麻杏石肝汤治疗流行性感冒的网络药理学研究

Q3 Medicine
Long Xi , Liu Le-Ping , Xu Xin-Yi , L.I. Ling , Zhang Guo-Min
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引用次数: 2

摘要

目的采用药理学方法筛选麻星湿肝汤治疗流感的靶点和信号通路,探讨其抗流感作用机制。方法在规定的条件下检索中药系统药理学数据库和分析平台(TCMSP)及相关文献,鉴定主要化合物及其靶点。使用STRING数据库预测目标蛋白之间的相互作用。利用WebGestalt和reactome数据库对流感蛋白-蛋白相互作用(PPI)网络中涉及的核心靶点进行基因本体(GO)功能富集分析和京都基因与基因组百科全书(KEGG)途径分析。iGEMDOCK用于受体与配体的分子对接,生成对接评分,并使用Autodock和PyMOL将结果可视化。结果共筛选出126个主要化合物及其靶点。利用STRING数据库预测了355个流感靶蛋白和1 221个流感蛋白相互作用。流感相关信号通路在MXSGD的药效学靶点如免疫系统细胞因子信号和白细胞介素信号中富集。主要的生物学过程是对刺激的反应。分子对接结果显示,MXSGD诱导的RELA-Licochalcone A对接优于其他靶蛋白和活性化合物,提示该对接位点也是MXSGD在流感治疗中的主要效应位点。结论MXSGD可能通过干扰病毒吸附、抑制病毒增殖、影响免疫功能、保护宿主细胞等途径发挥抗流感作用,从而预防炎症诱导的组织损伤。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A Network Pharmacology Study on the Effects of Ma Xing Shi Gan Decoction on Influenza

Objective

Pharmacological methods were used to screen targets and signaling pathways of Ma Xing Shi Gan Decoction (MXSGD) during influenza treatments, and mechanisms underlying anti-influenza effects were elucidated.

Methods

The Traditional Chinese Medicine Systems Pharmacology Database and Analysis Platform (TCMSP) and relevant literature were searched under predefined conditions to identify the main compounds and their targets. Interactions between the target proteins were predicted using the STRING database. Gene Ontology (GO) functional enrichment analyses and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analyses were performed on the core targets involved in the influenza protein-protein interaction (PPI) network, using WebGestalt and the reactome database. iGEMDOCK was used for molecular docking of receptors and ligands to produce docking scores, and the results were visualized using Autodock and PyMOL.

Results

In total, 126 major compounds and their respective targets were screened. 355 influenza target proteins and 1 221 influenza protein interactions were predicted using the STRING database. Influenza-related signaling pathways were strongly enriched in pharmacodynamic targets of MXSGD such as cytokine signaling in immune system and signaling by inter-leukin. The main biological process was response to the stimulates. Molecular docking results showed that RELA-Licochalcone A docking elicited by MXSGD, was superior to that of other target proteins and active compounds, suggesting that the docking site is also the main effector site of MXSGD during influenza treatments. Conclusions The results showed that MXSGD exerts anti-influenza effects by interfering with virus adsorption, inhibiting virus proliferation, influencing immune functions and protecting host cells, which may prevent inflammation-induced tissue damage.

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来源期刊
Digital Chinese Medicine
Digital Chinese Medicine Medicine-Complementary and Alternative Medicine
CiteScore
1.80
自引率
0.00%
发文量
126
审稿时长
63 days
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