INTRODUCTIONDiabetes mellitus is a chronic metabolic disorder that occurs due to deficiency of insulin action. There are various causes of diabetes mellitus -destruction of beta cells of pancreas (Type 1 DM) or resistance to insulin action (Type 2 DM), etc. Irrespective of the cause, diabetes mellitus is characterized by hyperglycemia and altered metabolisms of carbohydrates, lipids and amino acids. 1 Diabetes mellitus has been one of the greatest public health problem over the years throughout the world. It is one of the leading contributor to death and is ranked at 3 rd position. International Diabetes Federation predicts that approximately 592 million individuals will have diabetes by 2035.
2,3Diabetes mellitus if not controlled results in complications like obesity, renal failure, retinopathy, neuropathy, etc. Strict maintenance of euglycaemia is mandatory to prevent complications which can be attained by exogenous insulin and/or oral hypoglycaemic drugs. All the current medications for diabetes mellitus are not devoid of adverse effects, as a result patient are prone to develop a new disease at the cost of getting treated for diabetes mellitus. Resistance to these drugs over prolonged periods adds ABSTRACT Background: To evaluate hypoglycemic activity of methanolic extract of roots of Acorus calamus (AC) in alloxan induced diabetic albino rats and to compare with standard oral hypoglycemic drug glibenclamide. Methods: A total of 54 rats were used for this study. The study was done in two phases. In phase I, oral glucose tolerance test was done in 4 groups at 0, 30, 60 and 120 minutes after administration of AC in 3 different doses -100, 150 and 200mg/kg to 3 different groups, with control being the fourth group. The dose of AC which caused maximal blood glucose lowering was selected for phase II. In phase II, rats were divided into 5 groups. First 2 groups were non diabetic groups which were given distilled water (DW) and AC respectively. Next 3 groups were alloxan induced diabetic groups which were given DW, AC and Glibencamide 0.5mg/kg po respectively. All drugs were given for 28 days and FBS was measured on 0, 3, 7, 14, 21, and 28 th days. Results: In phase I, both AC 150 and 200mg/kg lowered blood glucose but their effect was comparable and thus lower dose -150mg/kg was selected for phase II. In phase II, among non-diabetic groups, AC 150 mg/kg produced significant hypoglycemia in comparison with control group. Among diabetic groups, both AC 150 mg/kg and glibenclamide 0.5 mg/kg produced significant hypoglycemia in comparison with control group on all days. On days 3 and 7, hypoglycaemic action of AC 150mg/kg was not as much as Glibenclamide (p <0.05), but on days 14, 21 and 28, the hypoglycaemic action of AC 150 mg/kg was comparable to Glibenclamide 0.5mg/kg. (P >0.05). Conclusions: AC 150mg/kg causes hypoglycemia in alloxan induced diabetic rats as well as nondiabetic rats.