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本文引用的文献

1
Renoprotective effects of a novel Nox1/4 inhibitor in a mouse model of Type 2 diabetes.新型 Nox1/4 抑制剂在 2 型糖尿病小鼠模型中的肾保护作用。
Clin Sci (Lond). 2013 Feb;124(3):191-202. doi: 10.1042/CS20120330.
2
Role of renal DJ-1 in the pathogenesis of hypertension associated with increased reactive oxygen species production.肾脏 DJ-1 在活性氧产物增加相关高血压发病机制中的作用。
Hypertension. 2012 Feb;59(2):446-52. doi: 10.1161/HYPERTENSIONAHA.111.185744. Epub 2012 Jan 3.
3
Angiotensin II stimulates epithelial sodium channels in the cortical collecting duct of the rat kidney.血管紧张素 II 刺激大鼠肾脏皮质集合管中的上皮钠通道。
Am J Physiol Renal Physiol. 2012 Mar 15;302(6):F679-87. doi: 10.1152/ajprenal.00368.2011. Epub 2011 Dec 14.
4
Angiotensin II increases activity of the epithelial Na+ channel (ENaC) in distal nephron additively to aldosterone.血管紧张素 II 可增强远曲小管上皮钠离子通道 (ENaC) 的活性,与醛固酮有相加作用。
J Biol Chem. 2012 Jan 2;287(1):660-671. doi: 10.1074/jbc.M111.298919. Epub 2011 Nov 15.
5
Defective nitric oxide production impairs angiotensin II-induced Na-K-ATPase regulation in spontaneously hypertensive rats.一氧化氮产生缺陷损害自发性高血压大鼠血管紧张素 II 诱导的 Na-K-ATP 酶调节。
Am J Physiol Renal Physiol. 2012 Jan 1;302(1):F47-51. doi: 10.1152/ajprenal.00270.2011. Epub 2011 Sep 7.
6
Abundance of TRPC6 protein in glomerular mesangial cells is decreased by ROS and PKC in diabetes.在糖尿病中,ROS 和 PKC 会使肾小球系膜细胞中的 TRPC6 蛋白含量减少。
Am J Physiol Cell Physiol. 2011 Aug;301(2):C304-15. doi: 10.1152/ajpcell.00014.2011. Epub 2011 Apr 27.
7
NOX isoforms and reactive oxygen species in vascular health.血管健康中的NADPH氧化酶亚型与活性氧物质
Mol Interv. 2011 Feb;11(1):27-35. doi: 10.1124/mi.11.1.5.
8
Inhibition of renal gluconeogenesis contributes to hypoglycaemic action of NADPH oxidase inhibitor, apocynin.NADPH 氧化酶抑制剂阿朴肉桂酸抑制肾糖异生,从而发挥降血糖作用。
Chem Biol Interact. 2011 Jan 15;189(1-2):119-26. doi: 10.1016/j.cbi.2010.09.033. Epub 2010 Oct 8.
9
Antiatherosclerotic and renoprotective effects of ebselen in the diabetic apolipoprotein E/GPx1-double knockout mouse.依布硒啉在糖尿病载脂蛋白 E/GPx1 双敲除小鼠中的抗动脉粥样硬化和肾保护作用。
Diabetes. 2010 Dec;59(12):3198-207. doi: 10.2337/db10-0195. Epub 2010 Sep 7.
10
Bilirubin and biliverdin protect rodents against diabetic nephropathy by downregulating NAD(P)H oxidase.胆红素和胆绿素通过下调 NAD(P)H 氧化酶来保护啮齿动物免受糖尿病肾病的侵害。
Kidney Int. 2010 Nov;78(9):905-19. doi: 10.1038/ki.2010.265. Epub 2010 Aug 4.

NADPH 氧化酶、活性氧物质与肾脏:亦敌亦友。

NADPH oxidases, reactive oxygen species, and the kidney: friend and foe.

机构信息

Kidney Research Centre, Ottawa Hospital Research Institute, University of Ottawa, Ottawa, Ontario, Canada;

出版信息

J Am Soc Nephrol. 2013 Oct;24(10):1512-8. doi: 10.1681/ASN.2012111112. Epub 2013 Aug 22.

DOI:10.1681/ASN.2012111112
PMID:23970124
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3785272/
Abstract

Reactive oxygen species (ROS) play an important role in normal cellular physiology. They regulate different biologic processes such as cell defense, hormone synthesis and signaling, activation of G protein-coupled receptors, and ion channels and kinases/phosphatases. ROS are also important regulators of transcription factors and gene expression. On the other hand, in pathologic conditions, a surplus of ROS in tissue results in oxidative stress with various injurious consequences such as inflammation and fibrosis. NADPH oxidases are one of the many sources of ROS in biologic systems, and there are seven isoforms (Nox1-5, Duox1, Duox2). Nox4 is the predominant form in the kidney, although Nox2 is also expressed. Nox4 has been implicated in the basal production of ROS in the kidney and in pathologic conditions such as diabetic nephropathy and CKD; upregulation of Nox4 may be important in renal oxidative stress and kidney injury. Although there is growing evidence indicating the involvement of NADPH oxidase in renal pathology, there is a paucity of information on the role of NADPH oxidase in the regulation of normal renal function. Here we provide an update on the role of NADPH oxidases and ROS in renal physiology and pathology.

摘要

活性氧 (ROS) 在正常细胞生理学中发挥着重要作用。它们调节着不同的生物过程,如细胞防御、激素合成和信号传递、G 蛋白偶联受体和离子通道及激酶/磷酸酶的激活。ROS 也是转录因子和基因表达的重要调节剂。另一方面,在病理条件下,组织中 ROS 的过剩会导致氧化应激,产生各种有害后果,如炎症和纤维化。NADPH 氧化酶是生物系统中 ROS 的众多来源之一,有七种同工型(Nox1-5、Duox1、Duox2)。Nox4 是肾脏中的主要形式,尽管 Nox2 也有表达。Nox4 参与了肾脏中 ROS 的基础产生以及糖尿病肾病和 CKD 等病理条件下的产生;Nox4 的上调可能在肾脏氧化应激和肾脏损伤中很重要。尽管越来越多的证据表明 NADPH 氧化酶参与了肾脏病理学,但关于 NADPH 氧化酶在调节正常肾功能中的作用的信息却很少。本文就 NADPH 氧化酶和 ROS 在肾脏生理学和病理学中的作用提供了最新进展。