Morsy Mohamed A, Heeba Gehan H, Mahmoud Magda E
Department of Pharmacology, Faculty of Medicine, Minia University, 61511 El-Minia, Egypt.
Department of Pharmacology and Toxicology, Faculty of Pharmacy, Minia University, 61511 El-Minia, Egypt.
Eur J Pharmacol. 2015 Mar 5;750:90-7. doi: 10.1016/j.ejphar.2015.01.027. Epub 2015 Jan 24.
Diabetic nephropathy becomes the single most frequent cause of end-stage renal disease. The present study aimed therefore to investigate possible protective effect of eprosartan, an angiotensin II type 1 receptor blocker, on high-fat diet/streptozotocin-induced early diabetic nephropathy in rats and various mechanisms underlie this effect. Male Wistar rats with type 2 diabetes induced by high-fat diet/streptozotocin were treated with eprosartan at the dose levels of 30 and 60mg/kg daily for 5 weeks. Eprosartan induced a nephroprotective effect as evident by the significant decrease in serum creatinine, urea, total cholesterol, triglycerides and glucose levels, urinary albumin excretion and kidney index as well as renal levels of malondialdehyde and nitric oxide products (nitrite/nitrate), in addition to angiotensin II, inducible nitric oxide synthase, transforming growth factor-β1 and collagen IV expressions with a concurrent increase in renal levels of reduced glutathione and catalase activity compared to diabetic untreated rats. Histopathological examination confirmed the renoprotective effect of eprosartan. In conclusion, eprosartan protects rats against high-fat diet/streptozotocin-induced early diabetic nephropathy possibly, in part, through its antioxidant effect as well as by abrogating the overexpression of angiotensin II, inducible nitric oxide synthase, transforming growth factor-β1 and collagen IV.
糖尿病肾病成为终末期肾病最常见的单一病因。因此,本研究旨在探讨血管紧张素II 1型受体阻滞剂依普罗沙坦对高脂饮食/链脲佐菌素诱导的大鼠早期糖尿病肾病可能的保护作用及其相关机制。将高脂饮食/链脲佐菌素诱导的2型糖尿病雄性Wistar大鼠,每日分别给予30mg/kg和60mg/kg剂量的依普罗沙坦治疗5周。依普罗沙坦显示出肾脏保护作用,表现为血清肌酐、尿素、总胆固醇、甘油三酯和血糖水平、尿白蛋白排泄量、肾脏指数以及肾脏丙二醛和一氧化氮产物(亚硝酸盐/硝酸盐)水平显著降低,此外还有血管紧张素II、诱导型一氧化氮合酶、转化生长因子-β1和IV型胶原表达降低,同时与未治疗的糖尿病大鼠相比,肾脏还原型谷胱甘肽水平升高和过氧化氢酶活性增强。组织病理学检查证实了依普罗沙坦的肾脏保护作用。总之,依普罗沙坦可能部分通过其抗氧化作用以及消除血管紧张素II、诱导型一氧化氮合酶、转化生长因子-β1和IV型胶原的过表达,保护大鼠免受高脂饮食/链脲佐菌素诱导的早期糖尿病肾病。