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Jayaraman, S. Plant Sterols in Diabetes Management. Encyclopedia. Available online: https://encyclopedia.pub/entry/16871 (accessed on 16 November 2024).
Jayaraman S. Plant Sterols in Diabetes Management. Encyclopedia. Available at: https://encyclopedia.pub/entry/16871. Accessed November 16, 2024.
Jayaraman, Selvaraj. "Plant Sterols in Diabetes Management" Encyclopedia, https://encyclopedia.pub/entry/16871 (accessed November 16, 2024).
Jayaraman, S. (2021, December 08). Plant Sterols in Diabetes Management. In Encyclopedia. https://encyclopedia.pub/entry/16871
Jayaraman, Selvaraj. "Plant Sterols in Diabetes Management." Encyclopedia. Web. 08 December, 2021.
Plant Sterols in Diabetes Management
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This entry is adapted from the peer-reviewed paper 10.3390/antiox10121903

The plant-based food we consume often contains many sterol-based bioactive compounds. It is well documented that these compounds could effectively manage the processes of insulin metabolism and cholesterol regulation. Insulin resistance followed by hyperglycemia often results in oxidative stress level enhancement and increased reactive oxygen species production. At the molecular level, these changes induce apoptosis in pancreatic cells and hence lead to insulin insufficiency. Studies have proved that plant sterols can lower inflammatory and oxidative stress damage connected with DNA repair mechanisms. The effective forms of phyto compounds are polyphenols, terpenoids, and thiols abundant in vegetables, fruits, nuts, and seeds. The available conventional drug-based therapies for the prevention and management of diabetes are time-consuming, costly, and with life-threatening side effects. Thereby, the therapeutic management of diabetes with plant sterols available in our daily diet is highly welcome as there are no side effects. 

diabetes insulin resistance plant sterols enriched foods

1. Introduction

Diabetes mellitus (DM), commonly known as diabetes, is an endocrine disorder characterized by elevated glucose levels [1]. The pancreatic cells produce a metabolic peptide hormone called insulin which allows the entry of glucose from the blood to the cells to support them with energy. A lack of adequate insulin functional balance plays a vital role in diabetes development [2]. Diabetes is a chronic disease, and its global prevalence is estimated to be 4.4% in 2030. According to the International Diabetes Federation (IDF) data, it is estimated that by the year 2045, about 693 million people will be affected by diabetes worldwide, and the most badly hit countries will be the USA, China, and India [3]. Diet plays a significant role in the etiology of many diseases such as diabetes, cancer, and cardiovascular illness, even at a younger age. A healthy diet pattern (less salt, sugars, saturated, and industrial trans-fat but with more green and leafy vegetables and fruits) is essential to maintain good health and to prevent many diseases. Having the habit of following an unhealthy and uncontrolled diet is considered one of the fundamental reasons behind the induction of obesity and overweight [4]. The overweight and obese conditions can lead to many unhealthy situations such as cardiovascular diseases, muscular-skeletal disorders, and certain cancers associated with breast, ovarian, colon, and liver. At present, the epidemic death proportion due to obesity-related diseases has reached at least 2.8 million deaths per year globally [5].
Abnormal accumulation of fats results in insulin resistance, impaired glucose tolerance, and even diabetes [6]. In obese conditions, the level of major inflammatory proteins such as interleukin-6 (IL-6) and tumor necrosis factor (TNF-α) increases significantly. Elevated levels of these inflammatory markers induce dyslipidemia by inviting macrophages towards the adipose tissue [6][7]. Various conditions such as programmed cell death in pancreatic β cells due to insulin resistance, hyperglycemia-induced oxidative stress, and enhanced production of reactive oxygen species can lead to diabetes. The phytosterols are natural compounds that include sterol and stanol esters and are abundantly occur in plants’ cell membranes. The plant sterols that are commonly present in daily food intake are the β-sitosterol, campesterol, and stigmasterol. Due to the structural similarity with the body’s cholesterol, the phytosterols compete with the cholesterol and help in reducing the absorption of dietary cholesterol [8]. The European Foods Safety Authority (EFSA) declared that the daily consumption of plant sterols within the therapeutic dose (1.5–2.4 g/day) is adequate for disease prevention in humans without harmful side effects [9].

2. Plant Sterols and Anti-Cholesterol Activity

The human body requires the waxy substance cholesterol to build healthy cells and synthesize hormones and digestive fluids. Overall, cholesterol within the required range helps our body to function correctly. An imbalance between the two forms of cholesterol, such as low and high lipoproteins, increases the chances of developing heart disease and stroke. The hypocholesterolemic effect of plant sterols was identified in early 1950 [10]. Still, many studies are in line to identify the molecular mechanism behind the anti-cholesterol effect of PS. So far, many studies emphasize that the plant sterol could regulate the levels of lipid variables such as LDL, HDL, triglycerides, and apolipoprotein B effectively [11]., Many studies have supported the lipid regulatory action of plant sterols; however, a lack of understanding of the mechanism prevents them from being used in clinical trials. Many reports have suggested that the plant sterols and stanols could reduce LDL levels and exert their action in a dose-dependent way [12][13]. Some data also show that the stanols could exert a dose-dependent hypocholesterolemic effect compared to sterols [14]. The efficiency of plant sterol may largely depend on the baseline levels of plasma lipids. Studies have shown that plant sterols could effectively lower the concentration of triacylglycerols and thereby reduce the synthesis of very-low-density lipoproteins. Conversely, a few detailed research studies have highlighted the negative association of phyto compounds with hypercholesterolemia impact [15][16].

3. Plant Sterols and Anti-Diabetic Effects

Plant-based medicines are commonly used to prevent many chronic diseases. They have been in use as a complementary or alternative therapy form since ancient times. For example, the anti-diabetic drug metformin, a derivative from the plant Galega officinalis, is widely used to prevent diabetes [17][18]. The other medicinal plants with anti-diabetic properties include Aloe vera, Jamun/Indian blackberry, gurmar, bitter guard, basil, yacon, fenugreek, etc. The various parts of the plants, such as leaves, seeds, roots, and fruits are used to treat diabetes [19][20][21][22][23][24]. These medicinal plants regulate many functions such as insulin secretion, insulin resistance, glucose absorption, and regulation (Table 1).
Results from animal studies have supported the potent hypoglycemic and hypocholesterolemic effects of plant sterols [25][26][27][28]. However, so far, no clinical research has been conducted to verify the impact of plant products as conventional drugs for diabetic management. The plant sterols could regulate the expression of genes such as glucose-6-phosphatase, phosphoenolpyruvate carboxykinase, and peroxisome proliferator-activated receptor-alpha and influence the rate of metabolism [29]. Misawa et al. reported that the ethanolic extract of Aloe vera could increase the production of insulin in Zucker diabetic fatty rats [30]. Research by Patil et al. proved the insulin-secreting efficiency of plant sterols present in cumin oil, cumin aldehyde, and cuminol with the help of the diabetic rat model [31]. The research identified that the plant sterol present in black cumin (N. sativa) blocks the sodium-dependent passage of glucose across the jejunum. Long-term treatment of N. sativa modulates glucose tolerance and body-weight reduction as equivalent to metformin in a rat model [32]. Indian satinwood (Chloroxylon swietenia) shows a significant hypoglycemic effect in streptozotocin-induced diabetic rats [33]. The ethyl acetate extract of fruits of weeping forsythia could effectively enhance the plasma level of insulin [34]. The ethanolic extract of scarlet gourds (Coccinia grandis) leaves exerts its hypoglycemic activity by reducing the plasma glucose level and increasing the serum insulin level [35]. These plant compounds are noticed for their ability to induce hypoglycemic impact via improving the mechanism of insulin secretion.
Research using the common nettle (Urtica dioica) leaves extract identified the gender-biased working modulation of plant sterols. The study proved that the compound could balance hypoglycemic activities in male Wistar rats. It could effectively reduce the plasma glucose level and fasting insulin resistance index in male rats [36]. The extract of cashew tree (Anacardium occidentale) could significantly reduce the blood glucose levels in STZ induced diabetic rats. In this experiment, the compound showed its ability to reduce fasting glucose levels [37]. An oil extracted from garlic (Allium sativum) helps to improve insulin secretion and glucose tolerance. It proved that the extract could enhance glycogenesis by increasing GLUT4 expression in the rat model [38]. The bark extract of the Sapphire berry family (Symplcos cochinchinesis) has been shown to improve insulin resistance and thus reduce glucose levels [39]. Similar results are observed upon the use of the extract of Helicteres angustifolia [40]. Other plant extracts that work by a similar mechanism to reduce the blood glucose level with effective insulin sensitivity modulation include the Pleurotus ostreatus, Afzelia africana, Uvaria chamae, and resveratrol [41][42][43][44].
Some phyto compounds act by inhibiting the α-glucosidase, thereby preventing carbohydrate metabolism. Reduced carbohydrate metabolism results in a decreased rate of glucose assimilation and could lead to a reduced postprandial glucose level in the blood. Many plants such as basil contain phyto compounds that inhibit enzymes such as α- glucosidase and α-amylase, thereby acting as a potent anti-hyperglycemic agent [45]. On chromatographic separation, the basil leaves are found to contain flavonoids, glycosides, steroids, and tannins [46]. The polyphenol compounds isolated from the jute plant exert its potential by inhibiting ACE and lowering the levels of α- glucosidase and α- amylase significantly [47][48]. Certain legumes like soybean have been shown to contain polyphenolic compounds such as isoflavones [49]. The phyto compounds of fig fruits such as vitexin and isovitexin were shown to have glucose reduction properties in sucrose-loaded mice [50]. The figs (Ficus deltoidea) are considered an alternative natural remedy for diabetes and are also available in many commercial forms. Plant sterols have been shown to improve insulin production, GLUT4 expression, and insulin sensitivity. As well it inhibits α glucosidase, α amylase, and ACE functions. In addition, the plant-derived compounds also regulate genetic and epigenetic factors to counteract diabetes. More clinical research is necessary to support the therapeutic potential of plant sterols in preventing diabetes.
Table 1. Anti-diabetic activity of different herbs.
Botanical Name Common Name Components Used Animal Studies Effects Reference
Aloe barbadensis Aloe vera Leaves Diabetic rats Significant reduction in the levels of the enzymes that facilitate carbohydrate metabolism [30]
Cuminum cyminum Cumin seeds Diabetic rats Improves insulin secretion [31]
Nigella sativum Black cumin Seeds Rats Improves glucose tolerance [32]
Chloroxylon switenia Indian satinwood Barks Diabetic albino rats Decreases blood glucose level [33]
Forsythia suspense Weeping forsythia Fruits STZ induced Kunming mice Significant reduction in blood glucose level [34]
Coccinia grandis Scarlet gourds Leaf Diabetic Wistar rats Improves insulin-secretagogue and cytoprotective activities [35]
Afzelia africana African mahogany Stem Diabetic Wistar rats Reduces hyperglycemia [42]
Urtica dioica Common nettle Leaf Fructose induced Insulin resistance Wistar rats Significantly reduces hyperglycemia and insulin resistance [36]
Anacardium accidentale Cashew tree Leaf Diabetes induced female albino Wistar rats Significant reduction in the levels of serum glucose, glycosylated haemoglobin, FIRI, and serum insulin [37]
Pleurotus ostreatus Oyster mushroom   Diabetes induced male Wistar rats Significant reduction in blood glucose level [41]
Uvaria chamae Bush banana Root Diabetes induced albino rats Significant improvement in the regeneration of islets of Langerhans [43]
Cinnamomum zeylanicum Cinnamon Bark STZ-induced rats Significantly diminishes α-glucosidase activity [22]
Ocimum basilicum Basil Leaves   Significantly inhibits α amylase activity in a dose-dependent manner [46]
Corchorus olitorius Jute Leaves   Significantly inhibits the enzymatic activities of α-amylase, α-glucosidase, and ACE [48]
Ficus deltoidea Fig Leaves, Flowers STZ-induced diabetic rats Significantly lowers the blood glucose level [50]
Holarrhena antidysenterica Bitter oleander Seeds Starch-loaded normoglycemic rats Interferes with starch digestion [24]
Olea europaea Olive Leaves STZ-induced diabetic rats Inhibits α amylase activity [21][23]
Glycine max Soybean Soybean   Significantly lowers the levels of α-amylase, α- glucosidase and ACE [49]

4. Conclusions

Phyto compounds, the naturally obtained formulations from plants, are well known for their effective anti-diabetic properties. They can exert their function directly by interacting with several signaling pathways associated with diabetes. They also have a potent hypocholesterolemic effect, which could indirectly counteract those obesity-related issues connected with diabetes. In conclusion, we strongly support that due to fewer side effects with significant medicinal character, plant sterols and stanols can be widely used to prevent diabetes. More clinical trials are needed to reveal the anti-diabetic benefits of plant compounds to commercialize them as therapeutic agents.

References

  1. American Diabetes Association: Diagnosis and classification of diabetes mellitus. Diabetes Care 2009, 32, S62–S67.
  2. Röder, P.V.; Wu, B.; Liu, Y.; Han, W. Pancreatic regulation of glucose homeostasis. Exp. Mol. Med. 2016, 48, e219.
  3. Cho, N.H.; Shaw, J.E.; Karuranga, S.; Huang, Y.; da Rocha Fernandes, J.D.; Ohlrogge, A.W.; Malanda, B. IDF Diabetes Atlas: Global estimates of diabetes prevalence for 2017 and projections for 2045. Diabetes Res. Clin. Pract. 2018, 138, 271–281.
  4. Purnell, J.Q. Definitions, Classification, and Epidemiology of Obesity. In Endotext; Feingold, K.R., Anawalt, B., Boyce, A., Chrousos, G., de Herder, W.W., Dhatariya, K., Dungan, K., Hershman, J.M., Hofland, J., Kalra, S., Kaltsas, G., et al., Eds.; MDText.com, Inc.: South Dartmouth, MA, USA, 2018.
  5. Ahirwar, R.; Mondal, P.R. Prevalence of obesity in India: A systematic review. Diabetes Metab. Syndr. 2019, 13, 318–321.
  6. Gutierrez, D.A.; Puglisi, M.J.; Hasty, A.H. Impact of increased adipose tissue mass on inflammation: Insulin resistance, and dyslipidemia. Curr. Diabetes Rep. 2009, 9, 26–32.
  7. Leitner, D.R.; Frühbeck, G.; Yumuk, V.; Schindler, K.; Micic, D.; Woodward, E.; Toplak, H. Obesity and Type 2 Diabetes: Two Diseases with a Need for Combined Treatment Strategies—EASO Can Lead the Way. Obes. Facts 2017, 10, 483–492.
  8. Cabral, C.E.; Klein, M. Phytosterols in the Treatment of Hypercholesterolemia and Prevention of Cardiovascular Diseases. Arq. Bras. Cardiol. 2017, 109, 475–482.
  9. Martianto, D.; Bararah, A.; Andarwulan, N.; Średnicka-Tober, D. Cross-Sectional Study of Plant Sterols Intake as a Basis for Designing Appropriate Plant Sterol-Enriched Food in Indonesia. Nutrients 2021, 13, 452.
  10. Othman, R.A.; Moghadasian, M.H. Beyond cholesterol-lowering effects of plant sterols: Clinical and experimental evidence of anti-inflammatory properties. Nutr. Rev. 2011, 69, 371–382.
  11. Berger, A.; Jones, P.J.; Abumweis, S.S. Plant sterols: Factors affecting their efficacy and safety as functional food ingredients. Lipids Health Dis. 2004, 3, 5.
  12. Abumweis, S.S.; Barake, R.; Jones, P.J. Plant sterols/stanols as cholesterol lowering agents: A meta-analysis of randomized controlled trials. Food Nutr. Res. 2008, 52.
  13. Demonty, I.; Ras, R.T.; Van der Knaap, H.C.; Duchateau, G.S.; Meijer, L.; Zock, P.L.; Geleijnse, J.M.; Trautwein, E.A. Continuous dose-response relationship of the LDL-cholesterol-lowering effect of phytosterol intake. J. Nutr. 2009, 139, 271–284.
  14. Musa-Veloso, K.; Paulionis, L.; Poon, T.; Lee, H.Y. The effects of almond consumption on fasting blood lipid levels: A systematic review and meta-analysis of randomised controlled trials. J. Nutr. Sci. 2016, 5, e34.
  15. Genser, B.; Silbernagel, G.; De Backer, G.; Bruckert, E.; Carmena, R.; Chapman, M.J.; Deanfield, J.; Descamps, O.S.; Rietzschel, E.R.; Dias, K.C.; et al. Plant sterols and cardiovascular disease: A systematic review and meta-analysis. Eur. Heart J. 2012, 33, 444–451.
  16. Talati, R.; Sobieraj, D.M.; Makanji, S.S.; Phung, O.J.; Coleman, C.I. The comparative efficacy of plant sterols and stanols on serum lipids: A systematic review and meta-analysis. J. Am. Diet. Assoc. 2010, 110, 719–726.
  17. Naumann, E.; Plat, J.; Mensink, R.P. Changes in serum concentrations of noncholesterol sterols and lipoproteins in healthy subjects do not depend on the ratio of plant sterols to stanols in the diet. J. Nutr. 2003, 133, 2741–2747.
  18. Kothari, S.; Dhami-Shah, H.; Shah, S.R. Antidiabetic Drugs and Statins in Nonalcoholic Fatty Liver Disease. J. Clin. Exp. Hepatol. 2019, 9, 723–730.
  19. Choudhury, H.; Pandey, M.; Hua, C.K.; Mun, C.S.; Jing, J.K.; Kong, L.; Ern, L.Y.; Ashraf, N.A.; Kit, S.W.; Yee, T.S.; et al. An update on natural compounds in the remedy of diabetes mellitus: A systematic review. J. Tradit. Complement. Med. 2017, 8, 361–376.
  20. Govindappa, M. A review on the role of plant(s) extracts and its phytochemicals for the management of diabetes. J. Diabetes Metab. 2015, 6, 1–38.
  21. Modak, M.; Dixit, P.; Londhe, J.; Ghaskadbi, S.; Devasagayam, T.P. Indian herbs and herbal drugs used for the treatment of diabetes. J. Clin. Biochem. Nutr. 2007, 40, 163–173.
  22. Aggarwal, N. A Review of Recent Investigations on Medicinal Herbs Possessing Anti-Diabetic Properties. J. Nutr. Disord. Ther. 2011, 1, 2.
  23. Mentreddy, S.R. Medicinal plant species with potential anti-diabetic properties. J. Sci. Food Agric. 2007, 87, 743–750.
  24. Governa, P.; Baini, G.; Borgonetti, V.; Cettolin, G.; Giachetti, D.; Magnano, A.R.; Miraldi, E.; Biagi, M. Phytotherapy in the Management of Diabetes: A Review. Molecules 2018, 23, 105.
  25. Gaikwad, B.S.; Krishna Mohan, G.; Sandhya Rani, M. Phytochemicals for diabetes management. Pharm. Crop. 2014, 5, 11–28.
  26. Dembinska-Kiec, A.; Mykkänen, O.; Kiec-Wilk, B.; Mykkänen, H. Antioxidant phytochemicals against type 2 diabetes. Br. J. Nutr. 2008, 99, 109–117.
  27. Lee, Y.M.; Gweon, O.C.; Seo, Y.J.; Im, J.; Kang, M.J.; Kim, M.J.; Kim, J.I. Antioxidant effect of garlic and aged black garlic in animal model of type 2 diabetes mellitus. Nutr. Res. Pract. 2009, 3, 156–161.
  28. Tiwari, A.K.; Rao, J.M. Diabetes mellitus and multiple therapeutic approaches of phytochemicals: Present status and future prospects. Curr. Sci. 2002, 83, 30–38.
  29. Zhang, X.; Yang, S.; Chen, J.; Su, Z. Unraveling the Regulation of Hepatic Gluconeogenesis. Front. Endocrinol. 2019, 9, 802.
  30. Misawa, E.; Tanaka, M.; Nomaguchi, K.; Yamada, M.; Toida, T.; Takase, M.; Iwatsuki, K.; Kawada, T. Administration of phytosterols isolated from Aloe vera gel reduce visceral fat mass and improve hyperglycemia in Zucker diabetic fatty (ZDF) rats. Obes. Res. Clin. Pract. 2008, 2, 239–245.
  31. Patil, S.B.; Takalikar, S.S.; Joglekar, M.M.; Haldavnekar, V.S.; Arvindekar, A.U. Insulinotropic and β-cell protective action of cuminaldehyde, cuminol and an inhibitor isolated from Cuminumcyminum in streptozotocin-induced diabetic rats. Br. J. Nutr. 2013, 110, 1434–1443.
  32. Meddah, B.; Ducroc, R.; El Abbes Faouzi, M.; Eto, B.; Mahraoui, L.; Benhaddou-Andaloussi, A.; Martineau, L.C.; Cherrah, Y.; Haddad, P.S. Nigella sativa inhibits intestinal glucose absorption and improves glucose tolerance in rats. J. Ethnopharmacol. 2009, 121, 419–424.
  33. Jayaprasad, B.; Sharavanan, P.S.; Sivaraj, R. Antidiabetic effect of Chloroxylonswietenia bark extracts on streptozotocin-induced diabetic rats. Beni-Suef Univ. J. Basic Appl. Sci. 2016, 5, 61–69.
  34. Zhang, Y.; Feng, F.; Chen, T.; Li, Z.; Shen, Q.W. Antidiabetic and antihyperlipidemic activities of Forsythia suspensa (Thunb.) Vahl (fruit) in streptozotocin-induced diabetes mice. J. Ethnopharmacol. 2016, 192, 256–263.
  35. Mohammed, S.I.; Chopda, M.Z.; Patil, R.H.; Vishwakarma, K.S.; Maheshwari, V.L. In vivo anti-diabetic and anti-oxidant activities of Coccinia grandis leaf extract against streptozotocin-induced diabetes in experimental rats. Asian Pac. J. Trop. Dis. 2016, 6, 298–304.
  36. Ahangarpour, A.; Mohammadian, M.; Dianat, M. Antidiabetic effect of hydro-alcholic urtica dioica leaf extract in male rats with fructose-induced insulin resistance. Iran J. Med. Sci. 2012, 37, 181–186.
  37. Jaiswal, Y.S.; Tatke, P.A.; Gabhe, S.Y.; Vaidya, A.B. Antidiabetic activity of extracts of Anacardium occidentale Linn. leaves on n-streptozotocin diabetic rats. J. Tradit. Complement. Med. 2016, 7, 421–427.
  38. Liu, C.T.; Hsu, T.W.; Chen, K.M.; Tan, Y.P.; Lii, C.K.; Sheen, L.Y. The Antidiabetic Effect of Garlic Oil is Associated with Ameliorated Oxidative Stress but Not Ameliorated Level of Pro-inflammatory Cytokines in Skeletal Muscle of Streptozotocin-induced Diabetic Rats. J. Tradit. Complement. Med. 2012, 2, 135–144.
  39. Antu, K.A.; Riya, M.P.; Nair, A.; Mishra, A.; Srivastava, A.K.; Raghu, K.G. Symplocos cochinchinensis enhances insulin sensitivity via the down regulation of lipogenesis and insulin resistance in high energy diet rat model. J. Ethnopharmacol. 2016, 193, 500–509.
  40. Hu, X.; Cheng, D.; Zhang, Z. Antidiabetic activity of Helicteresangustifolia root. Pharm. Biol. 2016, 54, 938–944.
  41. Huang, H.Y.; Korivi, M.; Yang, H.T.; Huang, C.C.; Chaing, Y.Y.; Tsai, Y.C. Effect of Pleurotus tuber-regium polysaccharides supplementation on the progression of diabetes complications in obese-diabetic rats. Chin. J. Physiol. 2014, 57, 198–208.
  42. Oyedemi, S.O.; Adewusi, E.A.; Aiyegoro, O.A.; Akinpelu, D.A. Antidiabetic and haematological effect of aqueous extract of stem bark of Afzelia africana (Smith) on streptozotocin-induced diabetic Wistar rats. Asian Pac. J. Trop. Biomed. 2011, 1, 353–358.
  43. Emordi, J.E.; Agbaje, E.O.; Oreagba, I.A.; Iribhogbe, O.I. Antidiabetic and hypolipidemic activities of hydroethanolic root extract of Uvariachamae in streptozotocin induced diabetic albino rats. BMC Complement. Altern. Med. 2016, 16, 468.
  44. Palsamy, P.; Subramanian, S. Resveratrol, a natural phytoalexin, normalizes hyperglycemia in streptozotocin-nicotinamide induced experimental diabetic rats. Biomed. Pharmacother. 2008, 62, 598–605.
  45. El-Beshbishy, H.; Bahashwan, S. Hypoglycemic effect of basil (Ocimum basilicum) aqueous extract is mediated through inhibition of α-glucosidase and α-amylase activities: An in vitro study. Toxicol. Ind. Health 2012, 28, 42–50.
  46. Abubakar, A.R.; Haque, M. Preparation of Medicinal Plants: Basic Extraction and Fractionation Procedures for Experimental Purposes. J. Pharm. Bioallied Sci. 2020, 12, 1–10.
  47. Oboh, G.; Ademiluyi, A.O.; Akinyemi, A.J.; Henle, T.; Saliu, J.A.; Schwarzenbolz, U. Inhibitory effect of polyphenol-rich extracts of jute leaf (Corchorus olitorius) on key enzyme linked to type 2 diabetes (α-amylase and α-glucosidase) and hypertension (angiotensin I converting) in vitro. J. Funct. Foods 2012, 4, 450–458.
  48. Ademiluyi, A.O.; Oboh, G.; Aragbaiye, F.P.; Oyeleye, S.I.; Ogunsuyi, O.B. Antioxidant properties and in vitro α-amylase and α-glucosidase inhibitory properties of phenolics constituents from different varieties of Corchorus spp. J. Taibah Univ. Med. Sci. 2015, 10, 278–287.
  49. Ademiluyi, A.O.; Oboh, G. Soybean phenolic-rich extracts inhibit key-enzymes linked to type 2 diabetes (α-amylase and α-glucosidase) and hypertension (angiotensin I converting enzyme) in vitro. Exp. Toxicol. Pathol. 2013, 65, 305–309.
  50. Choo, C.Y.; Sulong, N.Y.; Man, F.; Wong, T.W. Vitexin and isovitexin from the leaves of Ficusdeltoidea with in-vivo α-glucosidase inhibition. J. Ethnopharmacol. 2012, 142, 776–781.
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