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Local Delivery of Angiotensin II Receptor Blockers into the Kidney Passively Attenuates Inflammatory Reactions during the Early Phases of Streptozotocin-induced Diabetic Nephropathy through Inhibition of Calpain Activity

机译:血管紧张素II受体阻滞剂向肾脏的局部递送通过抑制钙蛋白酶的活性,在链脲佐菌素诱发的糖尿病性肾病的早期阶段被动地减弱了炎症反应。

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Background/Aims: Inhibition of the renin-angiotensin-al-dosterone system plays a pivotal role in the prevention and treatment of diabetic nephropathy. Angiotensin II receptor blockers (ARB) exert a renoprotective effect and attenuate the progression of diabetic nephropathy. However, the underlying cellular and molecular mechanisms in the kidney remain to be elucidated. The present study was undertaken to focus on the effect of local angiotensin II type 1 receptor blockade on the inflammatory reaction during the early stages of diabetic nephropathy. Methods and Results: Local ARB treatment significantly reduced urinary protein excretion and serum blood urea nitrogen levels in streptozotocin-induced diabetic nephropathy. In addition, this treatment attenuated monocyte/macrophage infiltration into the glomeruli and the enhanced glomerular expression of endo-thelial nitric oxide synthase at both the mRNA and protein levels. Immunohistochemical study revealed activation of nuclear factor (NF)-kappaB, as shown by an increase in the expression of the p65 subunit of NF-kappaB and its translocation from the cytoplasm to the nucleus in both tubular epithelial and glomerular cells of the diabetic kidney. Local ARB treatment induced an apparent reduction in p65 nuclear localization and intensity of staining. To search for a common and fundamental candidate that influences endothelial cell function and vascular inflammation, we examined glomerular calpain activity in diabetic rats with or without ARB treatment. Glomerular expression of 145/150-kDa spectrin breakdown products, a specific product of calpain activation, was dramatically increased in diabetic animals while the protein expression reverted to a normal level after ARB treatment. Conclusion: Our findings provide a conceptual basis for the development of therapeuticstrategiesaiming at local inhibition of the renin-angiotensin system to prevent the progression Of diabetic nephropathy.
机译:背景/目的:抑制肾素-血管紧张素-醛固酮系统在糖尿病肾病的预防和治疗中起关键作用。血管紧张素II受体阻滞剂(ARB)发挥肾脏保护作用,并减弱糖尿病性肾病的进展。但是,肾脏中潜在的细胞和分子机制仍有待阐明。进行本研究以集中于糖尿病性肾病早期阶段局部血管紧张素II 1型受体阻断对炎性反应的影响。方法和结果:局部ARB治疗可显着降低链脲佐菌素诱发的糖尿病肾病中尿蛋白排泄和血清尿素氮水平。此外,这种治疗减弱了单核细胞/巨噬细胞向肾小球的浸润,并在mRNA和蛋白质水平上增强了内皮型一氧化氮合酶的肾小球表达。免疫组织化学研究显示核因子(NF)-kappaB的激活,如糖尿病肾小管上皮和肾小球细胞中NF-kappaB p65亚基的表达增加以及其从细胞质向细胞核的转运所表明的。局部ARB处理引起p65核定位和染色强度的明显降低。为了寻找影响内皮细胞功能和血管炎症的常见且基本的候选药物,我们检查了接受或不接受ARB治疗的糖尿病大鼠的肾小球钙蛋白酶活性。在糖尿病动物中,145 / 150-kDa血影蛋白分解产物(钙蛋白酶激活的特定产物)的肾小球表达显着增加,而蛋白表达在ARB治疗后恢复到正常水平。结论:我们的发现为局部抑制肾素-血管紧张素系统以预防糖尿病性肾病发展的治疗策略的发展提供了理论基础。

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