醛糖还原酶抑制剂

M. Oka, N. Kato
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引用次数: 84

摘要

醛糖还原酶([EC1.1.1.21]: AR)在多元醇代谢途径的第一步,以NADPH为辅酶催化葡萄糖还原为山梨醇。高血糖个体中该通路的过度活跃与糖尿病并发症的发生或进展密切相关。因此,AR抑制剂被认为是治疗糖尿病并发症的可能药物治疗药物。一种AR抑制剂已经在日本上市,而一些有效的抑制剂正在临床试验中。本文综述了AR的生理作用、AR抑制剂的化学结构、AR抑制剂与AR的x射线相互作用,以及AR抑制剂的以下功效:AR的体外活性、AR与醛还原酶的体外选择性、它们的体内药理作用以及它们在临床试验中的有效性。讨论了未来AR抑制剂的设计方向。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Aldose Reductase Inhibitors
Aldose reductase ([EC1.1.1.21]: AR) acts on the first step of the polyol metabolic pathway to catalyze the reduction of glucose to sorbitol with NADPH as a coenzyme. Hyperactivity of the pathway in individuals with high blood glucose level is closely related to the onset or progression of diabetic complications. AR inhibitors have therefore been noted as possible pharmacotherapeutic agents for the treatment of diabetic complications. One AR inhibitor has been on the market in Japan, while some potent inhibitors are in clinical trials. Reviewed are the physiological roles of AR, the chemical structures of AR inhibitors, interactions of AR inhibitors with AR using X-ray studies, and the following potencies of AR inhibitors: in vitro activities for AR, in vitro selectivities between AR and aldehyde reductase, their pharmacological effects in vivo, and their effectiveness in clinical trials. Also discussed are directions for the design of future AR inhibitors.
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