Hypoglycemic and hypolipidemic effects of Saururus chinensis Baill in streptozotocin-induced diabetic rats

  • Hwang, Ji-Yeon (Biohealth Product Research Center, School of Food and Life Science, Institute for Food Sciences, Institute of Biomedical Engineering, Inje University) ;
  • Zhang, Jian (Biohealth Product Research Center, School of Food and Life Science, Institute for Food Sciences, Institute of Biomedical Engineering, Inje University) ;
  • Kang, Min-Jung (Biohealth Product Research Center, School of Food and Life Science, Institute for Food Sciences, Institute of Biomedical Engineering, Inje University) ;
  • Lee, Soo-Kyung (Biohealth Product Research Center, School of Food and Life Science, Institute for Food Sciences, Institute of Biomedical Engineering, Inje University) ;
  • Kim, Hyun-A (Amicogen Inc.) ;
  • Kim, Jong-Jin (Amicogen Inc.) ;
  • Kim, Jung-In (Biohealth Product Research Center, School of Food and Life Science, Institute for Food Sciences, Institute of Biomedical Engineering, Inje University)
  • 발행 : 2007.06.20

초록

Saururus chinensis Baill was reported to inhibit ${\alpha}-glucosidase$ in vitro and flatten postprandial increase in blood glucose in streptozotocin (STZ)-induced diabetic rats. We studied the effect of chronic consumption of S. chinensis Baill on blood glucose and lipid profile in STZ-induced diabetic male rats fed high fat diet. Male rats weighing 100-120 g were fed 30% fat diet with and without 10% freeze-dried leaves of S. chinensis Baill for 7 weeks after 1 week of adaptation. The rats were rendered diabetic by intravenous injection of STZ (60 mg/kg) after 6-week feeding of the assigned diets. At 1 week after the injection, the rats were sacrificed after an overnight fast. Plasma glucose ($380.2{\pm}14.4mg/dL$), total cholesterol ($93.9{\pm}7.9mg/dL$) and triglyceride levels ($123.6{\pm}7.5mg/dL$) of the S. chinensis Baill group were significantly lower than those of the control group ($418.1{\pm}12.0mg/dL,\;119.9{\pm}9.4mg/dL,\;152.0{\pm}10.3mg/dL$, respectively, p<0.05). Chronic consumption of S. chinesis Baill significantly decreased maltase activity of the small intestinal mucosa ($120.1{\pm}8.7U/g$) protein compared with the control group ($96.8{\pm}7.0U/g protein, p<0.05). These results suggest that S. chinensis Baill have hypoglycemic and hypolipidemic effects by inhibiting ${\alpha}-glucosidase$ activity in the animal model of diabetes mellitus.

키워드

참고문헌

  1. American Diabetes Association (2003). Management of dyslipidemia in adults with diabetes. Diabetes Care 26:S83-S86 https://doi.org/10.2337/diacare.26.2007.S83
  2. A.O.A.C. (1995). Official methods of analysis. 14th ed. Association of official analytical chemists, Washington DC. USA
  3. Azuma K, Toyofuku Y, Iesaki T, Otsuka A, Tanaka A, Mita T, Hirose T, Tanaka Y, Daida H, Kawamori R & Watada H (2006). Acarbose, an alpha-glucosidase inhibitor, improves endothelial dysfunction in Goto-Kakizaki rats exhibiting repetitive blood glucose fluctuation. Biochem Biophys Res Commun 345:688-693 https://doi.org/10.1016/j.bbrc.2006.04.090
  4. Balflour JA & McTavish D (1993). Acarbose. An update of its pharmacology and therapeutic use in diabetes mellitus. Drugs 46:1025-1054 https://doi.org/10.2165/00003495-199346060-00007
  5. Centers for Disease Control and Prevention (1999). Diabetes Surveillance Report, Atlanta, GA: US Department of Health and Human Services
  6. Chung BS & Shin MG (1990). Dictionary of Korean Folk Medicine, p.813. Young Lim Sa, Seoul. Republic of Korea
  7. Coniff RF, Shapiro JA, Robbins D, Kleinfield R, Seaton TB, Beisswenger P & McGill JB (1995). Reduction of glycosylated hemoglobin and postprandial hyperglycemia by acarbose in patients with NIDDM. Diabetes Care 18:817-824 https://doi.org/10.2337/diacare.18.6.817
  8. Dahlqvist A (1984). Assay of intestinal disaccharidases. Scand J Clin Lab Invest 44:169-172 https://doi.org/10.3109/00365518409161400
  9. Fujita H & Yamagami T (2001). Fermented soybean-derived touchiextract with anti-diabetic effect via alpha-glucosidase inhibitory action in a long-term administration study with KKAy mice. Life Sci 70:219-227 https://doi.org/10.1016/S0024-3205(01)01381-9
  10. Fujita H, Yamagami T & Ohshima K (2001). Fermented soybeanderived touchi extract with anti-glycaemic effect via ${\alpha}$-glucosidase inhibitory action in rats and humans. J Nutr 131:1211-1213
  11. Fujita H, Yamagami T & Ohshima K (2003). Long-term ingestion of touchi-extract, ${\alpha}$-glucosidase inhibitor, by borderline and mild type-2 diabetic subjects is safe and significantly reduces blood glucose levels. Nutr Res 23:713-722 https://doi.org/10.1016/S0271-5317(03)00028-9
  12. Hanefeld M (1988). The Role of acarbose in the treatment of non-insulin-dependent diabetes mellitus. J Diabetes Complications 12:228-237 https://doi.org/10.1016/S1056-8727(97)00123-2
  13. Holman RR, Cull CA & Turner RC (1999). A randomized doubleblind trial of acarbose in type 2 diabetes shows improved glycemic control over 3 years (U.K. Prospective Diabetes Study 44) Diabetes Care 22:960-964 https://doi.org/10.2337/diacare.22.6.960
  14. Joo HJ, Kang MJ, Seo TJ, Kim HA, Yoo SJ, Lee SK, Lim HJ, Byun BH & Kim JI (2006). The hypoglycemic effect of S. chinensis Baill in animal models of diabetes mellitus. Food Science and Biotechnology 15:413-417
  15. Juretic D, Bernik S, Cop L, Hadzila M, Petlevski R & Lukac-Bajalo J (2003). Short-term effect of acarbose on specific intestinal disaccharidase activities and hyperglycaemia in CBA diabetic mice. J Anim Physiol Anim Nutr (Berl) 87:263-268 https://doi.org/10.1046/j.1439-0396.2003.00435.x
  16. King H, Aubert RE & Herman WH (1998) Global burden of diabetes, 1995-2025: prevalence, numerical estimates, and projections. Diabetes Care 21:1414-1431 https://doi.org/10.2337/diacare.21.9.1414
  17. Kwon CS, Son KH & Kim JS (2004). Effect of Lonicera japonica flower on body weight gain and glucose tolerance in rodents. Food Science and Biotechnology 13:768-771
  18. Kwon EH, Jang HS, Kim SW, Choi SW, Rhee SJ & Cho SH (2007). Effects of mulberry juice and cake powders on blood glucose and lipid lowering and erythrocyte antioxidative enzyme activities in sterptozotocin-induced diabetic rats. Korean Journal of Nutrition 40:199-210
  19. Lebovitz HE (1998).$ \alpha$-Glucosidase inhibitors as agents in the treatment of diabetes. Diabetes Reviews 6:132-145
  20. Lowry OH, Rosenbrough NJ, Farr AL & Randall RJ (1951). Protein measurement with the Folin phenol reagent. J Biol Chem 193: 265-275
  21. Matsui T, Yoshimoto C, Osajima K, Oki T, Osajima Y, Oki T & Osajima Y (1996). In vitro survey of ${\alpha}$-glucosidase inhibitory food components. Biosci Biotechnol Biochem 60:2019-2022 https://doi.org/10.1271/bbb.60.2019
  22. Mughal MA, Memon MY, Zardari MK, Tanwani RK & Ali M (2000). Effect of acarbose on glycemic control, serum lipids and lipoproteins in type 2 diabetes. J Pak Med Assoc 50:152-156
  23. Murali B, Upadhyaya UM & Goyal RK (2002). Effect of chronic treatment with Enicostemma littorale in non-insulin-dependent diabetic (NIDDM) rats. J Ethnopharmacol 81:199-204 https://doi.org/10.1016/S0378-8741(02)00077-6
  24. Qualmann C, Nauck MA, Holst JJ, Orskov C & Creutzfeldt W (1995). Glucagon-like peptide 1 (7-36 amide) secretion in response to luminal sucrose from the upper and lower gut. A study using alpha-glucosidase inhibition (acarbose). Scand J Gastroenterol 30:892-896 https://doi.org/10.3109/00365529509101597
  25. Saito N, Sakai H, Sekihara H & Yajima Y (1998). Effect of an $ \alpha$ -glucosidase inhibitor (voglibose), in combination with sulphonilureas, on glycaemic control in type 2 diabetes subjects. J Int Med Res 26:219-232 https://doi.org/10.1177/030006059802600501
  26. Seifarth C, Bergmann J, Holst JJ, Ritzel R, Schmiegel W & Nauck MA (1998). Prolonged and enhanced secretion of glucagon-like peptide 1 (7-36 amide) after oral sucrose due to alpha-glucosidase inhibition (acarbose) in type 2 diabetic patients. Diabet Med 15:485-491 https://doi.org/10.1002/(SICI)1096-9136(199806)15:6<485::AID-DIA610>3.0.CO;2-Y
  27. Sels JP, Huijberts MS & Wolffenbuttel BH (1999). Miglitol, a new alpha-glucosidase inhibitor. Expert Opin Pharmacother 1:149-156 https://doi.org/10.1517/14656566.1.1.149
  28. Stand E, Baumgartl HJ, Fuchtenbusch M & Stemplinger J (1999). Effect of acarbose on additional insulin therapy in type 2 diabetic patients with late failure of sulphonylurea therapy. Diabetes Obes Metab 1:215-220 https://doi.org/10.1046/j.1463-1326.1999.00021.x
  29. The Diabetes Control and Complications Trial (DCCT) Research Group (1993). The effect of intensive treatment of diabetes on the development and progression of long-term complications in the diabetes control in insulin-dependent diabetes mellitus. N Engl J Med 329:977-986 https://doi.org/10.1056/NEJM199309303291401
  30. Toeller M (1994). Alpha-glucosidase inhibitors in diabetes: efficacy in NIDDM subjects. Eur J Clin Invest. 24:31-35 https://doi.org/10.1111/j.1365-2362.1994.tb02253.x
  31. UK Prospective Diabetes Study (UKPDS) Group (1998). Tight blood pressure control and risk of macrovascular and microvascular complications in type 2 diabetes. UKPDS 38. BMJ 317:703-713
  32. Watanabe J, Kawabata J, Kurihara H & Niki R (1997). Isolation and identification of $ \alpha$-glucosidase inhibitors from Tochu-cha (Encommia ulmoides). Biosci Biotechnol Biochem 61:177-178 https://doi.org/10.1271/bbb.61.177
  33. Yamashita K, Sugawara S & Sakairi I (1984). Effects of an alpha-glucosidase inhibitor, acarbose, on blood glucose and serum lipids in streptozotocin-induced diabetic rats. Horm Metab Res 16:179-182 https://doi.org/10.1055/s-2007-1014737
  34. Yoo SK, Kim MJ, Kim JW & Rhee SJ (2002). Effects of YK-209 mulberry leasves diasaccharidase activities of small intestine and blood glucose-lowering in sterptozotocin-induced diabetic rats. Journal of the Korean Society Food Science and Nutrition 31:1071-1077 https://doi.org/10.3746/jkfn.2002.31.6.1071
  35. Zavaroni I & Reaven GM (1981). Inhibition of carbohydrate-induced hypertriglyceridemia by a disaccharidase inhibitor. Metabolism 30:417-420 https://doi.org/10.1016/0026-0495(81)90125-6