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Losartan Affects Glomerular AKT and mTOR Phosphorylation in an Experimental Model of Type 1 Diabetic Nephropathy

机译:氯沙坦影响1型糖尿病肾病实验模型的肾小球AKT和mTOR磷酸化。

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摘要

The AKT-mTOR pathway is activated in diabetic nephropathy. Renin-angiotensin system modulators exert beneficial effects on the diabetic kidney. We explored the action of losartan on AKT-mTOR phosphorylation in glomeruli and podocytes. Diabetes mellitus was induced to Sprague-Dawley rats by streptozotocin. Five months later, the rats were commenced on losartan and euthanized 2 months later. Kidneys were processed for immunofluorescence studies. Glomeruli were isolated for Western blot analysis. Diabetes increased activated forms of AKT and mTOR both in glomeruli and podocytes. In diabetic rats, losartan decreased phosphorylated/activated forms of AKT (Thr308) and mTOR (Ser2448) in glomeruli but decreased only activated mTOR in podocytes. However, in both glomeruli and podocytes of healthy animals, an inverse pattern was evident. In conclusion, a new body of evidence indicates the differential activation of AKT-mTOR in glomeruli and podocytes of healthy and diabetic animals in response to losartan.
机译:AKT-mTOR途径在糖尿病性肾病中被激活。肾素-血管紧张素系统调节剂对糖尿病肾产生有益作用。我们探索了氯沙坦对肾小球和足细胞中AKT-mTOR磷酸化的作用。链脲佐菌素对Sprague-Dawley大鼠产生糖尿病。 5个月后,大鼠开始使用氯沙坦,并在2个月后安乐死。处理肾脏进行免疫荧光研究。分离肾小球用于蛋白质印迹分析。糖尿病增加肾小球和足细胞中AKT和mTOR的活化形式。在糖尿病大鼠中,氯沙坦可降低肾小球中AKT(Thr308)和mTOR(Ser2448)的磷酸化/激活形式,而仅降低足细胞中激活的mTOR。然而,在健康动物的肾小球和足细胞中,都存在相反的模式。总之,新的证据表明,健康和糖尿病动物的肾小球和足细胞对氯沙坦的反应中,AKT-mTOR的差异激活。

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