ElGamal Heba, Munusamy Shankar
College of Pharmacy, Qatar University, P.O. Box 2713, Doha, Qatar.
Protein Pept Lett. 2017;24(1):71-77. doi: 10.2174/0929866523666161128153548.
Diabetic nephropathy (DN) is one of the most serious microvascular complications of diabetes mellitus and the leading cause of end stage renal disease. One of the key pathways activated in DN is the polyol pathway, in which glucose is converted to sorbitol (a relatively nonmetabolizable sugar) by the enzyme aldose reductase (AR). Shunting of glucose into this pathway causes disruption to glucose metabolism and subsequently damages the tissues via increased oxidative stress, protein kinase c activation and production of advanced glycation end products (AGE) in the kidney. This review aims to provide a comprehensive overview of the AR enzyme structure, substrate specificity and topology in normal physiology; to elaborate on the deleterious effects of AR activation in DN; and to summarize the potential therapeutic benefits and major challenges associated with AR inhibition in patients with DN.
糖尿病肾病(DN)是糖尿病最严重的微血管并发症之一,也是终末期肾病的主要原因。在糖尿病肾病中被激活的关键途径之一是多元醇途径,在该途径中,葡萄糖被醛糖还原酶(AR)转化为山梨醇(一种相对不可代谢的糖)。葡萄糖进入该途径会导致葡萄糖代谢紊乱,随后通过增加氧化应激、蛋白激酶c激活以及在肾脏中产生晚期糖基化终产物(AGE)来损害组织。本综述旨在全面概述醛糖还原酶在正常生理中的酶结构、底物特异性和拓扑结构;阐述醛糖还原酶激活在糖尿病肾病中的有害影响;并总结醛糖还原酶抑制对糖尿病肾病患者的潜在治疗益处和主要挑战。