醛糖还原酶
多元醇途径
糖基化
糖尿病肾病
糖尿病
肾病
山梨醇
山梨醇脱氢酶
药理学
氧化应激
醛糖还原酶抑制剂
化学
医学
生物化学
足细胞
内科学
内分泌学
肾
蛋白尿
作者
Heba ElGamal,Shankar Munusamy
出处
期刊:Protein and Peptide Letters
[Bentham Science]
日期:2016-12-13
卷期号:24 (1): 71-77
被引量:11
标识
DOI:10.2174/0929866523666161128153548
摘要
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. Keywords: Diabetic nephropathy, aldose reductase, polyol pathway, protein kinase C, sorbitol, oxidative stress, advanced glycation end products.
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