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Epithelial-to-Mesenchymal Transdifferentiation of Renal Tubular Epithelial Cell Mediated by Oxidative Stress and Intervention Effect of Probucol in Diabetic Nephropathy Rats

机译:糖尿病肾病大鼠氧化应激介导的肾小管上皮细胞上皮间质转分化及普罗布考的干预作用

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Objective: To elucidate the relationship of oxidative stress and specificity protein 1 (Sp1) in the process of epithelial-to-mesenchymal transdifferentiation (EMT) and also to investigate the molecular mechanism of protective effect of probucol on the pathogenesis of diabetic kidney disease (DKD). Methods: Thirty male Sprague–Dawley (SD) rats were randomly divided into control group, diabetic group, and diabetic group under probucol therapy (n = 10 per group). The biochemical indicators including 24-h urinary total protein (24-h UTP) excretion, blood glucose (BG), lipids [triglycerides (TGs), total cholesterol (TC)], serum creatinine (Scr), creatinine clearance rate (Ccr), kidney tissue malondialdehyde (MDA) level, and glutathione peroxidase (GSH-Px) activity were assessed in all groups. The renal pathological changes were evaluated by hematoxylin and eosin (HE) and Masson staining. The protein expression of Sp1, α-smooth muscle actin (α-SMA), and E-cadherin was also measured and analyzed by immunohistochemistry and Western blotting. Results: Compared with the control group, the BG, TC, Scr, 24-h UTP, and MDA level of renal tissue increased significantly and the Ccr reduced in the rats of diabetic group (all p α-SMA in renal tissue were up-regulated (p p p Conclusions: Oxidative stress may play an important role in the EMT process of tubular epithelial cells. Probucol could ameliorate renal disease progression in this model of diabetic nephropathy, which might be due to an antioxidant action, down-regulation of Sp1 protein expression, and inhibition of renal tubular EMT.
机译:目的:阐明氧化应激与特异性蛋白1(Sp1)在上皮间质转分化(EMT)过程中的关系,并探讨普罗布考对糖尿病肾病(DKD)发病机理的分子机制。 )。方法:将30只雄性Sprague-Dawley(SD)大鼠在普罗布考治疗下随机分为对照组,糖尿病组和糖尿病组(每组10只)。生化指标包括24小时尿总蛋白(24小时UTP)排泄,血糖(BG),脂质[甘油三酸酯(TGs),总胆固醇(TC)],血清肌酐(Scr),肌酐清除率(Ccr) ,肾脏组织中的丙二醛(MDA)水平和谷胱甘肽过氧化物酶(GSH-Px)活性均在所有组中进行了评估。通过苏木精和曙红(HE)和Masson染色评估肾脏病理变化。还通过免疫组织化学和蛋白质印迹法测量和分析了Sp1,α-平滑肌肌动蛋白(α-SMA)和E-钙粘蛋白的蛋白表达。结果:与对照组相比,糖尿病组大鼠肾组织的BG,TC,Scr,24h UTP和MDA水平显着升高,Ccr降低(肾组织中所有pα-SMA均升高- (ppp结论:氧化应激可能在肾小管上皮细胞的EMT过程中起重要作用。普罗布考可以改善这种糖尿病肾病模型中的肾脏疾病进展,这可能是由于抗氧化作用,Sp1蛋白表达下调所致,并抑制肾小管EMT。

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