黄芪甲苷
内科学
内分泌学
葡萄糖6-磷酸酶
链脲佐菌素
葡萄糖稳态
甘油三酯
胰岛素
糖原
糖尿病
酶
糖原分解
糖原磷酸化酶
医学
化学
药理学
胆固醇
生物化学
胰岛素抵抗
色谱法
高效液相色谱法
作者
Lin Lv,Shaoyu Wu,Guangfa Wang,Jiajie Zhang,Jianxin Pang,Zhong‐Qiu Liu,Wei Xu,Shuguang Wu,Jinjun Rao
摘要
Abstract Aim: Hepatic glycogen phosphorylase (GP) and glucose‐6‐phosphatase (G6Pase) are important in control of blood glucose homeostasis, and are considered to be potential targets for antidiabetic drugs. Astragaloside IV has been reported to have a hypoglycemic effect. However, the biochemical mechanisms by which astragaloside IV regulates hepatic glucose‐metabolizing enzymes remain unknown. The present study examines whether GP and G6Pase mediate the hypoglycemic effect of astragaloside IV. Methods: Type 2 diabetic mice were treated with astragaloside IV for 2 weeks. Blood glucose and insulin levels were measured by a glucometer and the ELISA method, respectively. Total cholesterol (TC) and triglyceride (TG) levels were determined using Labassay TM kits. Activities of hepatic GP and G6Pase were measured by the glucose‐6‐phosphate dehydrogenase‐coupled reaction. The mRNA and protein levels of both enzymes were determined by real‐time RT‐PCR and Western blotting. Results: Astragaloside IV at 25 and 50 mg/kg significally decreased the blood glucose, TG and insulin levels, and inhibited the mRNA and protein expression as well as enzyme activity of GP and G6Pase in diabetic mice. Conclusions: Astragaloside IV exhibited a hypoglycemic effect in diabetic mice. The hypoglycemic effect of this compound may be explained, in part, by its inhibition of hepatic GP and G6Pase activities. Copyright © 2009 John Wiley & Sons, Ltd.
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