首页|基于网络药理学及分子对接探讨四逆散对溃疡性结肠炎与抑郁症"异病同治"的作用机制

基于网络药理学及分子对接探讨四逆散对溃疡性结肠炎与抑郁症"异病同治"的作用机制

扫码查看
目的 基于网络药理学及分子对接探讨四逆散对溃疡性结肠炎与抑郁症"异病同治"的作用机制.方法 利用TCMSP数据库获取四逆散的潜在活性成分及其相关作用靶点;利用GeneCards、CTD、TTD数据库筛选溃疡性结肠炎和抑郁症的疾病相关靶点;对上述预测得到的活性成分作用靶点与疾病相关靶点取交集,获得四逆散治疗溃疡性结肠炎和抑郁症的潜在作用靶点(共有靶点),采用Cytoscape 3.7.2 软件构建"中药-活性成分-疾病-共有靶点"网络,分析核心成分;将共有靶点导入STRING数据库,构建共有靶蛋白相互作用(PPI)网络,分析关键靶点;通过DAVID数据库对共有靶点进行GO功能及KEGG通路富集分析;对核心成分与关键靶点进行分子对接验证.结果 共获得四逆散的活性成分 136 个,四逆散治疗溃疡性结肠炎和抑郁症的潜在作用靶点(共有靶点)220 个,涉及 657 个生物过程、70 个细胞组分、147 个分子功能以及 133 条信号通路.筛选得到槲皮素、山柰酚、木犀草素、柚皮素、7-甲氧基-2-甲基异黄酮等核心活性化合物,JUN、MAPK3、STAT3、AKT1、MAPK1 等关键靶蛋白,以及TNF、IL-17、Th17 细胞分化、HIF-1、Toll样受体等信号通路.5 个关键靶点均与槲皮素、山柰酚、木犀草素、柚皮素有较强的结合活性.结论 四逆散可能是通过槲皮素、山柰酚、木犀草素、柚皮素等活性成分,作用于JUN、MAPK3、STAT3、AKT1、MAPK1 等关键靶点,通过TNF、IL-17、HIF-1、Toll样受体、Th17 细胞分化等信号通路,发挥对溃疡性结肠炎与抑郁症"异病同治"的作用.
Exploring the Mechanism of Sini San Formula on Ulcerative Colitis and Depression Through"Homotherapy for Heteropathy"Based on Network Pharmacology and Molecular Docking
Objective To investigate the mechanism of Sini San Formula in the treatment of ulcerative colitis and depression through"homotherapy for heteropathy"based on network pharmacology and molecular docking.Methods The TCMSP database was used to obtain the potential active components and their related targets;GeneCards,CTD,and TTD databases were used to screen the disease-related targets of ulcerative colitis and depression;the intersection of the predicted targets of the active components and the disease-related targets was used to obtain the potential targets(shared targets)for the treatment of ulcerative colitis and depression by Sini San Formula,and Cytoscape 3.7.2 software to construct a"Chinese medicinals-active components-diseases-common targets"network to analyze the core components;importing the common targets into the STRING database,constructing a common protein-protein interaction(PPI)network.The GO function and KEGG pathway enrichment of the shared targets were analyzed by DAVID database,and molecular docking between the core components and the key targets was verified.Results A total of 136 active components of Sini San Formula were obtained,and 220 potential targets of action(shared targets)for the treatment of ulcerative colitis and depression by Sini San Formula,involving 657 biological processes,70 cellular components,147 molecular functions and 133 signaling pathways.The screening yielded core active compounds such as quercetin,kaempferol,lignans,naringenin,7-methoxy-2-methylisoflavone,key target proteins such as JUN,MAPK3,STAT3,AKT1,and MAPK1,as well as signaling pathways such as TNF,IL-17,Th17 cellular differentiation,HIF-1,and Toll-like receptor.Five potential key targets have strong binding activity to quercetin,kaempferol,lignans and naringenin.Conclusion Sini San Formula may act on key targets such as JUN,MAPK3,STAT3,AKT1,MAPK1,etc.through active components such as quercetin,kaempferol,lignocerotonin,naringenin,etc.,and play the role of"homotherapy for heteropathy"for ulcerative colitis and depression through the signaling pathways such as TNF,IL-17,HIF-1,Toll-like receptor and Th17 cell differentiation.

Sini San Formulaulcerative colitisdepressionhomotherapy for heteropathynetwork pharmacologymolecular dockingmechanisms

单佳铃、胡伟琼、谢勤、白薇、胡田彧、吕燕妮、江明金

展开 >

南昌大学第一附属医院,江西 南昌 330006

复旦大学附属肿瘤医院闵行分院,上海 200240

江西省肿瘤医院,江西 南昌 330029

四逆散 溃疡性结肠炎 抑郁症 异病同治 网络药理学 分子对接 作用机制

国家自然科学基金江西省自然科学基金江西省自然科学基金江西省教育厅科技项目江西省卫生计生委科技项目江西省中医药局科技项目

8176072420171BAB21506720181BAB205026GJJ160129201810442017A287

2024

中药新药与临床药理
广州中医药大学

中药新药与临床药理

CSTPCD北大核心
影响因子:0.908
ISSN:1003-9783
年,卷(期):2024.35(1)
  • 10