Evaluation of antihyperglycemic and antioxidant properties of Streblus asper Lour against streptozotocin–induced diabetes in rats

• Published in: Asian Pacific journal of tropical disease Vol. 2; no. 2; pp. 139 - 143
• Main Authors: Kumar, RB Suresh, Kar, Biswakanth, Dolai, Narayan, Bala, Asis, Haldar, Pallab Kanti
• Format: Journal Article
• Language: English
• Published: Elsevier B.V 01.04.2012
• Subjects: Antidiabetic; Antioxidant; Diabetes mellitus; Glibenclamide; Lipid peroxide; Oxidative stress; Streblus asper; Streptozotocin; Streblus asper; Oxidative stress; Antidiabetic; Diabetes mellitus; Lipid peroxide; Glibenclamide; Antioxidant; Streptozotocin
• ISSN: 2222-1808; 2222-1808
• DOI: 10.1016/S2222-1808(12)60032-2

To evaluate antidiabetic and antioxidant role of methanol extract of Streblus asper (S. asper) root bark in Wistar rats. Diabetes was induced in rats by single intraperitoneal injection of streptozotocin (STZ, 65 mg/kg body weight). Three days after STZ induction, the diabetic rats were treated with S. asper orally at dose of 200 and 400 mg/kg body weight daily for 15 days. Glibenclamide (0.25 mg/kg, orally) was used as reference drug. The fasting blood glucose levels were measured on every fifth day during the 15-day treatment. Serum biochemical parameters such as serum glutamate pyruvate transaminase, serum glutamate oxaloacetate transaminase, serum alkaline phosphatase, total cholesterol total protein and serum triglycerides were estimated. Antioxidant properties were assessed by estimating liver and kidney thiobarbituric acid reactive substances, reduced glutathione and catalase. S. asper in STZ-induced diabetic rats, at doses of 200 and 400 mg/kg bw produced reduction in blood glucose levels when compared with the STZ control group. Serum biochemical parameters antioxidant levels were significantly restored toward normal levels in S. asper treated rats as compared with STZ control. The present study infers that the methanol extract of S. asper root bark demonstrated remarkable antidiabetic activity in STZ-induced diabetic rats. The potential antidiabetic action is plausibly due to its underlying antioxidant role.