抗坏血酸降血脂的机制:硅分子对接

M. Yadav, J. Malik
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引用次数: 0

摘要

摘要:抗坏血酸又称维生素C,是均衡饮食的重要组成部分。维生素C的历史与人类坏血病的历史交织在一起,坏血病可能是第一个被确定为人类缺乏维生素C的疾病。其症状包括腹泻、全身虚弱、组织和牙龈严重出血以及疲劳。抗坏血酸是一种水溶性化学分子,对许多生物功能至关重要。抗坏血酸降脂作用的确切机制尚不清楚。为了提出抗坏血酸最可能的作用机制,我们对ATP柠檬酸裂解酶、羊毛甾醇14α-去甲基化酶、角鲨烯合成酶、Niemann Pick C1 like Protein等降脂药物靶点进行了对接计算分析。对接分析、化学相互作用以及基于物理化学的药代动力学分析表明,抗坏血酸是通过抑制角鲨烯合成酶来发挥其降脂作用的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Mechanistic Insight Hypolipidemic Potential of Ascorbic Acid: In-Silico Molecular Docking
Abstract: Ascorbic acid, also known as vitamin C, is a crucial part of a balanced diet. The history of vitamin C is intertwined with that of the human ailment scurvy, which was perhaps the first to be identified as a deficiency condition in humans. Its signs include diarrhoea, overall weakness, severe bleeding of the tissues and gums, and tiredness. Ascorbic acid is a water-soluble chemical molecule essential to numerous biological functions. The exact mechanism of action for the lipid lowering action of ascorbic acid was still not revealed. With intent to propose the most probable mechanism of action of ascorbic acid the docking based computational analysis has been performed against the lipid lowering drug targets like ATP citrate lyase enzyme, lanosterol 14α-demethylase enzyme, squalene synthase enzyme, and Niemann Pick C1 like Protein. The docking analysis, chemical interactions, followed by the physicochemical based pharmacokinetic profiling has revealed that the ascorbic acid is executing its lipid lowering action via inhibiting the squalene synthase enzyme.
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