吲哚-3-羧醛衍生物对醛糖还原酶活性的影响

Orçun Erdem Kurşun, S. Süzen, Ö. Yildirim
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引用次数: 2

摘要

在糖尿病患者中,醛糖还原酶(AR, EC 1.1.1.21)在晶状体、肾脏和神经组织中的活性显著增加。主要在眼部和神经组织中,山梨醇水平的升高与糖尿病并发症有关,如视网膜病变、肾病、神经性病变、白内障的形成以及活性氧含量的增加引起的组织损伤。最近,有许多研究表明该酶家族与癌症之间的关系。醛糖还原酶对这一途径非常重要,因此也成为药物设计的潜在靶点。大量醛糖还原酶抑制剂(ARIs)被用于预防或延缓这些糖尿病并发症和癌症。然而,有效的ARIs对糖尿病并发症的益处仍在研究中。本研究从牛晶体中部分纯化醛糖还原酶,并采用动力学方法考察了16种吲哚-3-羧基醛衍生物对醛糖还原酶活性的抑制作用。结果表明,N′-[(5-溴- 1h -吲哚-3-基)甲基]吡啶-4-碳肼对AR的抑制活性最高。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
ALTERATIONS OF ALDOSE REDUCTASE ACTIVITY BY INDOLE-3-CARBOXALDEHYDE DERIVATIVES
In diabetic conditions, aldose reductase (AR, EC 1.1.1.21) activity is significantly increased in lens, kidney and nerve tissues. Mainly in ocular and neural tissues increased levels of sorbitol is associated with diabetic complications such as retinopathy, nephropathy, neuropahty, cataract formation and also tissue damage via increased reactive oxygen speices. Recently, there are many studies that show the relationship between this enzyme family and cancer. Aldose reductase is important for the pathway and in turn has been a potential target for drug design. Great number of aldose reductase inhibitors (ARIs) are used for prevention or delay of these diabetic complications and cancer. However, effective ARIs which has benefits in diabetic complications are still under investigation. In this study aldose reductase was partially purified from bovine lens and the inhibitory effects of 16 different indol-3-carboxyaldehydederivatives on aldose reductase enzyme activities were examined by kinetic assays. These results suggested that N'-[(5-bromo-1H-indol-3-yl)methylidene]pyridine-4-carbohydrazide showed that the highest inhibitory activity on AR.
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