基于网络药理学探讨紫草素对肝损伤的作用

Journal: Basic Medical Theory Research DOI: 10.12238/bmtr.v6i4.8490

姬雨辰, 梁远锋, 陈雪, 耿昊东, 马磊, 梁丹丹

新疆第二医学院

Abstract

目的:基于网络药理学方法探究紫草素改善肝损伤的分子作用机制。方法:运用Traditional Chinese Medicine Systems Pharmacology(TCMSP)、Pharm-Mapper检索 紫草素作用的相关靶点,并将检索得到的靶点在Uniprot蛋白质数据库进行标准化处理;通过OMIM、GeneCards数据库获取肝损伤的有效靶点;通过Venny平台,得到的交集靶点作为紫草素治疗肝损伤的靶点,运用Cytoscape3.7.0软件和String数据库构建紫草素-肝损伤交集靶点网络以及蛋白-蛋白相互作用(protein-protein interaction,PPI)网络图;采用DAVID数据库对关键靶点进行基因本体GO富集分析和京都基因与基因组百科全书(KEGG)富集分析,阐述紫草素改善肝损伤的作用通路及分子机制。结果:通过TCMSP和Pharm-Mapper数据库,获得289个紫草素靶点,从OMIM及GeneCards数据库中筛选出9707个肝损伤靶点,通过Venny平台找到252个紫草素与肝损伤的共表达靶点,在PPI网络图中得到关键靶点为AKT1,EGFR,ESR1,CASP3等10个核心靶点,通过GO富集和KEGG通路分析,主要涉及内分泌代谢通路、癌症通路、PI3K-Akt信号通路、Ras信号通及MAPK信号通路等。结论:紫草素可通过靶向AKT1,EGFR,ESR1,CASP3等多靶点和多途径的方式发挥改善肝损伤的作用。

Keywords

紫草素;肝损伤;网络药理学

Funding

新疆维吾尔自治区级大学生创新创业训练计划项目(No.S202213560017)。

References

[1] Devarbhavi, Harshad et al.“Global burden of liver disease:2023 update.”Journal of hepatology vol.79,2(2023):516-537.
[2] You,Jingping etal.“Lentinan induces apoptosis of mouse hepatocellular carcinoma cells through the EGR1/PTEN/A KT signaling axis.” Oncology reports vol.50,1(2023):142.
[3] Ma,Xiao-Yaoetal. “Ursolic acid reduces hepatocellular apoptosis and alleviates alcohol-induced liver injury via irreversible inhibition of CASP3 in vivo.” Acta pharmacologica Sinica vol.42,7(2021):1101-1110.
[4] Pallerla,Pavankumar etal.“Evaluation of amino acids and other related metabolites levels in end-stage renal disease (ESRD) patients on hemodialysis by LC/MS/MS and GC/MS.” Analytical and bioanalytical chemistry vol.415,26(2023):6491-6509.
[5] Meng,Yu-Xietal.“Interleukin-22 alleviates alcoholassociated hepatic fibrosis, inhibits autophagy, and suppres ses the PI3K/AKT/mTOR pathway in mice.” Alcohol, clinical & experimental research vol.47,3(2023):448-458.

Copyright © 2024 姬雨辰, 梁远锋, 陈雪, 耿昊东, 马磊, 梁丹丹

Creative Commons License
This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License