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印度牛弭草变种柔毛牛弭草根提取物(一种醛糖还原酶抑制剂)对多元醇途径活性的抑制作用:一项计算机模拟和体外研究

Repression of Polyol Pathway Activity by Hemidesmus indicus var. pubescens R.Br. Linn Root Extract, an Aldose Reductase Inhibitor: An In Silico and Ex Vivo Study.

作者信息

Haroon Hajira Banu, Perumalsamy Vijaybhanu, Nair Gouri, Anand Dhanusha Koppal, Kolli Rajitha, Monichen Joel, Prabha Kanchan

机构信息

Department of Pharmacology, Faculty of Pharmacy, M S Ramaiah University of Applied Sciences, Gnanagangothri Campus, New BEL Road, Bengaluru, Karnataka, 560054, India.

Department of Pharmaceutical Chemistry, Faculty of Pharmacy, M S Ramaiah University of Applied Sciences, Gnanagangothri Campus, New BEL Road, Bengaluru, Karnataka, 560054, India.

出版信息

Nat Prod Bioprospect. 2021 Jun;11(3):315-324. doi: 10.1007/s13659-020-00290-w. Epub 2020 Dec 7.

Abstract

Development of diabetic cataract is mainly associated with the accumulation of sorbitol via the polyol pathway through the action of Aldose reductase (AR). Hence, AR inhibitors are considered as potential agents in the management of diabetic cataract. This study explored the AR inhibition potential of Hemidesmus indicus var. pubescens root extract by in silico and ex vivo methods. Molecular docking studies (Auto Dock tool) between β-sitosterol, hemidesminine, hemidesmin-1, hemidesmin-2, and AR showed that β-sitosterol (- 10.2 kcal/mol) and hemidesmin-2 (- 8.07 kcal/mol) had the strongest affinity to AR enzyme. Ex vivo studies were performed by incubating isolated goat lenses in artificial aqueous humor using galactose (55 mM) as cataract inducing agent at room temperature (pH 7.8) for 72 h. After treatment with Vitamin E acetate - 100 µg/mL (standard) and test extract (500 and 1000 µg/mL) separately, the estimation of biochemical markers showed inhibition of lens AR activity and decreased sorbitol levels. Additionally, extract also normalized the levels of antioxidant markers like SOD, CAT, GSH. Our results showed evidence that H. indicus var. pubescens root was able to prevent cataract by prevention of opacification and formation of polyols that underlines its potential as a possible therapeutic agent against diabetic complications.

摘要

糖尿病性白内障的发展主要与通过醛糖还原酶(AR)作用的多元醇途径导致的山梨醇积累有关。因此,AR抑制剂被认为是治疗糖尿病性白内障的潜在药物。本研究通过计算机模拟和体外实验方法探索了印度牛弭草根提取物的AR抑制潜力。β-谷甾醇、半枝莲碱、半枝莲碱-1、半枝莲碱-2与AR之间的分子对接研究(自动对接工具)表明,β-谷甾醇(-10.2 kcal/mol)和半枝莲碱-2(-8.07 kcal/mol)对AR酶具有最强的亲和力。体外实验是在室温(pH 7.8)下,将分离的山羊晶状体在以半乳糖(55 mM)作为白内障诱导剂的人工房水中孵育72小时。分别用维生素E醋酸酯-100 μg/mL(标准品)和测试提取物(500和1000 μg/mL)处理后,生化标志物的测定显示晶状体AR活性受到抑制,山梨醇水平降低。此外,提取物还使超氧化物歧化酶、过氧化氢酶、谷胱甘肽等抗氧化标志物的水平恢复正常。我们的结果表明,印度牛弭草根能够通过防止浑浊和多元醇的形成来预防白内障,这突出了其作为抗糖尿病并发症潜在治疗药物的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f138/8141070/1ab4cf1d178f/13659_2020_290_Fig1a_HTML.jpg

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