A-Rahim Y I, Beyer K H, Vesell E S
Department of Pharmacology, Pennsylvania State University College of Medicine, Hershey 17033, USA.
Pharmacology. 1996 Mar;52(3):135-44. doi: 10.1159/000139377.
Pyrazinoylguanidine (PZG) is a new antihyperglycemic, antihyperlipidemic drug. The current study reports on the development of an animal model in which the favorable metabolic effects of PZG, previously described in diabetic patients, could be reproduced and investigated. Adult male as well as female Sprague-Dawley rats received a single intraperitoneal dose (50 mg/kg) of streptozotocin (STZ). One week later, they received PZG (50 mg/kg i.p.) twice daily for a week. Compared to vehicle (saline-treated controls), PZG reduced plasma concentrations of glucose by 33-70%, triglycerides by 50-70%, nonesterified fatty acids by 17-27%, cholesterol by 10-50%, and glucagon by 18-20%. Hydrochlorothiazide given in a dose of 20 mg/kg i.p. b.i.d for 1 week induced metabolic effects opposite to those of PZG. In the Zucker fatty rat, PZG also lowered plasma glucose and lipid concentrations. These results indicate that PZG ameliorated the abnormalities of plasma glucose and lipid that characterize STZ-diabetic and Zucker fatty rats.
吡嗪甲酰胍(PZG)是一种新型的降血糖、降血脂药物。当前的研究报告了一种动物模型的建立,在该模型中,先前在糖尿病患者中所描述的PZG的有益代谢作用能够得以重现并进行研究。成年雄性和雌性斯普拉格-道利大鼠接受单次腹腔注射剂量为50毫克/千克的链脲佐菌素(STZ)。一周后,它们每天接受两次PZG(50毫克/千克腹腔注射),持续一周。与溶媒(生理盐水处理的对照组)相比,PZG使血浆葡萄糖浓度降低了33% - 70%,甘油三酯降低了50% - 70%,非酯化脂肪酸降低了17% - 27%,胆固醇降低了10% - 50%,胰高血糖素降低了18% - 20%。以20毫克/千克腹腔注射、每日两次的剂量给予氢氯噻嗪1周,所诱导的代谢效应与PZG相反。在 Zucker 肥胖大鼠中,PZG也降低了血浆葡萄糖和脂质浓度。这些结果表明,PZG改善了链脲佐菌素诱导的糖尿病大鼠和 Zucker 肥胖大鼠所特有的血浆葡萄糖和脂质异常。