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首页> 外文期刊>European Journal of Pharmacology: An International Journal >Ameliorative effect of eprosartan on high-fat diet/streptozotocin-induced early diabetic nephropathy in rats
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Ameliorative effect of eprosartan on high-fat diet/streptozotocin-induced early diabetic nephropathy in rats

机译:依普罗沙坦对高脂饮食/链脲佐菌素所致大鼠早期糖尿病肾病的改善作用

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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 60 mg/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 (nitriteitrate), in addition to angiotensin II, inducible nitric oxide synthase, transforming growth factor-beta(1) 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-beta(1) and collagen IV. (C) 2015 Elsevier B.V. All rights reserved.
机译:糖尿病肾病成为终末期肾脏疾病的最常见原因。因此,本研究旨在研究依普罗沙坦(一种血管紧张素II型受体阻滞剂)对高脂饮食/链脲佐菌素诱发的大鼠早期糖尿病肾病的可能保护作用,以及多种机制可能是该作用的雄性Wistar大鼠,由2型糖尿病引起高脂饮食/链脲佐菌素用依普罗沙坦治疗,剂量为每天30和60 mg / kg,持续5周。依普罗沙坦具有肾保护作用,其血清肌酐,尿素,总胆固醇,甘油三酯和葡萄糖水平,尿白蛋白排泄量和肾脏指数以及丙二醛和一氧化氮产物(亚硝酸盐/硝酸盐)的肾脏水平显着降低,证明了这一点。与糖尿病未治疗的大鼠相比,血管紧张素II,诱导型一氧化氮合酶,转化生长因子-β(1)和胶原蛋白IV的表达与同时降低的谷胱甘肽和过氧化氢酶活性的肾脏水平增加有关。组织病理学检查证实了依普罗沙坦的肾保护作用。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的过表达,转化生长因子-β(1)的表达,从而保护大鼠免受高脂饮食/链脲佐菌素所致的早期糖尿病肾病的侵害。和胶原蛋白IV。 (C)2015 Elsevier B.V.保留所有权利。

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