Molecular Mechanisms of Diabetic Retinopathy: Potential Therapeutic Targets

被引:57
|
作者
Coucha, Maha [1 ,2 ,3 ]
Elshaer, Sally L. [1 ,2 ,3 ]
Eldahshan, Wael S. [1 ,2 ,3 ]
Mysona, Barbara A. [1 ,2 ,3 ]
El-Remessy, Azza B. [1 ,2 ,3 ]
机构
[1] Univ Georgia, Program Clin & Expt Therapeut, Dept Clin Pharm, Augusta, GA 30912 USA
[2] Georgia Regents Univ, Culver Vis Discovery Inst, Augusta, GA 30912 USA
[3] Charlie Norwood VA Med Ctr, Res Serv, Augusta, GA 30912 USA
关键词
Diabetic Retinopathy; Endoplasmic Reticulum-stress; Nicotinamide Adenine; Dinucleotide Phosphate Oxidase; Inflammation; Oxidative Stress; Peroxynitrite; Therapeutics;
D O I
10.4103/0974-9233.154386
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
Diabetic retinopathy (DR) is the leading cause of blindness in working-age adults in United States. Research indicates an association between oxidative stress and the development of diabetes complications. However, clinical trials with general antioxidants have failed to prove effective in diabetic patients. Mounting evidence from experimental studies that continue to elucidate the damaging effects of oxidative stress and inflammation in both vascular and neural retina suggest its critical role in the pathogenesis of DR. This review will outline the current management of DR as well as present potential experimental therapeutic interventions, focusing on molecules that link oxidative stress to inflammation to provide potential therapeutic targets for treatment or prevention of DR. Understanding the biochemical changes and the molecular events under diabetic conditions could provide new effective therapeutic tools to combat the disease.
引用
收藏
页码:135 / 144
页数:10
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