Chi Tzong-Cherng, Chen Win-Pin, Chi Tsung-Li, Kuo Tzong-Fu, Lee Shoei-Sheng, Cheng Juei-Tang, Su Ming-Jai
Institute of Pharmacology, College of Medicine, National Taiwan University, No 1, Sec 1, Jen-Ai Rd, Taipei, Taiwan.
Life Sci. 2007 Apr 10;80(18):1713-20. doi: 10.1016/j.lfs.2007.02.002. Epub 2007 Feb 9.
Resveratrol, a polyphenolic substance found in grape skin, is proposed to account in part for the protective effect of red wine in the cardiovascular system. The aim of the present study is to investigate the action and possible mechanisms of resveratrol-produced regulation of plasma glucose in normal and diabetic rats including the animal model of streptozotocin (STZ)-induced and nicotinamide-STZ-induced (NA-STZ), and insulin-resistant diabetic rats. Resveratrol (p.o.) produced a hypoglycemic effect in a dose-dependent manner in normal and diabetic rats, and the insulin level was increased following resveratrol treatment in normal and NA-STZ diabetic rats. In insulin-deficient STZ-diabetic rats, resveratrol significantly lowered the plasma glucose 90 min after oral treatment, and the hypoglycemic effect was abolished by phosphatidyl-3-kinase (PI3K) inhibitors (LY294002 and wortmannin) which also inhibited resveratrol-induced Akt phosphorylation in soleus muscle of STZ-diabetic rats. The change in the protein expression level of glucose transporter subtype 4 (GLUT4) in the soleus muscle and phosphoenolpyruvate carboxykinase (PEPCK) in the liver of STZ-diabetic rats treated with resveratrol (3 mg/kg, p.o.) for 7 days was examined. Resveratrol normalized hepatic PEPCK expression and increased GLUT4 expression in the soleus muscle of STZ-diabetic rats. The results indicate that the mechanisms contributing to the hypoglycemic effect of resveratrol include insulin-dependent and insulin-independent pathway, and PI3K-Akt-signaling was involved in the latter mechanism to enhance glucose uptake in skeletal muscle.
白藜芦醇是一种存在于葡萄皮中的多酚类物质,有人认为它在一定程度上解释了红酒对心血管系统的保护作用。本研究的目的是探讨白藜芦醇对正常大鼠和糖尿病大鼠(包括链脲佐菌素(STZ)诱导和烟酰胺-STZ诱导(NA-STZ)的动物模型以及胰岛素抵抗糖尿病大鼠)血浆葡萄糖调节的作用及可能机制。白藜芦醇(口服)在正常大鼠和糖尿病大鼠中均呈剂量依赖性地产生降血糖作用,在正常大鼠和NA-STZ糖尿病大鼠中,白藜芦醇治疗后胰岛素水平升高。在胰岛素缺乏的STZ糖尿病大鼠中,口服白藜芦醇90分钟后可显著降低血浆葡萄糖水平,磷脂酰-3-激酶(PI3K)抑制剂(LY294002和渥曼青霉素)可消除这种降血糖作用,这些抑制剂还抑制了STZ糖尿病大鼠比目鱼肌中白藜芦醇诱导的Akt磷酸化。检测了用白藜芦醇(3mg/kg,口服)处理7天的STZ糖尿病大鼠比目鱼肌中葡萄糖转运蛋白亚型4(GLUT4)和肝脏中磷酸烯醇式丙酮酸羧激酶(PEPCK)蛋白表达水平的变化。白藜芦醇使STZ糖尿病大鼠肝脏中PEPCK表达正常化,并增加了比目鱼肌中GLUT4的表达。结果表明,白藜芦醇降血糖作用的机制包括胰岛素依赖和非胰岛素依赖途径,PI3K-Akt信号通路参与了后一种机制,以增强骨骼肌对葡萄糖的摄取。