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首页> 外文期刊>Antioxidants and redox signalling >NADPH oxidases in the kidney.
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NADPH oxidases in the kidney.

机译:肾脏中的NADPH氧化酶。

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摘要

NADPH oxidases have a distinct cellular localization in the kidney. Reactive oxygen species (ROS) are produced in the kidney by fibroblasts, endothelial cells (EC), vascular smooth muscle cells (VSMC), mesangial cells (MCs), tubular cells, and podocyte cells. All components of the phagocytic NADPH oxidase, as well as the Nox-1 and -4, are expressed in the kidney, with a prominent expression in renal vessels, glomeruli, and podocytes, and cells of the thick ascending limb of the loop of Henle (TAL), macula densa, distal tubules, collecting ducts, and cortical interstitial fibroblasts. NADPH oxidase activity is upregulated by prolonged infusion of angiotensin II (Ang II) or a high salt diet. Since these are major factors underlying the development of hypertension, renal NADPH oxidase may have an important pathophysiological role. Indeed, recent studies with small interference RNAs (siRNAs) targeted to p22( phox ) implicate p22( phox ) in Ang II-induced activation of renal NADPH oxidase and the development of oxidative stress and hypertension, while studies with apocynin implicate activation of p47( phox ) in the development of nephropathy in a rat model of type 1 diabetes mellitus (DM). Experimental studies of the distribution, signaling, and function of NADPH oxidases in the kidney are described.
机译:NADPH氧化酶在肾脏中具有独特的细胞定位。肾中的活性氧(ROS)由成纤维细胞,内皮细胞(EC),血管平滑肌细胞(VSMC),肾小球系膜细胞(MCs),肾小管细胞和足细胞产生。吞噬NADPH氧化酶的所有成分以及Nox-1和-4在肾脏中表达,在肾血管,肾小球和足细胞以及Henle the厚的上升肢体细胞中有突出表达(TAL),黄斑窝,远端小管,收集管和皮质间质成纤维细胞。长期输注血管紧张素II(Ang II)或高盐饮食会导致NADPH氧化酶活性上调。由于这些是导致高血压发展的主要因素,因此肾脏NADPH氧化酶可能具有重要的病理生理作用。确实,最近针对p22(phox)的小干扰RNA(siRNA)的研究暗示p22(phox)参与Ang II诱导的肾NADPH氧化酶的活化以及氧化应激和高血压的发展,而载有阿朴西宁的研究则暗示p47( phox)在1型糖尿病(DM)大鼠模型中发展为肾病。描述了NADPH氧化酶在肾脏中的分布,信号传导和功能的实验研究。

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