1. Cheng D. Prevalence, predisposition and prevention of type II diabetes. Nutr Metab (Lond). 2005. 2:29.
Article
2. American Diabetes Association (ADA). Summary of revisions for the 2008 clinical practice recommendations. Diabetes Care. 2008. 31:S3–S4.
3. Lorenzati B, Zucco C, Miglietta S, Lamberti F, Bruno G. Oral hypoglycemic drugs: Pathophysiological basis of their mechanism of action. Pharmaceuticals. 2010. 3:3005–3020.
Article
4. Adewole SO, Caxton-Martins EA, Ojewole JAO. Protective effect of quercetin on the morphology of pancreatic β-cells of streptozotocin-treated diabetic rats. Afr J Tradit Complement Altern Med. 2006. 4:64–74.
Article
5. Coskun O, Kanter M, Korkmaz A, Oter S. Quercetin, a flavonoid antioxidant, prevents and protects streptozotocin-induced oxidative stress and β-cell damage in rat pancreas. Pharmacol Res. 2005. 51:117–123.
Article
6. Shetty AK, Rashmi R, Rajan MGR, Sambaiah K, Salimath PV. Antidiabetic influence of quercetin in streptozotocin-induced diabetic rats. Nutr Res. 2004. 24:373–381.
Article
7. Ramachandra R, Shetty AK, Salimath PV. Quercetin alleviates activities of intestinal and renal disaccharidases in streptozotocin-induced diabetic rats. Mol Nutr Food Res. 2005. 49:355–360.
Article
8. Anjaneyulu M, Chopra K. Quercetin, an anti-oxidant bioflavonoid, attenuates diabetic nephropathy in rats. Clin Exp Pharmacol Physiol. 2004. 31:244–248.
Article
9. Ishikawa A, Yamashita H, Hiemori M, Inagaki E, Kimoto M, Okamoto M, Tsuji H, Memon AN, Mohammadio A, Natori Y. Characterization of inhibitors of postprandial hyperglycemia from the leaves of
Nerium indicum. J Nutr Sci Vitaminol (Tokyo). 2007. 53:166–173.
Article
10. Jo SH, Ka EH, Lee HS, Apostolidis E, Jang HD, Kwon YI. Comparison of antioxidant potential and rat intestinal α-glucosidases inihibitory activities of quercetin, rutin, and isoquercetin. Int J Appl Res Nat Prod. 2009. 2:52–60.
11. Standl E, Baumgartl HJ, Füchtenbusch M, Stemplinger J. Effect of acarbose on additional insulin therapy in type 2 diabetic patients with late failure of sulphonylurea therapy. Diabetes Obes Metab. 1999. 1:215–220.
Article
12. Abrahamson MJ. Optimal glycemic control in type 2 diabetes mellitus: Fasting and postprandial glucose in context. Arch Intern Med. 2004. 164:486–491.
Article
13. Kim YM, Jeong YK, Wang MH, Lee WY, Rhee HI. Inhibitory effect of pine extract on α-glucosidase activity and postprandial hyperglycemia. Nutrition. 2005. 21:756–761.
Article
14. Tsujita T, Takaku T. Mechanism of the inhibitory action of chestnut astringent skin extract on carbohydrate absorption. J Nutr Sci Vitaminol (Tokyo). 2008. 54:416–421.
Article
15. Akbarzadeh A, Norouzian D, Mehrabi MR, Jamshidi Sh, Farhangi A, Allah Verdi A, Mofidian SMA, Lame Rad B. Induction of diabetes by streptozotocin in rats. Indian J Clin Biochem. 2007. 22:60–64.
Article
16. Lee SK, Hwang JY, Song JH, Jo JR, Kim MJ, Kim ME, Kim JI. Inhibitory activity of Euonymus alatus against alpha-glucosidase in vitro and in vivo. Nutr Res Pract. 2007. 1:184–188.
17. Raabo E, Terkildsen TC. On the enzymatic determination of blood glucose. Scand J Clin Lab Invest. 1960. 12:402–407.
Article
18. Reeves PG, Nielsen FH, Fahey GC Jr. AIN-93 purified diets for laboratory rodents: final report of the American Institute of Nutrition ad hoc writing committee on the reformulation of the AIN-76A rodent diet. J Nutr. 1993. 123:1939–1951.
Article
19. Schifreen RS, Hickingbotham JM, Bowers GN Jr. Accuracy, precision, and stability in measurement of hemoglobin A
1c by "high-performance" cation-exchange chromatography. Clin Chem. 1980. 26:466–472.
Article
20. Morgan CR, Lazarow A. Immunoassay of insulin: Two antibody system. Plasma insulin levels in normal, subdiabetic, and diabetic rats. Diabetes. 1963. 12:115–126.
Article
21. Dahlqvist A. Assay of intestinal disaccharidases. Scand J Clin Lab Invest. 1984. 44:169–172.
Article
22. Lowry OH, Rosenbrough NJ, Farr AL, Randall RJ. Protein measurement with the Folin phenol reagent. J Biol Chem. 1951. 193:265–275.
Article
23. Madar Z. The effect of acarbose and miglitol (BAY-M-1099) on postprandial glucose levels following ingestion of various sources of starch by nondiabetic and streptozotocin-induced diabetic rats. J Nutr. 1989. 119:2023–2029.
Article
24. Kang MJ, Kim JH, Choi HN, Kim MJ, Han JH, Lee JH, Kim JI. Hypoglycemic effects of Welsh onion in animal model of diabetes mellitus. Nutr Res Pract. 2010. 4:486–491.
Article
25. Ceriello A. Postprandial hyperglycemia and diabetes complications: is it time to treat? Diabetes. 2005. 54:1–7.
26. Ishida H, Takizawa M, Ozawa S, Nakamichi Y, Yamaguchi S, Katsuta H, Tanaka T, Maruyama M, Katahira H, Yoshimoto K, Itagaki E, Nagamatsu S. Pioglitazone improves insulin secretory capacity and prevents the loss of β-cell mass in obese diabetic db/db mice: Possible protection of β cells from oxidative stress. Metabolism. 2004. 53:488–494.
Article
27. Srinivasan K, Ramarao P. Animal models in type 2 diabetes research: an overview. Indian J Med Res. 2007. 125:451–472.
28. Hummel KP, Coleman DL, Lane PW. The influence of genetic background on expression of mutations at the diabetes locus in the mouse. I. C57BL/KsJ and C57BL/6J strains. Biochem Genet. 1972. 7:1–13.
Article
29. Dimitriadis GD, Tessari P, Go VLW, Gerich JE. α-Glucosidase inhibition improves postprandial hyperglycemia and decreases insulin requirements in insulin-dependent diabetes mellitus. Metabolism. 1985. 34:261–265.
Article
30. Carrascosa JM, Molero JC, Fermín Y, Martínez C, Andrés A, Satrústegui J. Effects of chronic treatment with acarbose on glucose and lipid metabolism in obese diabetic Wistar rats. Diabetes Obes Metab. 2001. 3:240–248.
Article
31. Kannappan S, Anuradha CV. Insulin sensitizing actions of fenugreek seed polyphenols, quercetin & metformin in a rat model. Indian J Med Res. 2009. 129:401–408.
32. Juretić D, Bernik Š, Čop L, Hadžija M, Petlevski R, Lukač-Bajalo J. Short-term effect of acarbose on specific intestinal disaccharidase activities and hyperglycaemia in CBA diabetic mice. J Anim Physiol Anim Nutr (Berl). 2003. 87:263–268.
Article
33. Lee SM, Bustamante S, Flores C, Bezerra J, Goda T, Koldovský O. Chronic effects of an α-glucosidase inhibitor (Bay o 1248) on intestinal disaccharidase activity in normal and diabetic mice. J Pharmacol Exp Ther. 1987. 240:132–137.
34. Liu L, Yu YL, Yang JS, Li Y, Liu YW, Liang Y, Liu XD, Xie L, Wang GJ. Berberine suppresses intestinal disaccharidases with beneficial metabolic effects in diabetic states, evidences from
in vivo and
in vitro study. Naunyn Schmiedebergs Arch Pharmacol. 2010. 381:371–381.
Article
35. Bressler R, Johnson D. New pharmacological approaches to therapy of NIDDM. Diabetes Care. 1992. 15:792–805.
Article
36. Theoharides TC, Bielory L. Mast cells and mast cell mediators as targets of dietary supplements. Ann Allergy Asthma Immunol. 2004. 93:S24–S34.
Article