Hoich R I, Ng F M
Pharmacol Res Commun. 1986 May;18(5):419-30. doi: 10.1016/0031-6989(86)90163-3.
Normal rats were given a daily dose of gliclazide (8 mg/kg) for a period of 6 days. Twenty-four hours after the treatment period, the treated animals had a significant increase in the initial rate of glucose utilization during intravenous glucose tolerance tests when compared to the controls. Insulin-stimulated 3-0-Methylglucose transport and glucose oxidation were potentiated in adipocytes prepared from gliclazide-treated rats, indicating that improved glycemic control can, at least partly, be attributed to extrapancreatic effects. The drug treatment did not induce any changes in total insulin binding, implicating that the extrapancreatic effects of this hypoglycemic drug are mediated through a post-binding site.
正常大鼠连续6天每日给予格列齐特(8毫克/千克)。治疗期结束24小时后,与对照组相比,接受治疗的动物在静脉葡萄糖耐量试验期间葡萄糖利用的初始速率显著增加。在格列齐特治疗的大鼠制备的脂肪细胞中,胰岛素刺激的3-0-甲基葡萄糖转运和葡萄糖氧化增强,这表明血糖控制的改善至少部分可归因于胰腺外效应。药物治疗未引起总胰岛素结合的任何变化,这意味着这种降糖药物的胰腺外效应是通过结合后位点介导的。