首页|赤茵合剂介导丝裂原活化蛋白激酶相关通路改善慢性乙型肝炎肝纤维化的网络药理学研究

赤茵合剂介导丝裂原活化蛋白激酶相关通路改善慢性乙型肝炎肝纤维化的网络药理学研究

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目的:以网络药理学和分子对接技术为依托,探究安徽中医药大学第一附属医院院内制剂赤茵合剂治疗慢性乙型肝炎(Chronic Hepatitis B,CHB)肝纤维化的相关作用机制.方法:运用中药系统药理学分析平台(TC-MSP)检索并下载组成赤茵合剂各味药的潜在有效活性成分及在人体内对应靶点,从Genecards、OMIM、DrugBank、PharmGkb、TTD数据库中检索并下载CHB肝纤维化的靶点,使用Venn在线作图软件获取药物与疾病的共同靶点并绘制Venn图,应用String数据库建立共同靶点之间的蛋白互作(PPI)网络,使用Cytoscape软件中的CytoNCA插件获取PPI网络中的关键靶点,利用R包对交集靶点进行GO功能富集分析,以同样方法获取KEGG通路富集分析结果.使用Cytoscape软件构建"药物-疾病-靶点-通路"网络图,通过分析"药物-疾病-靶点-通路"网络获取关键活性成分,使用AutoDock Vina软件将筛选后的赤茵合剂关键活性成分与疾病-药物关键靶点逐一进行模拟分子对接.结果:筛选出赤茵合剂化合物共计202个,有效作用靶点298个.通过Venn图获得282个药物-疾病共同靶点,PPI网络发现JUN、MAPK3、TP53、AKT1、MAPK1、MAPK14等可能是赤茵合剂治疗CHB肝纤维化的关键靶点.GO分析共包含3120条富集结果,KEGG通路分析发现191条通路富集结果.分子对接结果显示赤茵合剂可能通过TP53、MAPK3、MAPK14途径干预CHB肝纤维化的活动从而达到治疗效果.结论:赤茵合剂通过"多成分-多靶点-多途径"发挥了治疗CHB肝纤维化的作用.赤茵合剂中槲皮素、大豆黄酮、柚皮素、黄芩素、大黄素、木犀草素、葛根素、丹参素、丹参酮ⅡA等10种活性成分值得后续研究重点关注.全文多方面整合分析,推测赤茵合剂通过介导丝裂原活化蛋白激酶经由PI3K/AKT通路发挥了改善CHB肝纤维化的作用.
Network Pharmacology Study of Chiyin Mixture Mediating Mitogen-activated Protein Kinase-related Pathway to Improve CHB Liver Fibrosis
Objective:Based on network pharmacology and molecular docking technology,to explore the relevant mechanism of action of Chiyin Mixture,an in-hospital preparation of the First Affiliated Hospital of Anhui University of Traditional Chinese Medicine,in the treatment of chronic hepatitis B liver fibrosis.Methods:The Traditional Chinese Medicine Systems Pharmacology Analysis Platform(TCMSP)was used to search and download the potentially effective active ingredients of each medicine in Chiyin Mixture and the corresponding targets in the human body,and search and download from Genecards,OMIM,DrugBank,PharmGkb,and TTD databases.For the targets of chronic hepatitis B liv-er fibrosis,use Venn online mapping software to obtain common targets of drugs and diseases and draw Venn diagrams,use String database to establish protein interaction(PPI)networks between common targets,and use Cytoscape The CytoNCA plug-in in the software obtains the key targets in the PPI network,uses the R package to perform GO func-tional enrichment analysis on the intersection targets,and obtains the KEGG pathway enrichment analysis results in the same way.Use Cytoscape software to construct a"drug-disease-target-pathway"network diagram,obtain key ac-tive ingredients by analyzing the"drug-disease-target-pathway"network,and use AutoDock Vina software to compare the screened key active ingredients of Chiyin Mixture with Disease-key drug targets are simulated molecular docking one by one.Results:A total of 202 compounds of the Chiyin mixture were screened out,with 298 effective targets.282 drug-disease common targets were obtained through the Venn diagram,and the PPI network found that JUN,MAPK3,TP53,AKT1,MAPK1,MAPK14,etc.may be the key targets of Chiyin Mixture in the treatment of chronic hepatitis B liver fibrosis.GO analysis contained a total of 3120 enrichment results,and KEGG pathway analysis found 191 pathway enrichment results.Molecular docking results show that Chiyin Mixture may intervene in the activities of chronic hepa-titis B liver fibrosis through the TP53,MAPK3,and MAPK14 pathways to achieve therapeutic effects.Conclusion:Chi-yin mixture plays a role in treating CHB liver fibrosis through"multi-component-multi-target-multi-pathway".The 10 active ingredients in the red yeast mixture,including quercetin,daidzein,naringenin,baicalein,emodin,luteolin,puerarin,tanshinol,and tanshinone ⅡA,deserve the focus of subsequent research.Through multi-faceted integrated analysis of the full text,it is speculated that Chiyin Mixture plays a role in improving CHB liver fibrosis by mediating mitogen-activated protein kinase through the PI3K/AKT pathwav.

Chiyin mixtureChronic hepatitis BLiver fibrosisNetwork pharmacologyMolecular docking

孙宇洁、施卫兵、许文彬、马翠翠、储茂锋、赵漫玲

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安徽中医药大学第一临床医学院 安徽合肥 230038

安徽中医药大学第一附属医院 安徽合肥 230038

赤茵合剂 慢性乙型肝炎 肝纤维化 网络药理学 分子对接

长三角名中医工作室建设项目安徽省施卫兵名中医工作室建设项目

皖财社[2021]324号安徽省卫健委中发展[2020]10号

2024

中医药临床杂志
中华中医药学会

中医药临床杂志

影响因子:0.636
ISSN:1672-7134
年,卷(期):2024.36(6)