基于网络药理学-分子对接技术探讨清瘟败毒饮对川崎病、过敏性紫癜及系统性红斑狼疮的异病同治作用机制
DOI:
CSTR:
作者:
作者单位:

作者简介:

通讯作者:

中图分类号:

R285

基金项目:


Explore the Mechanism of Treating Different Diseases with Same Method of Qingwen Baidu Decoction in Treating Kawasaki Disease, Henoch-Schonlein Purpura and Systemic Lupus Erythematosus Base on Network Pharmacology Combined with Molecular Docking Technology
Author:
Affiliation:

Fund Project:

  • 摘要
  • |
  • 图/表
  • |
  • 访问统计
  • |
  • 参考文献
  • |
  • 相似文献
  • |
  • 引证文献
  • |
  • 资源附件
  • |
  • 文章评论
    摘要:

    目的:基于中医“异病同治”理论,通过网络药理学及分子对接方法研究清瘟败毒饮治疗川崎 病(KD)、过敏性紫癜(HSP)和系统性红斑狼疮(SLE)的作用成分、作用靶点、作用通路,为基础研究和 临床运用提供理论依据。方法:将中药系统药理学数据库与分析平台 (TCMSP)、中医药百科全书数据 库 (ETCM) 筛选出的清瘟败毒饮靶点与 Gencards、OMIM 数据库获取的 KD、HSP 和 SLE 疾病靶点取得交 集;利用 String 数据库、Cytoscape 绘制蛋白互作图(PPI),CytoHubba 分析获得核心作用靶点;利用 DAVID 数据库及 R 语言进行 GO 和 KEGG 富集分析;通过 Cytoscape 构建药物-成分-靶点-通路网络图,获得核心成 分;利用 AutoDock、PyMOL 进行分子对接。结果:清瘟败毒饮中有 6 个有效成分通过调控 38 个靶点以及 123 条通路可同时对 KD、HSP 和 SLE 产生作用,主要是槲皮素、芹黄素、山柰酚、木犀草素、β-谷甾醇、汉 黄芩素等通过白细胞介素-6、血管内皮生长因子、过氧化物酶增殖物激活受体 γ 等核心靶点作用脂质与动脉 粥样硬化通路、癌症通路等通路从而起治疗作用;分子对接结果提示大部分靶点和成分的结合活性较好。 结论:清瘟败毒饮“异病同治”KD、HSP 和 SLE 具有多成分、多有效靶点、多通路协调作用特点,也反向证 实了中医“异病同治”理论科学性和有效性,为进一步开展治疗 KD、HSP 和 SLE 基础研究和临床试验提供新 的思路。

    Abstract:

    Abstract: Objective: To study the active components, targets and pathways of Qingwen Baidu Decoction in the treatment of Kawasaki disease (KD),Henoch-schonlein purpura (HSP) and systemic lupus erythematosus (SLE),through the network pharmacology and molecular docking method,based on the theory of "treating different diseases with same method" in traditional Chinese medicine (TCM),so as to provide theoretical basis for basic research and clinical application for these diseases. Methods:The targets of Qingwen Baidu Decoction selected from Traditional Chinese Medicine Systems Pharmacology Database and Analysis Platform (TCMSP) and the Encyclopedia of Traditional Chinese Medicine (ETCM) databases were intersected with KD,HSP and SLE disease targets obtained from Gencards and OMIM databases. The protein-protein interaction (PPI) diagram was drawn by using String database and Cytoscape,and the core targets were obtained by CytoHubba analysis. DAVID database and R language were used to conduct GO and KEGG enrichment analysis. Core components were obtained by constructing drug-component- target- pathway network diagram through Cytascape. AutoDock and PyMOL were used for molecular docking. Results:There were six active components in Qingwen Baidu Decoction that can simultaneously affect KD, HSP and SLE by regulating 38 targets and 123 pathways. Mainly Quercetin, Apigenin, Kaempferol,Luteolin,β-sitosterol,Baicalin,which played the therapeutic role by acting on lipid and atherosclerosis pathways, cancer pathways and other pathways through the core targets such as interleukin- 6, vascular endothelial growth factor, and peroxidase proliferators γ, etc. The molecular docking results suggested that most of the targets and components have good binding activity. Conclusion: The "treating different diseases with same method" for KD,HSP,and SLE of Qingwen Baidu Decoction have the characteristics of multiple components,multiple effective targets,and coordinated effects of multiple pathways. It also confirms the scientific and effective nature of the TCM theory of "treating different diseases with same method" has provided new ideas for further basic research and clinical trials on the treatment of KD,HSP,and SLE.

    参考文献
    相似文献
    引证文献
引用本文

吴邹平,李鲜慧,黄秋琪,吉训超.基于网络药理学-分子对接技术探讨清瘟败毒饮对川崎病、过敏性紫癜及系统性红斑狼疮的异病同治作用机制[J].新中医,2023,55(15):8-16

复制
分享
文章指标
  • 点击次数:
  • 下载次数:
  • HTML阅读次数:
  • 引用次数:
历史
  • 收稿日期:
  • 最后修改日期:
  • 录用日期:
  • 在线发布日期: 2023-08-13
  • 出版日期:
文章二维码