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来自[具体来源未提及]的阿朱诺酸与冠状动脉疾病靶点APOE4的分子对接分析。

Molecular docking analysis of arjunolic acid from with a coronary artery disease target APOE4.

作者信息

Hazarika Lima, Sen Supriyo, Doshi Jitesh

机构信息

Department of Biosciences, Assam Don Bosco University, Sonapur, 782402, Assam, India.

BioInsight Solutions Private Limited, Kharghar, Navi Mumbai,410210, Maharashtra, India.

出版信息

Bioinformation. 2021 Nov 30;17(11):949-958. doi: 10.6026/97320630017949. eCollection 2021.

DOI:10.6026/97320630017949
PMID:35655909
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9148589/
Abstract

Apo lipoprotein-E (APOE) encoded by APOE gene, is a plasma glycoprotein of 34.15 kDa and has a significant genetic association in coronary artery disease (CAD) progression. The silent epidemic of different cardiovascular diseases including CAD challenges novel therapeutic alternatives to prevent to treat chronic conditions of the disease and its associated complications. It is believed that natural phyto compounds and extracts have been a potential source of treating health conditions and have been practiced since several decades. The aim of the study is to identify phyto compounds having significant cardio protective activity targeting APOE4. Since protein-ligand interactions play a leading role in structure-based drug design, with the help of molecular docking, we selected 20 phyto chemicals present in different plants and investigated their binding affinity against targeted APOE isoforms. Among all selected phytoc ompounds, arjunolic acid, from Terminalia arjuna plant was found as promising candidate for developing therapeutic against APOE4 activated CAD. Findings from the present work could be further studied for clinical evaluations on human to adopt strategies and reduce the prevalence and mortality. Arjunolic acid derivatives can be used as a source of new medication or development of novel compounds in the treatment of CAD.

摘要

载脂蛋白E(APOE)由APOE基因编码,是一种34.15 kDa的血浆糖蛋白,在冠状动脉疾病(CAD)进展中具有显著的遗传关联。包括CAD在内的不同心血管疾病的悄然流行对预防和治疗该疾病的慢性病及其相关并发症的新型治疗选择提出了挑战。人们认为,天然植物化合物和提取物一直是治疗健康状况的潜在来源,并且已经应用了几十年。本研究的目的是鉴定针对APOE4具有显著心脏保护活性的植物化合物。由于蛋白质-配体相互作用在基于结构的药物设计中起主导作用,借助分子对接,我们选择了不同植物中存在的20种植物化学物质,并研究了它们对靶向APOE异构体的结合亲和力。在所有选定的植物化合物中,来自诃子植物的阿朱诺酸被发现是开发针对APOE4激活的CAD治疗药物的有希望的候选物。本研究结果可进一步进行人体临床评估,以采取策略并降低患病率和死亡率。阿朱诺酸衍生物可作为治疗CAD的新药来源或新型化合物的开发。