Diabetes and Kidney Disease: Role of Oxidative Stress

被引:571
作者
Jha, Jay C. [1 ]
Banal, Claudine [1 ]
Chow, Bryna S. M. [1 ]
Cooper, Mark E. [1 ,2 ]
Jandeleit-Dahm, Karin [1 ,2 ]
机构
[1] Baker IDI Heart & Diabet Inst, Diabet Complicat Div, JDRF Danielle Alberti Mem Ctr Diabet Complicat, POB 6492 St Kilda Rd, Melbourne, Vic 8008, Australia
[2] Monash Univ, Dept Med, Melbourne, Vic, Australia
基金
英国医学研究理事会;
关键词
reactive oxygen species; NADPH-oxidases; diabetic nephropathy; albuminuria; ENDOTHELIAL NITRIC-OXIDE; GROWTH-FACTOR-BETA; PHAGOCYTE NADPH OXIDASE; KINASE-C-BETA; GLOMERULAR MESANGIAL CELLS; NF-KAPPA-B; EPITHELIAL-MESENCHYMAL TRANSITION; CHRONIC GRANULOMATOUS-DISEASE; OXYGEN SPECIES GENERATION; THICK ASCENDING LIMB;
D O I
10.1089/ars.2016.6664
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Significance: 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.
引用
收藏
页码:657 / 684
页数:28
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