Kumari Kumud, Augusti K T
Department of Biochemistry, University of Kerala, Kariavattom, Thiruvananthapuram 695581, India.
Indian J Exp Biol. 2002 Sep;40(9):1005-9.
Antidiabetic and antoxidant effects of S-methyl cysteine sulfoxide (SMCS) isolated from A. cepa and two standard drugs, glibenclamide and insulin were studied and compared in alloxan diabetic rats after using each of them for treatment for two months. These drugs ameliorated the diabetic condition significantly, viz. maintenance of body weight and control of blood sugar in rats. Further they lowered the levels of malondialdehyde, hydroperoxide and conjugated dienes in tissues exhibiting antioxidant effect on lipid peroxidation in experimental diabetes. This is achieved by their stimulating effects on glucose utilization and the antioxidant enzymes, viz. superoxide dismutase and catalase. The probable mechanism of action of SMCS and glibenclamide may be partly dependent on the stimulation of insulin secretions and partly due to their individual actions. In the amelioration of diabetes the standard drugs showed a better action, but as an antioxidant SMCS proved to be a better one.
从洋葱中分离出的S-甲基半胱氨酸亚砜(SMCS)以及两种标准药物格列本脲和胰岛素的抗糖尿病和抗氧化作用,在给四氧嘧啶诱导的糖尿病大鼠使用两个月后进行了研究和比较。这些药物显著改善了糖尿病状况,即维持了大鼠体重并控制了血糖。此外,它们降低了组织中丙二醛、氢过氧化物和共轭二烯的水平,对实验性糖尿病中的脂质过氧化表现出抗氧化作用。这是通过它们对葡萄糖利用和抗氧化酶(即超氧化物歧化酶和过氧化氢酶)的刺激作用实现的。SMCS和格列本脲可能的作用机制可能部分取决于对胰岛素分泌的刺激,部分归因于它们各自的作用。在改善糖尿病方面,标准药物显示出更好的效果,但作为抗氧化剂,SMCS被证明效果更佳。