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基于网络药理学的黄柏治疗溃疡性结肠炎机制探讨

iscussion on mechanism of Phellodendri Chinensis Cortex in treatment of ulcerative colitis based on network pharmacology

中文摘要英文摘要

目的:通过网络药理学方法探索黄柏治疗溃疡性结肠炎(Ulcerative colitis,UC)的作用机制。方法:通过BATMAN-TCM数据库筛选并获得黄柏的活性成分及其作用靶点,利用GeneCards数据库寻找UC相关疾病靶点。将黄柏活性成分的作用靶点与UC相关靶点对应,筛选交集靶点及关键活性成分。利用Cytoscape 3.8.2软件,构建黄柏活性成分与UC作用靶点网络,借助STRING平台获取蛋白相互作用网络。通过DAVID在线分析工具进行GO功能富集分析和KEGG信号通路富集分析。结果:在黄柏中筛选得到26个与UC相关的主要活性成分,关键靶点为DRD2、ESR1、NR3C1、ADRA2A和AR,KEGG富集分析结果表明其主要涉及TRP通道的炎症介质调节、鞘脂信号通路、cAMP和TNF信号通路等。结论:黄柏通过多成分、多靶点、多通路的作用方式治疗UC,为未来研究提供了新的方向。

Objective:To explore the mechanism of Phellodendri Chinensis Cortex in treatment of ulcerative colitis(UC)through network pharmacology method. Methods:The active ingredients and targets of Phellodendri Chinensis Cortex were obtained through the BATMAN-TCM database, UC-related targets were searched by GeneCards database. The targets of Phellodendri Chinensis Cortex were corresponding to UC-related targets, the common targets and key active ingredients were screened. Cytoscape 3.8.2 software was used to construct the active ingredients-targets network, and a protein-protein interaction network was obtained by STRING database. GO function enrichment and KEGG signal pathway enrichment were analyzed by DAVID online tool. Results:A total of 26 active ingredients related to UC were obtained from Phellodendri Chinensis Cortex, and the key targets were DRD2, ESR1, NR3C1, ADRA2A and AR, which mainly involved in the Inflammatory mediator regulation of TRP channels, Sphingolipid Signaling pathways, cAMP and TNF signaling pathway by KEGG enrichment analysis. Conclusion:Phellodendri Chinensis Cortex can treat UC through a multi-ingredients, multi-targets and multi-pathways approach, which provides a new direction for future research.

倪明恺、华子春

医药卫生理论医学研究方法中医学

中药药理学网络药理学黄柏溃疡性结肠炎

pharmacology of Chinese materia medicanetwork pharmacologyPhellodendri Chinensis CortexUC

倪明恺,华子春.基于网络药理学的黄柏治疗溃疡性结肠炎机制探讨[EB/OL].(2021-08-12)[2025-08-04].http://www.paper.edu.cn/releasepaper/content/202108-28.点此复制

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