硅学分析揭示了蒲公英萜醇(Coccinia indica)和淫羊藿内酯-1(Withania coagulans)抑制α-淀粉酶的潜力:一种控制餐后高血糖诱发的内皮功能障碍和心血管事件的可能方法。

In silico pharmacology Pub Date : 2024-09-09 eCollection Date: 2024-01-01 DOI:10.1007/s40203-024-00257-6
Lokesh Ravi, Venkatesh Sadhana, Pratishtha Jain, Shree Kumari Godidhar Raghuram, Mohanasrinivasan Vaithilingam, Reji Manjunathan, Ajith Kumar Krishnan, Mookkandi Palsamy Kesavan
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引用次数: 0

摘要

餐后高血糖症(PPG)会加剧糖尿病患者以及健康人的内皮功能障碍并损害血管功能。虽然有合成药物可以调节餐后高血糖,但这些药物对胃肠道的严重副作用促使人们寻找替代疗法。最近,一些植物化学物质引起了人们的注意,因为它们对α-淀粉酶有抑制作用,可以控制糖尿病。本研究的目的是调查和鉴定 C. indica 和 W. coagulans 中潜在的α-淀粉酶抑制剂。本研究还旨在了解植物抗糖尿病活性的可能作用机制之一。共有 36 种植物化学配体被用于蛋白质配体对接分析。在这些植物化学配体中,蒲公英萜醇(Taraxerol)和环氧丹皮酚内酯(Epoxywithanolide-I)的结合自由能分别为-10.2 kcal/mol和-11.9 kcal/mol,高于阿卡波糖(acarbose)的-8.6 kcal/mol。这些分子与α-淀粉酶蛋白进行了持续时间为 150 ns 的分子动力学模拟(MDS)分析。在这三种复合物中,Taraxerol 和 Epoxywithanolide-I 复合物显示出作为目标蛋白质抑制剂的强大潜力。通过均方根偏差(RMSD)、残基波动、势能、回旋半径和溶剂接触表面积分析,对 MDS 结果进行了分析。蒲公英萜醇的势能明显较低,为-1,924,605.25 kJ/mol,而 Epoxywithanolide-I 的势能为-1,964,113.3 kJ/mol。RMSD 图显示,Epoxywithanolide-I 的稳定性远高于其他 MDS 复合物。可药用性和毒性研究表明,测试配体作为类药物分子具有很强的潜力。研究结果得出结论,籼稻中的蒲公英萜醇(Taraxerol of C. indica)和W. coagulans中的环氧花青素-I(Epoxywithanolide-I)是α-淀粉酶的强力抑制剂,这也是这些植物据报道具有抗糖尿病活性的可能作用机制之一。需要进一步的体外分析来证明观察到的结果。
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In silico analysis reveals α-amylase inhibitory potential of Taraxerol (Coccinia indica) and Epoxywithanolide-1 (Withania coagulans): a possible way to control postprandial hyperglycemia-induced endothelial dysfunction and cardiovascular events.

Postprandial hyperglycemia (PPG) exacerbates endothelial dysfunction and impairs vascular function in diabetes as well in healthy people. Though synthetic drugs are available to regulate PPG, the severe gastrointestinal side effects of those medications have prompted the search for alternative treatments. Recently, some phytochemicals captured the attention because of their inhibitory effects on α-amylase to control diabetes. The aim of this study was to investigate and identify potential alpha-amylase inhibitors in C. indica and W. coagulans. This study also aims to understand one of the possible mechanisms of action of plants for their anti-diabetic activity. A total of 36 phytochemical ligands were subjected for protein-ligand docking analysis. Among the phytochemicals, Taraxerol and Epoxywithanolide-I demonstrated significant binding free energy of - 10.2 kcal/mol and - 11.9 kcal/mol respectively, which was higher than the reference acarbose with - 8.6 kcal/mol. These molecules were subjected for molecular dynamics simulation (MDS) analysis with alpha-amylase protein for a duration of 150 ns. Among the three complexes, Taraxerol and Epoxywithanolide-I complexes demonstrates strong potential as inhibitors of the target protein. MDS results were analyzed via root mean square deviation (RMSD), fluctuation of residues, potential energy, radii of gyration and solvent access surface area analysis. Taraxerol demonstrated a significantly low potential energy of - 1,924,605.25 kJ/mol, and Epoxywithanolide-I demonstrated - 1,964,113.3 kJ/mol of potential energy. RMSD plot shows that Epoxywithanolide-I has much higher stability than the other MDS complexes. Drugability and toxicity studies show that the test ligands are demonstrating strong potential as drug like molecules. The results of the study conclude that, Taraxerol of C. indica and Epoxywithanolide-I of W. coagulans are strong inhibitors of alpha-amylase enzyme and that, this is one of the possible mechanisms of action of the plants for their reported anti-diabetic activities. Further in-vitro analysis is in demand to prove the observed results.

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