首页|基于网络药理学探究丹溪痛风方在痛风性关节炎中的抗炎作用

基于网络药理学探究丹溪痛风方在痛风性关节炎中的抗炎作用

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目的 利用网络药理学、分子对接技术及动物实验探究丹溪痛风方(DanxiTongfeng Decoction,DXTFD)治疗痛风性关节炎(Gouty arthritis,GA)的抗炎作用及机制.方法 使用TCMSP数据库筛选DXTFD活性成分和靶点;通过TTD、Drug-Bank、OMIM以及GeneCards数据库筛选GA相关靶点;取交集后,利用Cytoscape 3.8.0 和STRING数据库构建PPI网络;将核心靶点通过R语言进行GO富集分析和KEGG通路富集分析.运用AutodockVina 1.5.7 进行分子对接,预测有效成分和疾病靶点的结合能力.针对网络药理学筛选的部分核心靶点(IL-6、IL-8),我们设计了GA大鼠模型动物实验,检测了GA大鼠模型滑膜组织的病理形态及血清炎症因子(IL-6、IL-8)水平,进一步验证丹溪痛风方治疗痛风性关节炎的抗炎作用及机制.结果 筛选获得DXTFD活性成分 132 个,靶点 776 个,疾病靶点 375 个,交集靶点 99 个;GO富集分析主要在炎症反应、类固醇代谢、脂肪酸代谢等生物学调控方面;KEGG富集分析得到信号通路 132 条,主要涉及NOD样受体信号通路;活性成分香叶木素、黄芩素与TNF、IL6、PTGS2、MAPK3 靶点结合能力良好;动物实验表明,DXTFD可以通过抑制GA大鼠体内炎症因子IL-6、IL-8 的表达发挥药效.结论 DXTFD可能通过多成分、多靶点抑制炎症反应防治痛风性关节炎.
Exploration of the anti-inflammatory mechanism of Danxi gout formula in gouty arthritis based on net-work pharmacology
Objective To explore the anti-inflammatory effect and mechanism of DanxiTongfeng Decoction(DXTFD)in the treatment of gouty arthritis(GA)with network pharmacology,molecular docking technology and animal experiments.Methods The TCMSP database was used to identify active components and targets of DXTFD;TTD,DrugBank,OMIM,and GeneCards databases were used to screen for GA-related targets.After obtaining the intersection of these targets,a protein-protein interaction(PPI)network was constructed using Cytoscape3.8.0 and STRING databases.Core targets were subjected to GO enrichment analysis and KEGG pathway en-richment analysis using R language.Molecular docking was performed with AutodockVina 1.5.7 to predict the binding ability of active components and disease targets.For some of the core targets of network pharmacology screening(IL-6,IL-8),we designed GA rat model animal experiment to detect the pathomorphology and serum inflammatory factors(IL-6,IL-8)of GA rat model to further verify the anti-inflammatory effect and mechanism of Danxi gout prescription in the treatment of gouty arthritis.Results A total of 132 DXT-FD active ingredients and 776 targets were identified for DXTFD,with 375 disease targets and 99 intersection targets.GO enrichment a-nalysis indicated significant involvement in inflammatory response,steroid metabolism,fatty acid metabolism and other biological regula-tion.KEGG enrichment analysis revealed 132 signaling pathways,involved in the NOD-Like receptor signaling pathway.The active in-gredients gerloin and baicalein demonstrated strong binding ability with TNF,IL-6,PTGS2 and MAPK3 targets.Animal experiments in-dicated that DXTFD could exert therapeutic effects by inhibiting the expression of inflammatory cytokines IL-6 and IL-8 in GA rats.Conclusion DXTFD may prevent and treat GA by inhibiting inflammation with multiple components and multiple targets.

Danxi gout prescriptiongouty arthritisnetwork pharmacologymolecular dockinganti-inflammatory effect

王书惠、高丹、王栋、韩洁茹、白吉祥

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牡丹江医科大学附属红旗医院

牡丹江医科大学,黑龙江 牡丹江 157011

黑龙江中医药大学,黑龙江 哈尔滨 150040

丹溪痛风方 痛风性关节炎 网络药理学 分子对接 抗炎作用

2025

牡丹江医学院学报
牡丹江医学院

牡丹江医学院学报

影响因子:0.615
ISSN:1001-7550
年,卷(期):2025.46(1)