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基于网络药理学探讨黄芪治疗病毒性胰腺炎的疗效及机制

曹星新 段素琴 侯婧涵 马骏驰 李艾亦 和占龙

中国比较医学杂志2025,Vol.35Issue(5):1-11,11.
中国比较医学杂志2025,Vol.35Issue(5):1-11,11.DOI:10.3969/j.issn.1671-7856.2025.05.001

基于网络药理学探讨黄芪治疗病毒性胰腺炎的疗效及机制

Network pharmacology analysis of efficacy and mechanism of Astragalus in the treatment of viral pancreatitis

曹星新 1段素琴 1侯婧涵 1马骏驰 1李艾亦 2和占龙1

作者信息

  • 1. 中国医学科学院/北京协和医学院医学生物学研究所,昆明 650018
  • 2. 云南大学生命科学学院,昆明 650500
  • 折叠

摘要

Abstract

Objective To explore the efficacy and underlying mechanism of Astragalus in the treatment of viral pancreatitis using network pharmacology,with confirmation of its efficacy and mechanism in cell experiments.Methods Astragalus and viral pancreatitis targets obtained from the Traditional Chinese Medicine Systems Pharmacology(TCMSP)and GeneCards databases were combined to obtain intersection targets.GO functional enrichment and KEGG signaling pathway enrichment analyses of therapeutic targets were conducted using the Database for Annotation,Visualization,and Integrated Discovery(DAVID)database.The interactions between therapeutic targets were analyzed using the STRING database and Cytoscape 3.10.2,and the core therapeutic targets were screened.Molecular docking between the most effective therapeutic components and the core targets was performed using PyMOL 3.0 and AutoDock Tools 1.5.7.CVB3 was used to construct a viral pancreatitis cell model for verification of the core targets.Results Seventy-eight therapeutic targets were identified.Enrichment analyses revealed the possible involvement of pathways related to cancer,lipids and atherosclerosis,and PI3K-AKT signaling.AKT1,TP53,HIF1A,CASP3,IL-6,and MMP9 were identified as possible core targets.The result of cell experiments showed that the expression level of AMY was significantly increased in the model group(P<0.05).The Astragalus injection group exhibited significantly decreased expression levels of AMY,AKT1,TP53,HIF1A,CASP3,IL-6,and MMP9 compared with the model group(P<0.05).Conclusions Astragalus injection effectively treated viral pancreatitis,and its therapeutic mechanism may involve reduced expression levels of AKT1,TP53,HIF1A,CASP3,IL-6,and MMP9.

关键词

黄芪/柯萨奇病毒/病毒性胰腺炎/网络药理学/细胞实验

Key words

Astragalus/Coxsackie virus/viral pancreatitis/network pharmacology/cell experiment

引用本文复制引用

曹星新,段素琴,侯婧涵,马骏驰,李艾亦,和占龙..基于网络药理学探讨黄芪治疗病毒性胰腺炎的疗效及机制[J].中国比较医学杂志,2025,35(5):1-11,11.

基金项目

中国医学科学院医学与健康科技创新工程(2021-I2M-1-024) (2021-I2M-1-024)

云南省基础研究专项面上项目(202401CF070048). (202401CF070048)

中国比较医学杂志

OA北大核心

1671-7856

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