首页|基于网络药理学分析"淫羊藿-当归"治疗骨质疏松症的作用机制

基于网络药理学分析"淫羊藿-当归"治疗骨质疏松症的作用机制

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目的 基于网络药理学方法探究"淫羊藿-当归"配伍在治疗骨质疏松症(OP)过程中有效成分和作用机制.方法 运用中药系统药理学数据库与分析平台(TCMSP)获取"淫羊藿-当归"配伍有效成分及相对应的预测靶点;通过GeneCards、OMIM、PharmGkb、TTD、DrugBank 5 个数据库获取OP靶基因,将以上 5 个数据库所获取的基因合并取交集,然后将"淫羊藿-当归"和OP 的潜在作用靶点取交集,得到"药物-疾病"共有靶点.并用Venny 2.1.0作图工具找出映射,绘制 VENN图;通过 String 11.5 数据库建立蛋白-蛋白相互作用(PPI);通过 Cytoscape 3.9.1软件构建相关数据分析网络,筛选出核心靶基因;最后利用DAVID2021 数据库对关键靶基因进行富集分析,并用微生信在线绘图软件对已分析的靶基因数据进行GO和京都基因及基因组百科全书(KEGG)通路的可视化绘图.结果 获得"淫羊藿-当归"药对涉及 22 个主要化学成分和 129 个蛋白靶点,OP相关基因 1159 个,映射后获得药物与疾病共有靶点 74 个;PPI分析显示白细胞介素-1B(IL-1B)、V-Jun肉瘤病毒癌基因同源物(JUN)重组蛋白、丝/苏氨酸蛋白激酶(AKT1)等可能是"淫羊藿-当归"药对治疗OP的核心靶点;GO富集分析提示生物学过程主要包括RNA聚合酶Ⅱ启动子转录的正向调控、基因表达的正向调控等;KEGG通路富集分析提示"淫羊藿-当归"治疗OP作用主要集中在高级糖基化终末产物-受体(AGE-RAGE)、磷脂酰肌醇 3 激酶/蛋白激酶B(PI3K-Akt)、有丝裂原活化蛋白激酶(MAPK)、白细胞介素-17(IL-17)等信号通路.结论 "淫羊藿-当归"配伍可以通过多途径、多靶点治疗OP.
Mechanism of Action of"Epimedium-Angelica"in the Treatment of Asteoporosis Based on the Analysis of Network Pharmacology
Objective To explore the active components and mechanism of"Epimedium-Angeli-ca"in the treatment of osteoporosis(OP).Methods The Traditional Chinese Medicine Systems Pharmacology Database and Analysis Platform(TCMSP)was utilized to obtain the active ingre-dients and the corresponding predicted targets of"Epimedium-Angelica".The target genes of OP were obtained from five databases:GeneCards,OMIM,PharmGkb,TTD,and DrugBank.The genes obtained from the above five databases were combined and intersected.Then the poten-tial targets of"Epimedium-Angelica"and OP were intersected to obtain the"drug-disease"common targets.The Venny 2.1.0 mapping tool was used to find out the mapping and draw the venn diagram.Protein-protein interac-tion(PPI)was established by String 11.5 database.The relevant data analysis network was constructed by Cytoscape 3.9.1 software to screen the core target genes.Finally,the key target genes were enriched and analyzed using the DAVID2021 da-tabase,and the analyzed target gene data were visualized and mapped for GO and Kyoto Ency-clopedia of Genes and Genomes(KEGG)pathways using the Microbiotics online mapping soft-ware.ResultThe Epimedium-Angelica drug pairs involved 24 major chemical components and 129 protein targets,1159 genes associated to osteoporosis.After mapping,74 common targets of drugs and diseases were obtained.PPI analysis revealed that interleukin-1B(interleukin-1B,IL-1B),JUN,filament/threonine protein kinase AKT 1(AKT 1)may be the core targets of"Epimedium-Angelica"drugs for the treatment of OP.GO enrichment analysis suggests that bio-logical processes mainly include the positive regulation of RNA polymerase Ⅱ promoter transcrip-tion and the positive regulation of gene expression.KEGG pathway enrichment analysis suggested that the effects of"Epimedium-Angelica"in the treatment of osteoporosis mainly focused on advanced glycation end product-receptor(AGE-RAGE),phosphatidylinositol 3 kinase/protein kinase B(PI3K-Akt),mitogen-activated protein kinase(mitogen-activated protein kinase,MAPK),interleukins-17(Interleukin-17,L-17)and other signaling pathways.Conclusion The compatibility of Epimedium-Angelica can treat osteoporosis through multiple ways and targets.

network pharmacologyosteoporosisEpimediumAngelicamechanism of action

李志平、李建军

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天水市中医医院脑病二科(甘肃 天水 741000)

网络药理学 骨质疏松 淫羊藿 当归 作用机制

国家自然科学基金

82160911

2024

湖北民族大学学报(医学版)

湖北民族大学学报(医学版)

ISSN:
年,卷(期):2024.41(1)
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