Exploration on the mechanism of Radix Astragali-Caulis Spatholobi by Qi-invigorating and blood-activating combination for the treatment of atherosclerosis based on network pharmacology

Haiou Lv, Chencun Huang, Ying-Jun He, Hong-Jie Liao, Tingting Zhao, Suo-yi Huang
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Abstract

The objective of this study was to investigate the main active ingredients, potential targets, and possible mechanisms of action of the combination of Radix Astragali and Caulis Spatholobi for the treatment of atherosclerosis using network pharmacology. The study aimed to provide a reference basis for the development of new formulations and clinical use of Chinese medicine. The main components of Radix Astragali and Caulis Spatholobi were obtained from the TCMSP, BATMAN-TCM database, and literature reports. The targets corresponding to the main components were imported into the Uniprot database to standardize the names, and target information was supplemented with the Swiss Target Prediction database. Disease-related targets were obtained from DrugBank, OMIM, CTD, GeneCards, and DisGeNET online databases. Venn tools were used to obtain the potential targets of Radix Astragali and Caulis Spatholobi for the treatment of AS. The intersecting genes were imported into the STRING 11.5 database to construct protein-protein interaction network maps and analyze their interactions. Cytoscape 3.7.1 software was used to mine their core targets. GO function and KEGG signaling pathway enrichment analysis were performed using the DAVID v2023q1 database. The results were imported into the “Bioinformatics Cloud Platform” to generate enrichment bubble maps. Finally, the “component-target-pathway” diagram was constructed using Cytoscape 3.7.1 software. The study found that 78 major active ingredients and 527 potential targets were obtained from Radix Astragali and Caulis Spatholobi . The main active components of the two in combination for the treatment of AS are quercetin, stigmasterol, kaempferol, luteolin, formononetin, etc. The key targets involve CDKN1A, E2F1, CDK4, CDK2, CDK1, RB1, TP53, CDKN1B, IL6, JUN, etc. The main pathways involved the AGE-RAGE signaling pathway in diabetic complications, cancer pathway, etc. The biological processes involved include positive regulation of gene expression, negative regulation of apoptotic process, etc. The study initially verified the feasibility of the combination of Radix Astragali - Caulis Spatholobi by Qi-invigorating (promoting human metabolic activity) and blood-activating for the treatment of AS. It demonstrated that the combination of Chinese medicine has multi-level, multi-target, and multi-pathway mechanisms of action to treat the disease, providing a reference basis for the development and utilization of new drugs.
基于网络药理学的黄芪-鸡血藤联合益气活血治疗动脉粥样硬化的作用机制探讨
本研究的目的是利用网络药理学研究黄芪与鸡血藤联合治疗动脉粥样硬化的主要有效成分、潜在靶点和可能的作用机制。本研究旨在为中药新剂型的开发和临床应用提供参考依据。黄芪和鸡血藤的主要成分来源于tcm数据库、BATMAN-TCM数据库和文献报道。将主要部件对应的靶材导入Uniprot数据库进行标准化命名,并用瑞士靶材预测数据库补充靶材信息。从DrugBank、OMIM、CTD、GeneCards和DisGeNET在线数据库获得疾病相关靶点。利用Venn工具获得黄芪和鸡血藤治疗AS的潜在靶点。将交叉基因导入STRING 11.5数据库,构建蛋白-蛋白相互作用网络图谱并分析其相互作用。利用Cytoscape 3.7.1软件挖掘其核心靶点。使用DAVID v2023q1数据库进行GO功能和KEGG信号通路富集分析。结果导入“生物信息学云平台”生成富集气泡图。最后利用Cytoscape 3.7.1软件构建“组件-目标-通路”图。研究发现,从黄芪和鸡血藤中分离得到78种主要有效成分和527种潜在靶点。两者联合治疗AS的主要有效成分为槲皮素、豆甾醇、山奈酚、木犀草素、刺芒柄花素等。关键靶点包括CDKN1A、E2F1、CDK4、CDK2、CDK1、RB1、TP53、CDKN1B、IL6、JUN等。主要通路包括糖尿病并发症中的AGE-RAGE信号通路、肿瘤通路等。所涉及的生物学过程包括基因表达的正向调控、细胞凋亡过程的负向调控等。本研究初步验证了黄芪-鸡血藤联合益气活血治疗AS的可行性。说明中药结合治疗该病具有多层次、多靶点、多途径的作用机制,为新药的开发利用提供参考依据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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