the secretion of high levels of the pro-inflammatory cytokine TNF-α and the chemokine IL-8, which was inhibited by quince peel polyphenolic extract in a dose-dependent manner. Concomitantly, quince polyphenols enhanced the level of the anti-inflammatory cytokine IL-10 secreted by LPS-treated macrophages.

We further demonstrated that the unexpected increase in IL-6 secretion that occurred when quince polyphenols were associated with LPS treatment was partially responsible for the polyphenols-mediated inhibition of TNF-α secretion. Biochemical analysis showed that quince polyphenols extract inhibited the LPS-mediated activation of three major cellular pro-inflammatory effectors, nuclear factor-kappa B (NF-κB), p38MAPK and Akt. Overall, our data indicate that quince peel polyphenolic extract induces a potent anti-inflammatory effect that may prove useful for the treatment of inflammatory diseases and that a quince-rich regimen may help to prevent and improve the treatment of such diseases.”

Rambutan (Nephelium lappaceum L.) Peel Extract

Primary Polyphenols / Flavonoids

Gallic Acid

Geraniin

Corilagin

Hederagenin

Arabinopyranoside

Source:
https://scialert.net/fulltextmobile/?doi=rjphyto.2017.42.47

Protective effects of rambutan (Nephelium lappaceum) peel phenolics on H₂O₂-induced oxidative damages in HepG2 cells and d-galactose-induced aging mice

“Rambutan peel phenolic (RPP) extracts were prepared via dynamic separation with macroporous resin. The total phenolic content and individual phenolics in RPP were determined. Results showed that the total phenolic content of RPP was 877.11 mg gallic acid equivalents (GAE)/g extract. The content of geranin (122.18 mg/g extract) was the highest among those of the 39 identified phenolic compounds. RPP protected against oxidative stress in H₂O₂-induced HepG2 cells in a dose-response manner. The inhibitory effects of RPP on cell apoptosis might be related to its inhibitory effects on the generation of intracellular reactive oxygen species and increased effects on superoxide dismutase activity. The in vivo anti-aging activity of RPP was evaluated using an aging mice model that was induced by d-galactose (d-gal). The results showed that RPP enhanced the antioxidativestatus of experimental mice. Moreover, histological analysis indicated that RPP effectively reduced d-gal-induced liver and kidney tissue damage in a dose-dependent manner. Therefore, RPP can be used as a natural antioxidant and anti-aging agent in thepharmaceutical and food industries.”

Satsuma Mandarin peel extract (CitruS unshiu)

Primary Polyphenols / Flavonoids

Glucopyranosylphloretin

Phloridzin

Aglycon

Chalcone

Narirutin

Source:
https://www.sciencedirect.com/science/article/abs/pii/S0031942201001327
https://onlinelibrary.wiley.com/doi/abs/10.1034/j.1399-3054.2001.1110109.x
https://www.sciencedirect.com/science/article/abs/pii/S0925521412002104

Lipolysis induced by segment wall extract from Satsuma mandarin orange

“The lipolysis induced by Satsuma mandarin orange (Citrus unshu Mark) was investigated using rat fat cells. Peel or segment wall extract from Satsuma mandarin orange induced the lipolysis in a concentration-dependent manner, whereas juice sac extract did not induce the lipolysis. High concentration of synephrine, which is an adrenergic amine, was detected in the peel or segment wall extract, whereas it was not detected in the juice sac extract.

The segment wall extracts from Iyokan and orange had high lipolytic activity, whereas the extracts from grapefruit and lemon did not have lipolytic activity. The beta-antagonist inhibited the lipolysis elicited by the segment wall extract from Satsuma mandarin orange, whereas alpha-antagonist did not inhibit the lipolysis induced by the segment wall. The lipolysis induced by the segment wall was considerably higher in the visceral fat cells when compared to the subcutaneous fat cells. These results suggest that the segment wall, an edible fraction, from Satsuma mandarin orange might be useful as a functional food, especially as a fat-reducing material.”

Scutellaria laterifolia

Primary Polyphenols / Flavonoids

Baicalein

Baicalin

Glutamine

Aglycones

Scutellarin

Source:
https://www.sciencedirect.com/science/article/abs/pii/S0944711304702767
https://pubs.acs.org/doi/abs/10.1021/jf048408t
https://www.thieme-connect.com/products/ejournals/html/10.1055/s-2008-1034358

New therapeutic aspects of flavones: The anticancer properties of Scutellaria and its main active constituents Wogonin, Baicalein and Baicalin

“Traditional Chinese medicines have been recently recognized as a new source of anticancer drugs and new chemotherapy adjuvant to enhance the efficacy of chemotherapy and to ameliorate the side effects of cancer chemotherapies however their healing mechanisms are still largely unknown. Scutellariabaicalensis is one of the most popular and multi-purpose herb used in China traditionally for treatment of inflammation, hypertension, cardiovascular diseases, and bacterial and viral infections. Accumulating evidence demonstrate that Scutellariaalso possesses potent anticancer activities. The bioactive components of Scutellaria have been confirmed to be flavones. The major constituents of Scutellaria baicalensis are Wogonin, Baicalein and Baicalin. These phytochemicals are not only cytostatic but also cytotoxic to various human tumor cell lines in vitro and inhibit tumor growth in vivo.

Most importantly, they show almost no or minor toxicity to normal epithelial and normal peripheral blood and myeloid cells. The antitumor functions of these flavones are largely due to their abilities to scavenge oxidative radicals, to attenuate NF-κB activity, to inhibit several genes important for regulation of the cell cycle, to suppress COX-2 gene expression and to prevent viral infections. The tumor-selectivity of Wogonin has recently been demonstrated to be due to its ability to differentially modulate the oxidation–reduction status of malignant vs. normal lymphocytic cells and to preferentially induce phospholipase Cγ1, a key enzyme involved in Ca²⁺ signaling, through H₂O₂ signaling in malignant lymphocytes. This review is aimed to summarize the research results obtained since the last 20 years and to highlight the recently discovered molecular mechanisms.”

Sweet Orange peel extract (Citrus sinensis)

Primary Polyphenols / Flavonoids

C‐glycosylated ﬂavones

Polymethoxylated

O‐glycosylated

6‐C‐β‐glucosyldiosmin

6,8‐di‐C‐β‐glucosyldiosmin

Source:
https://onlinelibrary.wiley.com/doi/abs/10.1002/bmc.430

ORANGE: RANGE OF BENEFITS

“Orange (citrus sinensis) is well known for its nutritional and medicinal properties throughout the world. From times immemorial, whole Orange plant including ripe and unripe fruits, juice, orange peels, leaves and flowers are used as a traditional medicine. Citrus sinensis belongs to the family Rutaceae. The fruit is a fleshy, indehiscent, berry that ranges widely in size from 4 cm to 12 cm. The major medicinal properties of orange include anti-bacterial, anti-fungal, anti- diabetic, cardio- protective, anti-cancer, anti-arthritic, anti-inflammatory, antioxidant, anti-Tubercular, anti-asthmatic and anti-hypertensive. Phytochemically, whole plant contains limonene, citral, neohesperidin, naringin, rutin, rhamnose, eriocitrin, and vitamin-C. In the present review article, a humble attempt is made to compile all the strange facts available About this tasty fruit.

Anti-diabetic activity of orange is due to bioflavonoids such as hesperidin and naringin present in citrus fruit peels. These peels play an anti-diabetic rolein C57BL/Ks J-db/db mice via regulation of glucose regulatory enzymes. They decrease the activity of glucose-6-phosphatase and phosphoenol pyruvate. The anti-diabetic potential of orange peel and juice appear to be mediated via anti peroxidation, inhibition of α-amylase enzyme activity that is responsible for the conversion of complex carbohydrates to glucose, increased hepatic glycogen content, stimulation of insulin secretion, and repair of secretory defects of pancreatic β-cells [18,19].”

Syzygium cumini Skeels extract

Primary Polyphenols / Flavonoids

Glucoside

Ellagic acid

Isoquercetin

Kaemferol

Myrecetin

Source:
https://www.sciencedirect.com/science/article/pii/S2221169112600501

Syzygium cumini (L.) Skeels: A review of its phytochemical constituents and traditional uses

“Syzygium cumini (S. cumini) (L.) Skeels (jambolan) is one of the widely used medicinal plants in the treatment of various diseases in particular diabetes. The present review has been primed to describe the existing data on the information on botany, phytochemical constituents, traditional uses and pharmacological actions of S. cumini (L.) Skeels (jambolan). Electronic database search was conducted with the search terms of Eugenia jambolana, S. cumini, jambolan, common plum and java plum. The plant has been viewed as an antidiabetic plant since it became commercially available several decades ago. During last four decades, numerous folk medicine and scientific reports on the antidiabetic effects of this plant have been cited in the literature. The plant is rich in compounds containing anthocyanins, glucoside, ellagic acid, isoquercetin, kaemferol and myrecetin.

The seeds are claimed to contain alkaloid, jambosine, and glycoside jambolin or antimellin, which halts the diastatic conversion of starch into sugar. The vast number of literatures found in the database revealed that the extracts of different parts of jambolan showed significant pharmacological actions. We suggest that there is a need for further investigation to isolate active principles which confer the pharmacological action. Hence identification of such active compounds is useful for producing safer drugs in the treatment of various ailments including diabetes.”

Tangerine peel extract (Citrus reticulata)

Primary Polyphenols / Flavonoids

Hesperidin

Nobiletin

Tangeretin

Nobiletin

Sinensetin

Source:
https://www.sciencedirect.com/science/article/pii/S0278691514002890
https://pubs.acs.org/doi/abs/10.1021/jf960110i

Effect of Citrus Flavonoids, Naringin and Naringenin, on Metabolic Syndrome and Their Mechanisms of Action

“Naringin and naringenin supplementation has proven to be efficacious for the treatment of metabolic syndrome and obesity in animal models (60, 111). The dose used in animal studies may not be achieved in human trials, however, and emphasis should be given to establish a dietary recommendation of citrus fruit consumption or for the pure compound naringin. Most of naringin’s observed biologic activities are related in some part to its potent antioxidant nature. However, several other molecular signaling pathways modified by naringin were also revealed recently. In metabolic syndrome, obesity, and related cardiovascular complications, naringin influences AMPK-, PPARα–, and CPT-1–mediated fat utilization and preserves mitochondrial function.

Moreover, naringin also prevents the TNF-α–mediated inflammatory process and tissue damage in liver and vasculature. Figure 3 shows a proposed mechanism for increased mitochondrial biogenesis by naringin. Another consideration for oral administration of naringenin/naringin should be the contraindications of taking certain drugs such as statins and calcium channel blockers because of the inhibitory effects on intestinal CYP450 enzymes. Moreover, further clinical investigations should be carried out with naringin in metabolic diseases.”

Tomato (Solanum lycopersicum L.) peel extract

Primary Polyphenols / Flavonoids

Quercetin

Naringenin

Kaempferol

Rutinoside

Isoquercitrin

Source:
https://academic.oup.com/jxb/article/53/377/2099/497208

DNA and mitochondrial protective effect of lycopene rich tomato (Solanum lycopersicum L.) peel extract prepared by enzyme assisted extraction against H₂O₂ induced oxidative damage in L6 myoblasts

“Lycopene rich extracts (ETE) were prepared by enzyme assisted extraction of tomato peel. Oxidative damage was induced in L6 myoblasts by exposing cells to H₂O₂ in presence and absence (control) of ETE. The potential of ETE to protect cells from oxidative damage was investigated in terms of cytotoxicity (MTT assay), Reactive oxygen species (ROS) by 2′, 7′-dichlorofluorescindiacetate (H₂DCFDA), DNA damage (ladder assay, 8-oxo-dG), Hoechst 33342 nuclear staining, mitochondrial stability by ATP production and mitochondrial membrane potential by Rhodamine 123 staining.

It was observed that treatment of cells with ETE significantly increased cell viability, decreased ROS production, reduced DNA fragmentation, chromatin condensation & 8-oxo-dG, increased ATP levels and mitochondrial membrane potential. Results indicated that ETE could protect cells from H₂O₂ induced oxidative damage significantly as compared to control. These results depicted the antioxidant potential of tomato peel extract which can counteract the redox imbalance in cells induced by oxidative stress condition.”

Trapa natans fruit peel extract

Primary Polyphenols / Flavonoids

Rutin

Trapain

Euginin

1,2,3,6-tetra-O-galloyl-beta-D-glucopyranose

Quercetin

Source:
https://www.tandfonline.com/doi/full/10.1080/19476337.2014.992967

Antidiabetic Activity of Trapa natans Fruit Peel Extract Against Streptozotocin Induced Diabetic Rats

“Trapa natans L. (Lythraceae), commonly known as Water Chestnut in English, is an annual aquatic floating herb occurring throughout the Indian subcontinent and used traditionally for several medicinal purposes. The present study was aimed to evaluate antidiabetic activity of methanol extract of T. napans fruit peels (METN) in Wistar rats. The effect of METN on oral glucose tolerance and its effect on normoglycemic rats were studied. Diabetes mellitus was induced in rats by single intraperitonial injection of streptozotocin (STZ, 65 mg/kg body weight). Three days after STZ induction, the hyperglycemic rats were treated with METN orally at the dose of 100 and 200 mg/kg body weight daily for 15 days.

Glibenclamide (0.5 mg/kg b.wt., orally) was used as reference drug. The fasting blood glucose levels were measured on every 5 day during the th 15 days treatment. METN at the dose of 100 and 200 mg/kg orally significantly (p < 0.001) and dose dependently improved oral glucose tolerance, exhibited hypoglycaemic effect in normal rats and antidiabetic activity in STZ-induced diabetic rats by reducing and normalizing the elevated fasting blood glucose levels as compared to those of STZ control group. The present study concludes that T. natans fruit peel demonstrated promising antidiabetic activity in STZ-induced diabetic Wistar rats.”

Wampee (Clausena lansium (Lour.) Skeels) Peel extract

Primary Polyphenols / Flavonoids

Clausenamide

Quercetin

Isorhamnetin

Dihydromyric

2′’,3′’-dihydroxyanisolactone

Source:
https://journals.sagepub.com/doi/abs/10.1177/1934578X1601100502

Antioxidant and anticancer activities of 8-hydroxypsoralen isolated from wampee [Clausena lansium (Lour.) Skeels] peel

“Fruits of wampee [Clausena lansium (Lour.) Skeels] contain a significant amount of coumarins with many health benefits. The activity-guided separation of an ethyl acetate-soluble fraction on a polyamide column followed by silica gel column and high performance liquid chromatography (HPLC) preparation afforded a pure compound, which was identified to be 8-hydroxypsoralen based on the ¹H, ¹³C NMR (nuclear magnetic resonance), and ESI-MS (electrospray ionisation mass spectrometric) analysis.

This isolate exhibited good scavenging activities against DPPH radical and superoxide anion as well as significant reducing power. It also showed potent proliferation inhibitory activity against human hepatocellular liver carcinoma cell line (HepG2), human lung adenocarcinoma epithelial cell line (A549) and human cervical carcinoma cell line (HELA). This is the first report on the antioxidant and cytotoxic properties of C. lansium fruit extract. The food and pharmaceutical industry could be benefited by the usage of this extract containing this constituent.”

Water chestnut (Trapa bispinosa Roxb.) peel

Primary Polyphenols / Flavonoids

Quercetin

Malic acid

Myricetin

Myricitin

2′’,3′’-dihydroxyanisolactone

Source:
https://www.researchgate.net/profile/Lipika_Aidew/publication/280301734_Antimycobacterial_and_Antioxidant_Activities_of_the_Fruit_of_Trapa_natans_L_var_Bispinosa_Reveal_its_Therapeutic_Potential/links/55b055bc08ae11d31039b2fa.pdf
https://www.researchgate.net/profile/Syed_Waheed/publication/305425895_A_comparitive_study_of_antioxidant_properties_and_phytochemical_composition_of_Trapa_bispinosa_Trigonella_foenum-graecum_Syzygium_cumini_and_Betula_utilis/links/5836ad3908aed45931c8024e/A-comparitive-study-of-antioxidant-properties-and-phytochemical-composition-of-Trapa-bispinosa-Trigonella-foenum-graecum-Syzygium-cumini-and-Betula-utilis.pdf

Peel extract of water chestnut (Trapa bispinosa Roxb.) inhibits glycation, degradesα-dicarbonyl compound, and breaks advanced glycation end product crosslinks

“In recent years, glycation in organisms has been positioned as a major risk factor for accelerated aging process, and the concept of glycation stress has gained attention 1). The concept of glycation stress is that the reaction of reducing sugars, aldehydes, etc. with proteins and amino acids produces advanced glycation end products (AGEs), and the accumulation of these substances overloads cells and tissues and disrupts the functioning of functional proteins as well as causes a series of reactions such as induction of inflammation 2). The glycation reaction at the core of glycation stress is a reaction in which proteins and reducing sugars bond nonenzymatically to produce glycation products.

Glycation products that have been identified include the AGEs pentosidine, Nε- (carboxymethyl ) lysine (CML), and pyraline, and their intermediates 3-deoxyglucosone (3DG), glyoxal (GO), and methylglyoxal (MGO) 3). Bioaccumulation of these glycation products is said to be involved in kidney disease and eye disorders associated with progression of diabetes 4), arteriosclerosis 5), osteoporosis 6), Alzheimer’s disease 7), infertility 8), and sclerema 9). Based on these facts, we believe that inhibiting the production and accumulation of glycation products and stimulating the degradation and metabolism of previously produced glycation products will lead to an increased life expectancy, improved quality of life, and disease prevention.

The glycation response inhibiting activity and glycation product degradation activity of the TBE confirm its production inhibitory effect against AGEs and its effect in reducing the amount of accumulated AGEs by degradation of previously produced AGEs. Further, since activities other than antiglycation have been demonstrated, we expect TBE to have wide applications as an anti-aging ingredient. We plan to study its efficacy in humans in the future. The study verified TBE to inhibit glycation product synthesis, degrade α-dicarbonyl compound, and break the AGE crosslinks. The above results suggest that TBE may inhibit production of AGEs and their intermediates and degrade existing α-dicarbonyl compounds and AGE crosslinks in vivo. We expect that TBE may be suitable to reduce glycation stress.”

Yam (Dioscorea alata) peel extract

Primary Polyphenols / Flavonoids

Quercetin

Hesperidin

Apigenin

Dioscorine

Diosgenin

Source:
https://pubs.acs.org/doi/abs/10.1021/jf401864y
http://docsdrive.com/pdfs/medwelljournals/ijmmas/2006/199-203.pdf

Protective effects of the crude extracts from yam (Dioscorea alata) peel on tert-butylhydroperoxide-induced oxidative stress in mouse liver cells

“Researchers have shown that yam extracts contain antioxidative activity; however, there are few reports regarding the antioxidant activities of yam peel. The effects of water and 50% ethanolic extracts from Darsan yam (Dioscorea alata) peel on the oxidative status of tert-butylhydroperoxide (t-BHP)-treated mouse Hepa 1–6 and FL83B liver cell lines were investigated. The cytosols were analysed for H₂O₂ and malondialdehyde (MDA) levels and antioxidative enzymes activities, including superoxide dismutase, glutathione peroxidase (GPx) and catalase activities. Both water and 50% ethanolic extracts from yam peel did not affect cellular MDA level in t-BHP-treated cells, but they altered the level of H₂O₂.

Water extract from yam peel amplified the t-BHP-induced cytotoxicity in Hepa 1–6 whilst the ethanolic extract showed protection in FL83B cells. GPx activity might play an important role in the protective effect associated with t-BHP-induced oxidative stress.”

Yuzu peel extract (Citrus JUNOS)

Yuzu

Primary Polyphenols / Flavonoids

Naringin

Hesperidin

Tangeretin

Phloretin

Eugenol

Source:
https://pdfs.semanticscholar.org/0db2/071e08c0c0074c83a1a67f7807e881f3e080.pdf
https://onlinelibrary.wiley.com/doi/abs/10.1002/1099-1026(200007/08)15:4%3C245::AID-FFJ904%3E3.0.CO;2-V

Citrus junos Tanaka Peel Extract Exerts Antidiabetic Effects via AMPK and PPAR- both In Vitro and In Vivo in Mice Fed a High-Fat Diet

“The antidiabetic effect of the Citrus junos Tanaka (also known as yuja or yuzu) was examined. Ethanol extract of yuja peel (YPEE) significantly stimulated 2-[N-(7-nitrobenz-2-oxa-1,3-diazol-4-yl)amino]-2-deoxy-D-glucose (2-NBDG) uptake in C2C12 myotubes. However, ethanol extract of yuja pulp (YpEE) and water extract of yuja peel (YPWE) or pulp (YpWE) did not stimulate glucose uptake. In addition, peroxisome proliferator-activated receptor gamma (PPAR-) and AMP-activated protein kinase (AMPK) activities were increased by YPEE in a dose-dependent manner. Pretreatment of AMPK inhibitor decreased the glucose uptake stimulated by YPEE in C2C12 myotubes. We confirmed the anti-diabetic effect of YPEE in mice fed a high fat-diet (HFD). Compared with control mice on a normal diet (ND), these mice showed increased body weight, liver fat, insulin resistance, triacylglycerol (TG), and total cholesterol content.

Addition of 5% YPEE significantly reduced the weight gain and rise in liver fat content, serum triacylglycerol (TG), total cholesterol, and insulin resistance found in mice fed a high-fat diet (HFD). Moreover, YPEE reduced the secretion of HFD-induced adipocytokines such as leptin and resistin. YPEE also resulted in increased phosphorylation of AMPK in muscle tissues. These results suggest that ethanol extract of yuja peel exerts anti-diabetic effects via AMPK and PPAR- in both cell culture and mouse models.”

AVAILABLE IN TWO CONCENTRATIONS: 20:1 100g $50 / 200:1 100g $250

Aristotelia chilensi

Primary Polyphenols / Flavonoids

Gentisic acid

Ferulic acid

Gallic acid

p-coumaric acid

Delphinidin

Source:
https://www.sciencedirect.com/science/article/pii/S0308814609009327

Antioxidant and cardioprotective activities of phenolic extracts from fruits of Chilean blackberry Aristotelia chilensis (Elaeocarpaceae), Maqui

In vitro and in vivo anti-diabetic effects of anthocyanins from Maqui Berry (Aristotelia chilensis)

Juice and Phenolic Fractions of the Berry Aristotelia chilensis Inhibit LDL Oxidation in Vitro and Protect Human Endothelial Cells against Oxidative Stress

Size	100g, 400g
Concentration	200:1, 20:1
Blend Type	Regular Blend 200:1, Citrus Only Blend 200:1

32 reviews for PEEL BLEND FLAVONOID POWERHOUSE

Rated 5 out of 5
April – April 20, 2018
QUICK PEEL TESTIMONY ❤
As some of you know I have multiple myeloma and just finished treatment at the end of January and will be starting again in 2 weeks my next cycle.
One of the biggest challenges we face with cancer exhaustion from both the disease and the treatment for it. This last cycle wiped me out more than any other. I have not been able to regain my energy no matter how much I’ve slept, or rested. This is something I have always been able to overcome by adjusting my blends and fasting, but this time was much different.
I found myself begging my drs and Gavin to find something, anything that would give me at least some of my energy back as I was beginning to think I was going to have to stop working….
I received my PEEL blend yesterday 200:1.
This morning I took it at 430 am and left for a 2 hour ride to work. A couple hours ago I looked at my watch and it read 5pm!!!! I can’t believe it. Seriously am in awe that 1 dose, 1/2 tsp on the very 1st day of taking this blend has had such a huge impact on my energy level!!! I took my 2nd dose at 5pm.
I absolutely cannot wait to see what tomorrow and the next few days bring. I am about to get my life back once again because I put my trust and faith in a friend who backs up everything he does with science. Who lays it all out on the table for me to read and research myself (and i do) and without fail… He never let’s me down!!!
Once again Gavin, thank you so much for doing for me naturally what my drs couldn’t do at all!!
#fuckcancer!
Rated 5 out of 5
Rich Ryan – April 25, 2018
Me and my friend are loving this one! More energy and less depression and fatigue. Less for Trinity and Sages to overcome.
Our skin looks better too. Glowing! My body feels like it’s tingling when I go to bed at night. Something in the body that has never been taken care of before is being taken care of now with this Peel blend. Excellent! (Now we know why monkeys eat the whole fruit, peel and all!)
Rated 5 out of 5
Courtney – May 22, 2018
THE INTERSTELLAR PEEL BLEND is rated A++++++++ in my book. After years of living with a painful allergy to the sun, chronic inflammation and insulin sensitivity (that’s a short list of my health issues) I have finally found relief with the INTERSTELLAR PEEL BLEND. I don’t even know where to begin with how happy I am to be able to have such an AMAZINGLY HEALING NATURAL product.
I have a severe allergy to the sun which causes my skin to become unbearably painful, itchy and leaves very dark ugly scars and marks. I also suffer from terrible inflammation that causes me to have severe darkness around my eyes and I wake up in the morning with my eyes so swollen you can hardly see my eyeballs. As the day wears on the swelling would only go down but so much and the darkness never would go away and has only continued to progress further.
But then I I received my FIRST order of PEEL BLEND 200:1!!! I can’t tell you exactly how SHOCKED I was when I woke up that first morning after starting the PEEL BLEND 200:1. I couldn’t believe it, but I had ZERO swelling in my eyes. I thought for sure as the day would wear on the swelling would come back. But no, it stayed unswollen all day. Not only that after a few days of using it I noticed that the darkness around my eyes wasn’t so shocking and was starting to minimize. I can tell that as I continue to use it and my health improves the PEEL BLEND is going to have my eyes back to a healthy state.
As far as my sun allergy leaving dark scars and marks; I noticed within a week I noticed dark scars starting to fade away and I have sun scars that I’ve had for YEARS that have now completely gone away. I can’t explain to anyone how happy that has made me because the scarring was making me very self conscious.
One of the things I truly love is that when I was using regular grocery store citrus peels it was gritty and also they have carbohydrates. But with the Interstellar Peel Blend I can put the scoops into a bottle shake it up and take it with me to have while I’m out and about. It’s not gritty and I don’t have to worry about the extra carbs.
To anyone reading this if you have an opportunity to buy the PEEL BLEND it WILL a greatly improve your health. I don’t have diabetes but I definitely am insulin sensitive and now I can tell if I eat something higher in carbs that because I’m taking the PEEL BLEND I don’t get that brain fog I used to get.
Gavin thank you so much for always being available to answer my questions and for making such amazing natural products. You’re a person of high integrity and your concern for the health of others is truly genuine and heartfelt. You’ve definitely got a customer for life and I will continue to tell others the WHO WHAT WHERE WHEN HOW and WHY my scars are finally going away!
Rated 5 out of 5
Rachel (verified owner) – August 15, 2018
I suffer from cystic acne which is cleared up 90% through a keto diet. I started taking Peel (both citrus and regular) and the changes to my skin were amazing. The remaining acne cleared, wrinkles started filling in, pores disappeared and my skin became softer. If it’s doing this much good for my skin I can only imagine what it’s doing internally.
Rated 5 out of 5
Keith Moon (verified owner) – December 31, 2018
I experienced a noticeable difference in how I processed carbs when taking the peel blends. Although I was limiting carbs in my diet I hadn’t eliminated them enrirely and I still lost body fat as if I was doing a strict Keto diet. I’ve used several different blends over a few years time and really appreciate the quality of these products.
Rated 5 out of 5
Bryan Smith – January 2, 2019
I have struggled with type 2 diabetes since 2012, my blood sugar had been staying above 350 for the past two years or so, and often exceeding 450+.
I started using peer blend back in August and on day zero my blood sugar read 386.
I started taking peel blend 3 times a day. Once in the morning, once in the afternoon and once in the evening.
After 3 days I started to see it come down, day 3 it was down to 310, day 5 of was down to 290. a week later I lowered my dosage to once in the morning at that time my blood sugar read 260, it’s been 5+ months now and my sugar is consistently under 200 and back to feeling great again.
My allergies have been a lot better since I started also.
Rated 5 out of 5
Bryan Smith – January 2, 2019
I have struggled with type 2 diabetes since 2012, my blood sugar had been staying above 350 for the past two years or so, and often exceeding 450+.
I started using peer blend back in August and on day zero my blood sugar read 386.
I started taking peel blend 3 times a day. Once in the morning, once in the afternoon and once in the evening.
After 3 days I started to see it come down, day 3 it was down to 310, day 5 of was down to 290. a week later I lowered my dosage to once in the morning at that time my blood sugar read 260, it’s been 5+ months now and my sugar is consistently under 200 and back to feeling great again.
My allergies have been a lot better since I started also.
Rated 5 out of 5
Dee Dee – January 4, 2019
I LOVE this product. My skin is so much softer since taking it, and my hands and feet are like baby soft. I have had 2 people tell me that I’m reverse aging. I try and follow a keto diet. In the past when I had fallen off the wagon for a day or two I’d gain 4-5 lbs back. Since taking the peel blend I don’t gain it back. It really is a great product.
Rated 5 out of 5
Kathy – January 5, 2019
I really enjoy this product! My skin is looking great and I feel very chill and less anxious since taking Gavin’s blends. I would highly recommend this blend for better looking skin!
Rated 5 out of 5
KD Darby (verified owner) – March 30, 2019
So I first started taking blends when Gavin introduced PEEL in April of 2018 in his Facebook group. He was talking about this amazing combination of ingredients that helped bring down blood sugar readings. As someone with Gestational Diabetes when I had my daughter and also someone whose body shape screamed INSULIN RESISTANT (apple shape with larger middle), I knew I needed to try this blend and begin to regain control of my health. I was already doing daily 22:2 fasts, but my blood sugar readings were still too high. I was on board for trying this new product. I ordered before it even hit the website and had my first PEEL package within a few days. Gavin’s turnaround with orders is crazy fast.
So I tried my first PEEL order. I ordered the 20:1, lower concentration, so I was taking a 1/2 tsp about every 4-6 hours with a swig of water. At first the taste of it gave me the shivers but soon I started loving the flavor – craving it even. At the same time, since I still had my blood sugar monitor from when I had gestational diabetes I decided to keep a more careful eye on my morning blood sugar readings. Within a week it was down 30 points! From about 130 to about 100 in the morning. After another week I was consistently in the 90’s! Okay, I was a believer! But the extra benefits were what kept me taking my PEEL. Suddenly I had more energy to tackle my chore list. And a haze of “blues” (perhaps mild depression) seemed to suddenly lift and my family noticed I was smiling more. In the summer I was feeling so good that I allowed my PEELS to run out, thinking I would be fine. After about a week my husband started asking me what was wrong. I just seemed “down.” I realized the only thing that had changed was my PEEL had run out. Oh geez! Time to reorder and rely on Gavin’s quick shipping!
Since that time I have never let my PEEL run out. If I get close to the end of my jar I reorder to make sure that I don’t have any days without it. My husband is now a believer in how much it helps my energy and mood and even reminds me to take my blends. I added Spice and Pine Pollen to my days and now, from trying the samples Gavin includes in orders at times I am deciding on what next to add. Thermo, Seven Sages and Trinity are all in my next shopping cart! With the encouragement of his Facebook group I have now moved to 44:4 fasting for enhanced insulin resistance healing and my PEEL and SPICE make fasting much easier. Weight is falling off that mid-section and I am moving toward more of an hourglass shape rather than an apple shape. My husband is not only seeing my mood shift but my body shape shift and is becoming a great fan of Interstellar Blends! Blends will be a permanent part of my routine for my physical and mental well-being. I am so happy that I found Gavin, Kristine and all of the research and science that goes with these products.
Rated 5 out of 5
Robert Burnett – April 2, 2019
If we could rate the blends a 10 we would!!
Have been type 2 diabetic for 25 years, until spring 2018 managed to do a reasonable job controlling blood sugars with diet, exercise and prescribed medication. My blood sugar levels had started to not react anymore with medication and Doctor was discussing insulin options.
Under the advice of my daughter (who has taken blends for sometime), , started taking Peel blends and within first week had already noticed a drastic difference in lowering blood sugar levels. Returning 3 months later for doctors visit, after taking Peel blend, she was amazed with my extremely lowered A1C.
My wife and I both take Peel, Trinity and Thermo on a daily basis, the improved overall health benefits from the Interstellar blends have honestly been life changing.
Rated 5 out of 5
Stacy Silva (verified owner) – April 5, 2019
I’ve been taking the blends since 2017. I’m in my late twenties, thin, I don’t fast and I don’t work out. I started because I was starting to think I had chronic fatigue or something. I would get off work in the after noon and take 3-4 hour naps, no energy drink could keep me awake. This is on top of sleeping atleast 9-10 hours at night. I was also feeling extremely emotional, literally ANYTHING could make me cry. I couldn’t look at a picture of a cute animal without bursting into tears. I decided to just spend the money and see what all the fuss was about. Almost immediately I saw a difference. I stopped needing to nap completely even when I wanted to take a nap in the middle of the day I just couldn’t. My emotions are controlled now. Anxiety and depression are kept at bay. Sometimes I get lazy and stop taking them and about a week later I start feeling all my old symptoms again. Currently I take trinity, spice and ACB. I have not gotten sick this whole winter season even though I’ve been around multiple people with colds and the flu. What I found extremely weird though is that normally I get crazy horrible miserable cedar allergies dec-March and usually I have to take Allegra EVERY SINGLE DAY during these months. I have only had to take Allegra a handful of times during these past months. It’s so bizarre because I’ve always struggled with severe cedar allergies my whole life except for this past season!
My mom has always had high blood pressure but recently it got bad enough that the doctor put her on meds. She didn’t like the side effects so I told her about how I thought the peel blend might help her. A few days into taking the peel her blood pressure was normal, she says she feels great and has more energy. My dad has even noticed a difference in her mood and will ask her if she’s taken her peel if she’s acting cranky. She’s about to be on her third bag of peel!
Thank you so much Gavin. I look forward to trying out Apigenin and Nebula next.
Rated 5 out of 5
Roberta Jackson (verified owner) – April 9, 2019
I am 60 yrs old and I have had a lifetime of trying to lose weight and be healthy. I was Vegetarian from 18 yrs. old and for many, many years. I became grain free, practiced intermittent fasting and and water fasting for the past 10 yrs. and although my blood results have always been good for being overweight, I still was unable to lose any significant weight.
My Mother came to live with us 10 yrs ago at the age of 89 with the life expectancy of 2 yrs. She had been formally diagnosed with Alzheimer’s. In the first 6 mths. that she lived with me, I weaned her from her drugs and she went on to the same way of eating as my family. My Mother is now 98 1/2 yrs old. She has lived 10 years beyond what the Dr. said she would live. Still with dementia but, never had anything more than a slight cold in 10 years.
In the winter of 2018, I first started hearing about dry fasting. I had done two 30+ day water fast in my life and many juice and water fast but, had never heard of dry fasting before.
At the end of Jan. 2019 I did my first 44/4 dry fast. Loved it! I found it easy to do and I lost 14 lbs. on the first cycle. I continued on with more cycles of dry fasting and then on March 10th. my Mother unfortunately had aspiration pneumonia and ended up in the hospital for four days. I took her out because they or of course were taking us down a road of death purely because of her age.
I brought her home and she started doing very well the next day. While, I was at the hospital with her I Messaged Gavin to ask him a couple of questions about my dry fasting experiences, at this point I was not using the blends. Gavin being the extremely Special & generous person that he is, offered to send me some samples of his blends. They could not have come at a better time! Because I chose to bring my Mother home early, I ended up having to do a lot of her life-saving needs that kept me up a few nights and my days became extremely busy with having visits from nurses, bathers, Social workers etc. I was on the blends at this point and even though I was going through a very trying time trying to help my Mother survive, I chose to continue on with my dry fasting cycles. I have read from other people about having so much more energy on the blends but, unfortunately where I didn’t feel an abundance of energy, I think they were saving me from becoming the next hospital victim. I have heard all the stories about Caretakers and how they would die even before the person they were caring for. I promised myself when we took in my Mom that I would not let that happened to me. I have too much to live for.
“Trinity” seemed to keep me even keeled and capable of handling all the stress that I was bombarded with. It helped me sleep very peacefully at night and ready to take on the next day. “Matcha” definitely gave me energy enough to get through another trying day. I have done 14 dry fasts since Jan and I have lost 44 lbs. Losing the weight obviously helped me to care for my Mom as well.
“Peel” has also helped to improve how I feel while dry fasting. My nails are growing quickly and my skin is looking healthier instead of tired.
I know for sure if it weren’t for the blends I never would of been able to keep up the stamina of caring for my Mom, Husband, Grandchildren or myself.
I’m so grateful for the Dry Fasting group board and all the advice and support. I am inspired by all the others who are successfully becoming their true selves. But, most of all so blessed to have come across Gavin and all of his wonderful gifts of knowledge and wisdom that he is so graciously sharing with the world.
I am also glad to be putting my Husband’s health and mine back together, instead of falling apart. We will definitely continue to use Interstellar blends to help mend and repairing ourselves for happier & healthier Senior years to come. Thank you Gavin!!!!
Rated 5 out of 5
Rich Ryan – August 21, 2019
“Wanted to share that I’ve experienced a significant decrease in my heart disease symptoms over the last year since I doubled my Spice/Peel intake. I can tell the main blockage on my Widow Maker artery on the back of my heart, that I’ve been carrying for over 15 years, has shrunk significantly. The proof is that when I have a bad day and eat all kinds of crap that I shouldn’t eat, I experience almost no symptoms from it. A year ago I would’ve almost died from eating all that garbage. Now, almost nothing.
Also, my depression is pretty much gone since starting Apigenin, Luteolin, and supplementing with Mag, Zinc and Lithium. 1/4 tsp API, 1/2 tsp Lut, 4 caps Mag and Zinc, 10 drops Lithium. Twice a day for all.
My Spice/Peel intake is 2 tsp 20:1, 1/2 tsp 200:1. I alternate between 20:1 and 200:1. Usually do one of them 20:1 and the other 200:1, and switch it up every month or two. Take one in the morning, the other in the evening.
So Gavin has hit on the cure for arterial blockages as well. Amazing stuff!”
Rated 5 out of 5
Julia Bienkowski – September 3, 2019
Thank you Gavin! I have struggled with psoriasis for 20 years and have tried every product on the market. Within the first week of taking Peel, my skin became noticeably clearer. By the second week, my entire body is completely clear! The fine lines around my eyes are gone, my hair and nails are growing stronger and thicker and I feel fantastic! Another amazing product to add to my Interstellar regimen. Smiling from head to toe!!
Rated 5 out of 5
Michael James – October 27, 2019
First off, Id like to show my appreciation for Gavin and all of the hard work he does to run this operation and provide us a way out from the traditional health system! At first, I was very hesitant and skeptical about the potential of the interstellar herbs and all the positive claims. After doing some research, I realized that all the modes of healing that his approach consists of, comes from years/months of his personal study. The advice he gives helps us restore our body and reclaim our optimal performance. If you follow his protocol without deviating from it, you will achieve your health goals. The problem is that people try to add in their two cents and end up swaying from the result proven regiment!
After studying the website for while, I decided to try the herbs out. I ordered Trinity, Spice, Peel. Within 1.5 weeks of consistent intermittent dry fasting, keto/paleo diet, my inflammation decreased, yellowing of the skin subsided, eyes began to whiten, sleep began to feel as I was a child again, and mood levels/emotions started to balance. I forgot what it felt like to be foggy, groggy and unhealthy.
If you are contemplating trying these out, really sit down and prioritize what health means to you. Do the math, people see the price tag and immediately turn away. How much are you spending eating out? How much are you spending on your daily Starbucks? How much are you spending on junk that you don’t need? Now do some calculations on a couple months of herb supply! Sit down and ask yourself, how much does living a healthy, enhanced, balanced quality of life mean to you? Weight out the pros and cons between your stupid spending and living healthy. Don’t be stupid!
Rated 5 out of 5
Bri Ryma – March 3, 2020
I truly wish I could give this blend a higher rating than 5 stars. If I would have know how impactful this blend would be, I would never have waited to purchase!
A little back story. I have PCOS, that has caused 10 years of infertility, and extreme insulin resistance. Because of the insulin resistance, controlling my blood sugar has been a huge struggle. I was waking up every morning so puffy and lethargic. Mid way through the day I would crash with mood swings and exhaustion. Night time would come, and I was up with crazy insomnia. It was a vicious cycle. I never felt good unless I was fasting. Even eating a ketogenic diet wasn’t helping.
With in the first 24 hours of taking peel I started feeling better. For the first time in a long time I woke up and wasn’t puffy and miserable! Then came time for my normal mid day crash, and it didn’t happen!! I have now been sleeping great, and overall feeling better and better each day. I understand the science behind this product, and it truly amazes me that everyone isn’t running to buy this. With PCOS being the new epidemic effecting 1 in 10 women, this could be key to helping reduce insulin resistance and start to heal their bodies! Thank you Gavin for putting in the work to change lives!
Rated 5 out of 5
Allie Tyre (verified owner) – March 8, 2020
First, I am a relatively new user of these blends. And as I add them, I keep just getting more and more amazed. I love all I have used, but Peel is just special.
I had been battling planters fasciatis for about 6 months. For those of you who don’t know what that is, it is basically a connective tissue disorder (i.e. extreme inflammation!!!) around the arch/heel conjunction of your foot that can cause excruciating pain. Nothing i did helped it and “resting it for 6 weeks” was not an option. I decided to try Peel for this.
I began megadosing it right after I arrived, like 1 teaspoon 3 times a day. One day, about 7-8 days later, I was up and about, doing my normal morning routine when it suddenly occurred to me: my foot was not hurting. Not even one little bit. Of course, my skepticism immediately kicked in. So, what did I do? Go on a 3 mile walk. Yup. Next day–no pain. Day after that– no pain. And not a single day of pain since. I’ve since reduced my dose of this glorious blend, but i will take it until the day they pry it out of my cold, dead hands! Thanks, Gavin!
Rated 5 out of 5
Natalie Leal (verified owner) – April 2, 2020
I was recently made aware of this company and the amazing powerful powers of the Interstellar blends by means a great friend. My first order included the Peel which I have been taking for close to 2 months now. I can see how my skin has been going through a sort of metamorphosis as my system has been cleaning house and clearing things out of my body! This makes sense when our skin is one of our most major organs! I’m excited to add a few more blends to my list and continue to see the changes and healing affects these blends bring out.
Thank you so much for making these available and with all the research that is involved and progress moving forward with new products . I can’t wait to continue my journey with these amazing blends!
Rated 5 out of 5
Lisa M Sherrill (verified owner) – April 14, 2020
I have been taking PEEL and Pine Pollen for 3 weeks now. I noticed a different in energy and alertness, 20 minutes after the first dose. My eyes opened, my shoulders straightened and my body took a sigh of relief. I wondered if I had taken a drug or an herb, as the shift was so noticeable. Since then, I have noticed that I am not as tired during the day. I keep moving and it surprises me, as I am use to having to sit a lot to recover after exercise.
Along side this, I have scar tissue buildup / adhesions on my right hip that prevents me from gaining full range of motion. Crossing my right leg over my left has been impossible for a couple of years now without incredible pain. I have some how gained about 2 – 3 inches more range of motion in last couple of weeks and less pain. I haven’t been in bed, wincing in pain. I’m not sure which of the two herbs could have helped with this?
Lastly, I will be continuing to take PEEL for a long time to come, and will not go elsewhere to find a more solid flavonoid. I can tell my body has taken to this more than other brands I have tried in the past. My body feels the difference in quality.
Rated 5 out of 5
Heather Barrington – April 22, 2020
I absolutely LOVE this blend. I’ve had thyroid issues as long as I can remember and my symptoms are leaving one by one the longer I take this. Thank god for these.
Rated 5 out of 5
Antonio (verified owner) – July 23, 2020
After taking PEEL combined with SPICE for 90 days now, I feel like I’ve never felt before, I feel GREAT and my skin GLOWS. (LITERALLY) I am usually not one to leave reviews on products but out of gratitude I feel I have to leave this one. I used to be one to catch a cold all year round. In Winter months I’d be sick half the time and during the summer due to getting in and out of A/C in the car, the slightest temperature would trigger a cold in me. I hate getting because when I do I get the whole package of body aches, stuffed nose and chills but it’s been about 3 months and I have not gotten sick. It’s WEIRD. NOT EVEN A SNIFFLE. I have never felt like this since as far as I can remember. I have not gotten sick ever since taken this, not even a sniffle. I feel strong and my acne has cleared up. It almost as if this stuff regenerates you. I just want to thank Gavin for creating such products and now I just feel like buying a bunch and hoarding it for the future. Thanks man.
Rated 5 out of 5
Joanie Morgan – July 31, 2020
I can’t live without my Peel. I am compelled to write this review because of what this AMAZING herb did for my dog. So my dog hasn’t been feeling well for over 3 weeks now. I’ve been taking him to the vet and with a bunch of money wasted, my poor Kilo just wasn’t himself with no energy and would barely eat. The past 2 days I’ve been mega dosing him with Peel. After the first day, I felt like he was coming back to life. After the 2nd day, he was back to his normal self and back to eating and running around with tons of energy. Why the heck didn’t I think of doing this before wasting so much. You guys, Peel is my go to for anything with my family. If I hear a cough or a sniffle from anyone in my family, I’m forcing them to take a mega dose of Peel. I can’t say enough about this blend. Gavin has the magic y’all. Just dive right in and get you some of this here Peel. Well not just Peel but everything that he has. I can’t thank you enough Gavin. You have been a life safer for myself and my whole family. Mahalo nui loa
Rated 5 out of 5
jet – September 8, 2020
All i gotta say is WOW! I do realize this is only the beginning of the benefits ,but after only taking this stuff for a few days my eczema on my arms and legs is already about 85% clear. Gavin also graciously decided to put in trinity as a sample ( which i was very excited about ) i heard about Gavin through a trader by the name of Shaun lee, who i’ve been seeing post about these herbs time and time again. i was hesitant to get them, but really curious to see if they would work and i ended up being gifted peel for my birthday from my brother. But after taking trinity for only a few days twice a day, one in morning and once at night. I have noticed a HUGGEE difference in my trading psychology. I payed very close attention to my emotions on this stuff and i can honestly say this is the real deal. no BS. Its truly amazing what these blends can do. No fear, No hesitation just cool calm and collected. i’m very excited to stock up on more and see more of what Gavin has to offer.
Rated 5 out of 5
Dana Beaurem (verified owner) – November 28, 2020
PEEL and SPICE!!! I can go on and on about this combination of blends. My skin has never looked better (the glow is real) and felt smoother (soft) in the winter months. I’ve always had dry skin but the Peel and Spice combination has given we a glow that is amazing. People keep asking what i use on my skin and when I tell them and show them they don’t want to purchase because they want to stick with the store bought sh*%. But for me it’s the PEEL and SPICE that I KNOW is the reason.
Rated 5 out of 5
~Odz – March 29, 2021
Apologies for the delayed review, I wanted to try the blends for a few weeks so I could leave a genuine opinion!
Firstly I want to mention how quick these blends arrive wherever you are in the world, package came within 3 days to the UK from USA, crazy!! No messing around Gavin! I was able to start my fast a lot sooner than anticipated…
The blends themselves are life changing if you stick to protocol with the science backed FACTS! My life has changed drastically these past 3 weeks and the blends have made fasting a lot more easier and enjoyable! I totally recommend to even start off with one then work you way up (challenge combo is great)
My face has cleared up completely and I feel and look better all around, blends, coffee and fasting with 22/2 is now my new lifestyle and I wouldn’t change it for anyone! thanks again Gavin and team.
Rated 5 out of 5
Misba (verified owner) – April 22, 2021
Before trying these blends, I was very sceptical as to whether or not they would work. However after trying them, I am absolutely mind blown by the effects!
Initially I was introduced to the blends by Shaun Lee. Being a trader myself, I was seeking anything which could give me an edge or help me even be that 1% better with trading. Initially I was only looking to order Trinity however after joining the telegram group and having a conversation with Gavin, I realised that there were also blends which could help with my eczema. Having suffered with eczema all my life and always being prescribed with steroid creams (which only work temporarily) I was keen to try Peel and Spice on Gavins recommendation and see whether or not that made a difference.
The results were remarkable! After a couple of weeks, I was able to consume foods which would normally cause a reaction to my eczema, however by taking the blends everyday, there seemed to be no eczema flare up. Not only that, my skin was visibly getting clearer every week. These blends have made a massive difference In my life and I am forever grateful! Then we have Trinity which is in its own league! The mindset clarity and focus was incredible and unlike anything I have experienced before. This has helped tackle one of the most important aspects of trading, psychology and emotions. I am about to do a big re-stock on these blends and recommend anyone who is on the fence with them to take the leap of faith and order them! Thank you Gavin for what you do, you are changing lives!
Rated 5 out of 5
Courtney – August 22, 2021
I am just getting over covid (didn’t get tested but had all the classic symptoms). The first week was lots of ups and downs with body aches, but not too bad. In the second week it got a lot more intense, with persistent lung and sinus inflammation that made it very hard to breathe. This would spike my adrenaline and I was barely able to sleep for several days in a row, which wreaked havoc on me physically and emotionally. On day 9 of the sickness I got in touch with Gavin, and he suggested megadosing Peel and Spice (3-6 tsp daily), and taking Luteolin, Victorious (the anti-viral blend) and Senolytic. I started doing all this, as well as eating as low glycemic as possible with my weird appetite at the time, and started feeling some inflammation relief within a couple of days. I kept up on the herbs and slowly improved over the next week, unwinding my body from the intense stress and inflammation state it had been in. I am not usually strongly affected by viruses,and am usually only sick 2-3 days, if at all. This one was much longer and more intense. I am happy to say I feel almost completely recovered now, and I know the herbs helped a ton!!
Rated 5 out of 5
Paul (verified owner) – October 11, 2021
So every year I go and get wood for the winter. Where I live, it makes the most sense to burn wood for heat, plus it’s enjoyable. Usually.
Just yesterday, I was loading the wood into my trailer, tossed one of the big logs up on the stack, and my left shoulder popped three times. It hurt for a minute, but then got back to normal mostly, but with the promise of a debt of pain. Like the stubborn cuss I am, I kept loading wood and tossing it. And just like my shoulder promised, I could barely move it come bedtime. In fact, it hurt so bad it kept me up most of the night.
If I take Peel at night, I stay awake, so I suffered through it and then come morning–you better believe the first thing I did was make me up a cup of hot cocoa (not the alkalized, fake crap, but the good stuff) with half a teaspoon of 20:1 Peel (and Spice too, because mixing the two packs one helluva punch).
Within about twenty minutes, the pain and tightness in my shoulder fell away, and I had full mobility again. I love this stuff!
How I typically use Peel is for muscle recovery. After a hard workout (or in this case being dumb and stubborn), I load up on the Peel and it helps the soreness go away faster than just about anything else I’ve tried.
A couple months ago, I was on a trip with my wife, bent over and had a muscle spasm in my back. Felt like a geezer; I could barely move (for some reason, every so often I get muscle spasms in my low back; started after my first surgery when I was 19). Ibuprofen didn’t touch it, and I didn’t have access to any Peel for the day.
But when we got home half a day later, I did a massive dose (1 teaspoon Peel 1 teaspoon Spice) and the pain lessened. Next day, I did the same and kept up the high does for three days, and within that time, all of the terrible spasms went away. I lowered the dose for a few days, but kept it higher than normal, just to allow for more healing, and it worked beautifully. From what I’ve seen, typical treatment for this type of spasm is pretty strong muscle relaxants plus opiates depending on the doctor for ten days to two weeks. That doesn’t sound like a good option to me, considering all of the side effects.
So I kept with the Peel and in way less time, less money, and less pain, I was good as new.
I love this stuff.
One last story.
My daughter broke her arm on our trampoline this last year. It was a terrible fracture where the radius snapped in half, and not clean, plus another fracture in her ulna, and a dislocation in her elbow. The Orthopedic Surgeon was able to somehow set the bones without surgery, which was a small miracle, but it was going to be a long road to recovery.
I asked Gavin how much Spice and Peel to give her and he recommended 1tbs of each, once or twice a day until the bones healed. When it came time for more X-rays the doctor was legit surprised at how well her arm had healed and that surprise continued with each recheck until we were finished seeing him.
Highly recommended.
Rated 5 out of 5
Jamie – October 27, 2022
Firstly, I’d like to thank Gavin creating so many amazing products that truly make a difference to our lives, for the better. Since and prior to placing my first order in 2020, Gavin has always been willing to offer his advice and give his time freely when discussing health and wellbeing, with geniune intentions – something which is rare in the world we live in today.
These blends do perform miracles, but they are not just for those who are sick. I had a clean bill of health and felt good physically and mentally when purchasing my blends, with the intention of taking my wellbeing to another level – and that it did! My clarity and focus skyrocketed from a place where I was already performing very high mentally. Motivation was through the roof, friendships improved, relationships improved, fitness improved, energy… X10! I was optimising every area of my life through these blended herbs and fasting. Fast forward to today, 2 years on, and I can assure you that there is no better product out there on the market (or not even on the market) that can achieve the things these blends do!
The first batch of blends I ordered that changed my life were Trinity, Peel & Spice, plus Supernova. Gavin is always perfecting his craft and curating new blends through VERY in-depth research. I have the utmost confidence when purchasing and trying the new blends he puts together and will continue to do so for life.
***** Customer Service
***** Shipping
***** Product Quality
Rated 5 out of 5
Luis chavez (verified owner) – November 29, 2022
Well where can I even start? I sat on the side lines for many years just observing Interstellar Blends by recommendation of Shaun Lee. I watched Gavin’s movement before I ever considered pulling the trigger. It wasn’t until I saw that he had remedies for psoriasis which is what I have been suffering from for a few years now so I figured hey this is my chance! I pulled the trigger and it has been the best decision I have ever made!! No regrets whatsoever
To begin I started off with stomach reset combo and let me just say it has been a game changer for me. In just the short amount of time of me trying it out I saw more positive results in a week than any cleanse/ diet I have been on the last couple years. The alleviation my stomach felt was next to none and don’t even get me started on that PURGE!! Feel the burn baby it takes a lot of mental strength for these powerful blends but in time you too will feel invincible using them. What’s quite amazing is that months after the stomach reset you still feel the effects and how much it has changed your body. Foods that used to be really hard to digest for me became a thing of ease. It was almost like I hopped into a whole new body.
After this amazing cleanse I tapped into all the other blends and I just have to say I CANNOT just choose one they’re all so exquisite in their own ways. From someone that has dealt with addictive personality issues these blends have completely transformed my way of being I am much more calm and collective now. I do have to give a standing ovation to a few particular blends however those would be SPICE-PEEL-TRINITY-REWIRE- VICTORIOUS
These blends have absolutely transformed me as a human being and have made my relationship with my psoriasis condition so much better. It hasn’t gone away completely but these blends fight and they fight hard!! They have managed to give me more progress than anything any hospital or clinic could possibly offer me. The amount of relief and satisfaction I get out of life makes these blends so worth it. Whether you’re dealing with any mental issues or physical or you simply want to live better. INTERSTELLAR BLENDS is the ultimate championship elixir of life just scoop some of those magical blends into a perfectly brewed cup of coffee and enjoy the ride! I feel absolutely proud to be part of this movement of fasting and achieving optimal health because at one point I just wanted to give up.. now that I know about these blends my life has forever changed. Thank you Gavin for all your hard work 💯 BAAAMMM!!!
There is so much more to be said about each individual blend but that would take an entire book to write! In a few words I’d describe the blends as
LIFE SHAPING
SACRED
HOLY
POWERFUL
WORLD CLASS
ALLEVIATING
POWERFUL
Rated 5 out of 5
Luis E Garcia (verified owner) – March 8, 2023
AT LAST–A PRODUCT THAT FINALLY DOES WHAT IT SAYS!!
In short, I’ve been diabetic for over 20 years–unfortunately, I neglected taking care of myself while taking on the world. In addition, I have diabetes types 1& 2 running on both sides of my family.
Always having been interested in optimal health, I changed my diet years ago, becoming vegetarian and eventually vegan. I tried many supplements and “breakthrough miracle cures” along the way, but always the same result–although my diabetes seemed to improve some, the ever-present dangers were still there–the threats of blindness, neuropathy, kidney failures, etc…
Doctor prescribed medications did little to nothing to help, and only seemed to disagree with my body as time went on–often making matters worse! That doesn’t even include the worries of having my liver, kidneys and other organs affected later on as a serious side effect.
It seemed that, contrary to my hopes, I was only prolonging the inevitable failure of being overtaken by this disease, despite my own extensive research and learning, and my arduous attempts at striving for excellent health!
Finally, my daughter, who shares my interests, turned me on to Interstellar Blends. Despite many testimonials, I studied some of the extensive research provided and decided to give it a shot, hoping to find the one product that would at least make a difference…and IT ACTUALLY WORKED!! FROM DAY ONE!! It began lowering my blood sugars after meals significantly, and much quicker than my fast-acting insulin–even preventing those overnight spikes I dreaded! Till this day, this PEEL blend has truly provided the remedy to my disease and my fears–in less than 3 months now–making me virtually insulin-free after 20+ years! ONE IMPORTANT NOTE: You MUST take the blends as recommended, at least until your absolutely sure that you can lighten up on the dosage! I made that mistake, thinking that I had been miraculously permanently cured after two weeks of GREAT results–lesson learned!
PROOF THAT THERE IS A CURE FOR VIRTUALLY ANY ILL IF WE CHOSE TO CARE AND SEEK FOR IT! I vouch for no other product to fully do what this product sets out to do. Definitely worth every penny!
Thank you, Interstellar team for the renewed hope!

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