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中国药学(英文版) ›› 2023, Vol. 32 ›› Issue (5): 351-359.DOI: 10.5246/jcps.2023.05.030

• 【研究论文】 • 上一篇    下一篇

基于网络药理学方法探讨犀角地黄汤治疗系统性红斑狼疮的作用机制

王孟亚1, 张宽友2, 陈馨1, 付浩1,*(), 彭守春3,*()   

  1. 1. 武警特色医学中心, 天津 300162
    2. 天津市 河东区 东新街社区卫生服务中心, 天津 300162
    3. 天津市海河医院, 天津 300350
  • 收稿日期:2022-11-23 修回日期:2022-12-04 接受日期:2023-01-15 出版日期:2023-06-02 发布日期:2023-06-02
  • 通讯作者: 付浩, 彭守春
  • 作者简介:
    + Tel.: +86-22-61122977, E-mail:
    + Tel.: +86-22-60577216, E-mail:
  • 基金资助:
    The Scientific Research Projects of PLA (Grant No. 21JSZ23); Research Project of PAP (Grant No. CWJ18L004).

Study on the mechanism of Rhinoceros Horn and Rehmannia Decoction in the treatment of systemic lupus erythematosus based on the method of network pharmacology

Mengya Wang1, Kuanyou Zhang2, Xin Chen1, Hao Fu1,*(), Shouchun Peng3,*()   

  1. 1 Characteristic Medical Center of PAP, Tianjin 300162, China
    2 Dongxin Street Community Health Service Center, Hedong District, Tianjin 300162, China
    3 Haihe Hospital, Tianjin 300350, China
  • Received:2022-11-23 Revised:2022-12-04 Accepted:2023-01-15 Online:2023-06-02 Published:2023-06-02
  • Contact: Hao Fu, Shouchun Peng

摘要:

本研究通过网络药理学方法, 探讨犀角地黄汤治疗系统性红斑狼疮(SLE)的作用机制。首先通过TCMSP、TCMID和BATMAN-TCM数据库检索犀角地黄汤各中药成分的活性成分及其靶点, 汇总得到药物靶点; 其次在CTD、OMIM和TCMIP数据库检索得到SLE的疾病靶点, 并对药物靶点和疾病靶点的交集进行分析。利用Cytoscape 3.7.1软件构建药物-成分-靶点-疾病网络。在String平台构建治疗靶点的蛋白质互作网络(PPI), 筛选其关键模块和Hub基因, 在DAVID数据库进行GO和KEGG富集分析。最终筛选出22个犀角地黄汤的活性成分, 209个药物靶点, 284个疾病靶点, 59个治疗靶点。药物-成分-靶点-疾病网络和PPI网络分析得到槲皮素、山奈酚、黄芩素等核心活性成分, PTGS2、CASP3、MMP9、AKT1、JUN、CXCL8、FOS、TP53等核心靶点。主要涉及TNF、PI3K-Akt、Toll样受体、T细胞受体、细胞凋亡等信号通路。研究表明犀角地黄汤可能通过调控炎症、免疫及细胞凋亡等信号通路, 发挥抗炎、抑制异常免疫应答和细胞凋亡的作用, 具有多中心、多靶点、多途径的特点。

关键词: 系统性红斑狼疮, 网络药理学, 犀角地黄汤, 靶点

Abstract:

In the present study, we aimed to explore the mechanism of Rhinoceros Horn and Rehmannia Decoction in treating systemic lupus erythematosus (SLE). First, the active ingredients and their targets of the Chinese medicine components of Rhinoceros Horn and Rehmannia Decoction were searched through TCMSP, TCMID, and BATMAN-TCM databases, and then the drug targets were summarized. Then the disease targets of SLE were retrieved from CTD, OMIM, and TCMIP databases, and the intersection of drug targets and disease targets was analyzed. Cytoscape 3.7.1 software was used to construct a drug-component target-disease network. The protein-protein interaction (PPI) network of therapeutic targets was constructed on the String platform, and its key modules and hub genes were screened. GO and KEGG enrichment analyses were performed in the DAVID database. A total of 22 active ingredients, 209 drug targets, 284 disease targets, and 59 therapeutic targets were screened out. Drug-component-target-disease and PPI network analysis yielded core active ingredients, such as quercetin, kaempferol, and baicalein, and core targets, such as PTGS2, CASP3, MMP9, AKT1, JUN, CXCL8, FOS, and TP53. It mainly involves TNF, PI3K Akt, Toll-like receptor, T cell receptor, and apoptosis signal pathways. It can be seen that Rhinoceros Horn and Rehmannia Decoction may play the role of anti-inflammation, inhibition of abnormal immune response, and apoptosis by regulating inflammation, immunity, and apoptosis signaling pathways. It has the characteristics of multi-center, multi-target, and multi-pathway.

Key words: Systemic lupus erythematosus, Network pharmacology, Rhinoceros Horn and Rehmannia Decoction, Target

Supporting: