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网络药理学和分子对接探索四妙汤治疗痛风性关节炎的潜力及作用机制。

Network pharmacology and molecular docking to explore the treatment potential and molecular mechanism of Si-Miao decoction against gouty arthritis.

机构信息

Orthopedics (Orthopedic Group), The Second Affiliated Hospital of Hunan University of Chinese Medicine, Changsha, China.

Hunan University of Chinese Medicine, Changsha, China.

出版信息

Medicine (Baltimore). 2024 May 31;103(22):e38221. doi: 10.1097/MD.0000000000038221.

Abstract

Gouty arthritis (GA) is a common metabolic rheumatological disease. Si-Miao decoction has therapeutic effects on GA. In our study, we investigated the mechanism of Si-Miao decoction against GA using network pharmacology and molecular docking analytical methods. The Traditional Chinese Medicine Systems Pharmacology Database was used as the basis for screening the main targets and agents of the Si-Miao decoction, and the Genecards, OMIM, and Drugbank databases were used to screen GA-related targets. They were analyzed using Venn with the drug targets to obtain the intersection targets. We used Cytoscape 3.9.1 to draw the "Drugs-Compounds-Targets" network and the String database for creative protein-protein interaction networks of target genes and filtered core targets. Gene Ontology and Kyoto Encyclopedia of Genes and Genomes were used to analyze the core targets. Molecular docking was performed using AutoDockTools to predict the binding capacity between nuclear targets and active components in the Si-Miao decoction. A total of 50 chemically active components containing 53 common targets of Si-Miao decoction anti-GA and 53 potential drug target proteins were identified. Core targets, namely, TNF, STAT3, SRC, PPARG, TLR4, PTGS2, MMP9, RELA, TGFB1, and SIRT1, were obtained through PPI network analysis. GO and KEGG analyses showed that the mechanism of anti-GA in Si-Miao decoction may proceed by regulating biological processes such as inflammatory factor levels, cell proliferation, apoptosis, and lipid and glucose metabolism, and modulating the NOD-like receptor signaling pathway, IL-17 signaling pathway, TNF signaling pathway, NF-kappa B signaling pathway, and Toll-like receptor signaling pathway. We further screened the core targets, including PTGS2, MMP9, and PPAGR, as receptor proteins based on their degree value and molecular docking with the main active compounds in Si-Miao decoction, and found that baicalein had high affinity. In conclusion, Si-Miao decoction, through anti-inflammatory, apoptosis-regulating, and anti-oxidative stress action mechanisms in the treatment of GA.

摘要

痛风性关节炎(GA)是一种常见的代谢性风湿病。四妙汤对 GA 有治疗作用。在我们的研究中,我们使用网络药理学和分子对接分析方法研究了四妙汤治疗 GA 的机制。我们使用中药系统药理学数据库作为筛选四妙汤主要靶点和药物的基础,并使用 Genecards、OMIM 和 Drugbank 数据库筛选 GA 相关靶点。我们使用 Venn 分析药物靶点以获得交集靶点。我们使用 Cytoscape 3.9.1 绘制“药物-化合物-靶点”网络和 String 数据库的创新蛋白质-蛋白质相互作用网络的靶基因,并筛选核心靶基因。使用基因本体论和京都基因与基因组百科全书分析核心靶基因。使用 AutoDockTools 进行分子对接,预测核靶点与四妙汤中活性成分的结合能力。鉴定了 50 种含有 53 种四妙汤抗 GA 共同靶点和 53 种潜在药物靶点蛋白的化学活性成分。通过 PPI 网络分析获得核心靶点,即 TNF、STAT3、SRC、PPARG、TLR4、PTGS2、MMP9、RELA、TGFB1 和 SIRT1。GO 和 KEGG 分析表明,四妙汤抗 GA 的机制可能通过调节炎症因子水平、细胞增殖、凋亡、脂质和葡萄糖代谢等生物过程,调节 NOD 样受体信号通路、IL-17 信号通路、TNF 信号通路、NF-kappa B 信号通路和 Toll 样受体信号通路来进行。我们进一步筛选了核心靶点,包括 PTGS2、MMP9 和 PPARG,作为受体蛋白,基于它们的度值和与四妙汤主要活性化合物的分子对接,发现黄芩素具有高亲和力。总之,四妙汤通过抗炎、调节凋亡和抗氧化应激作用机制治疗 GA。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fef9/11142817/3e933bc5e889/medi-103-e38221-g001.jpg

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