[Aldose reductase inhibitors].

Journal de pharmacologie Pub Date : 1986-10-01
P Dostert, M Strolin Benedetti
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Abstract

Aldose reductase (AR) is an enzyme which catalyzes the transformation of D-glucose to sorbitol. Under non physiological conditions, like diabetes for example, the accumulation of polyols in the lens, sorbitol in particular, gives a basis to the osmotic hypothesis of cataract formation. AR inhibitors can protect against such accumulation. Oxidation of the constituents of the lens is a primary phenomenon in cataract formation, and some authors have suggested that the autoxidation of monosaccharides would originate the formation of cataract. For these authors, AR inhibitors would act by trapping the radical intermediates formed, inhibiting the denaturation of proteins in the organ and the lowering of glutathione. There classes of AR inhibitors can be distinguished: flavonoids and their related compounds, spirohydantoins--like sorbinil--and related compounds, and compounds with an acid function such as alrestatine. For each of these three classes, the authors try to establish the structure-activity relationship of the molecules. The possibility of a single site of interaction between AR and the different AR inhibitors is discussed. Differences in the inhibitory effect for a given compound between species, and for one species between tissues have been underlined.

醛糖还原酶抑制剂。
醛糖还原酶(AR)是一种催化d -葡萄糖转化为山梨醇的酶。在非生理条件下,例如糖尿病,晶状体中多元醇的积累,特别是山梨糖醇,为白内障形成的渗透性假说提供了依据。AR抑制剂可以防止这种积累。晶状体成分的氧化是白内障形成的主要现象,一些作者认为单糖的自氧化可能是白内障形成的起源。对于这些作者来说,AR抑制剂将通过捕获形成的自由基中间体,抑制器官中蛋白质的变性和谷胱甘肽的降低而起作用。AR抑制剂可分为以下几类:类黄酮及其相关化合物,螺酰胆碱(如山梨醇)及其相关化合物,以及具有酸功能的化合物,如阿莱他汀。对于这三类分子,作者试图建立分子的构效关系。讨论了AR与不同AR抑制剂之间单一位点相互作用的可能性。在物种之间的抑制作用的差异,并为一个物种之间的组织已经强调。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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