Jha Jay C, Banal Claudine, Chow Bryna S M, Cooper Mark E, Jandeleit-Dahm Karin
1 Diabetic Complications Division, JDRF Danielle Alberti Memorial Centre for Diabetic Complications, Baker IDI Heart and Diabetes Institute , Melbourne, Australia .
2 Department of Medicine, Monash University , Melbourne, Australia .
Antioxid Redox Signal. 2016 Oct 20;25(12):657-684. doi: 10.1089/ars.2016.6664. Epub 2016 Apr 1.
Intrarenal oxidative stress plays a critical role in the initiation and progression of diabetic kidney disease (DKD). Enhanced oxidative stress results from overproduction of reactive oxygen species (ROS) in the context of concomitant, insufficient antioxidant pathways. Renal ROS production in diabetes is predominantly mediated by various NADPH oxidases (NOXs), but a defective antioxidant system as well as mitochondrial dysfunction may also contribute. Recent Advances: Effective agents targeting the source of ROS generation hold the promise to rescue the kidney from oxidative damage and prevent subsequent progression of DKD. Critical Issues and Future Directions: In the present review, we summarize and critically analyze molecular and cellular mechanisms that have been demonstrated to be involved in NOX-induced renal injury in diabetes, with particular focus on the role of increased glomerular injury, the development of albuminuria, and tubulointerstitial fibrosis, as well as mitochondrial dysfunction. Furthermore, novel agents targeting NOX isoforms are discussed. Antioxid. Redox Signal. 25, 657-684.
肾内氧化应激在糖尿病肾病(DKD)的发生和发展中起关键作用。在抗氧化途径不足的同时,活性氧(ROS)的过度产生导致氧化应激增强。糖尿病中肾脏ROS的产生主要由各种烟酰胺腺嘌呤二核苷酸磷酸氧化酶(NOXs)介导,但抗氧化系统缺陷以及线粒体功能障碍也可能起作用。最新进展:针对ROS产生源的有效药物有望使肾脏免受氧化损伤,并预防DKD的后续进展。关键问题和未来方向:在本综述中,我们总结并批判性地分析了已被证明参与糖尿病中NOX诱导的肾损伤的分子和细胞机制,特别关注肾小球损伤增加、蛋白尿的发展和肾小管间质纤维化以及线粒体功能障碍的作用。此外,还讨论了针对NOX亚型的新型药物。《抗氧化与氧化还原信号》25卷,657 - 684页。