[Exploration of pharmacodynamic substances and potential mechanisms of Huazhuo Sanjie Chubi Decoction in treatment of gouty arthritis based on UPLC-Q-Exactive Orbitrap-MS technology and network pharmacology].

Q3 Pharmacology, Toxicology and Pharmaceutics
Yan Xiao, Ting Zhang, Ying-Jie Zhang, Bin Huang, Peng Chen, Xiao-Hua Chen, Ming-Qing Huang, Xue-Ting Chen, You-Xin Su, Jie-Mei Guo
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引用次数: 0

Abstract

Based on ultra-high performance liquid chromatography-quadrupole-Exactive Orbitrap mass spectrometry(UPLC-Q-Exactive Orbitrap-MS) technology and network pharmacology, this study explored the pharmacodynamic substances and potential mechanisms of Huazhuo Sanjie Chubi Decoction in the treatment of gouty arthritis(GA). UPLC-Q-Exactive Orbitrap-MS technology was used to identify the components in Huazhuo Sanjie Chubi Decoction, and the qualitative analysis of its active ingredients was carried out, with a total of 184 active ingredients identified. A total of 897 active ingredient targets were screened through the PharmMapper database, and 491 GA-related disease targets were obtained from the OMIM, GeneCards, CTD databases. After Venn analysis, 60 intersecting targets were obtained. The component target-GA target network was constructed through the Cytoscape platform, and the STRING database was used to construct a protein-protein interaction network, with 16 core targets screened. The core targets were subjected to Gene Ontology(GO) and Kyoto Encyclopedia of Genes and Genomes(KEGG) pathway enrichment analyses, and the component-target-pathway network was constructed. It was found that the main active ingredients of the formula for the treatment of GA were phenols, flavonoids, alkaloids, and terpenoids, and the key targets were SRC, MMP3, MMP9, REN, ALB, IGF1R, PPARG, MAPK1, HPRT1, and CASP1. Through GO analysis, it was found that the treatment of GA mainly involved biological processes such as lipid response, bacterial response, and biostimulus response. KEGG analysis showed that the pathways related to the treatment of GA included lipids and atherosclerosis, neutrophil extracellular traps(NETs), IL-17, and so on. In summary, phenols, flavonoids, alkaloids, and terpenoids may be the core pharmacodynamic substances of Huazhuo Sanjie Chubi Decoction in the treatment of GA, and the pharmacodynamic mechanism may be related to SRC, MMP3, MMP9, and other targets, as well as lipids and atherosclerosis, NETs, IL-17, and other pathways.

[基于UPLC-Q-Exactive Orbitrap-MS技术和网络药理学的化浊散结除痹汤治疗痛风性关节炎的药理学物质及潜在机制探索]。
本研究基于超高效液相色谱-四极萃取轨道阱质谱(UPLC-Q-Exactive Orbitrap- ms)技术和网络药理学,探讨化浊散结除痹汤治疗痛风性关节炎(GA)的药效物质及可能机制。采用UPLC-Q-Exactive Orbitrap-MS技术对花浊散结除痹汤中的成分进行了定性分析,共鉴定出184种有效成分。通过PharmMapper数据库共筛选了897个活性成分靶点,并从OMIM、GeneCards、CTD数据库获得了491个ga相关疾病靶点。经维恩分析,得到60个相交目标。通过Cytoscape平台构建组分靶点- ga靶点网络,利用STRING数据库构建蛋白-蛋白相互作用网络,筛选出16个核心靶点。对核心靶点进行基因本体(GO)和京都基因与基因组百科全书(KEGG)途径富集分析,构建组分-靶点-途径网络。结果发现,该配方对赤霉素的主要有效成分为酚类、黄酮类、生物碱类和萜类,关键靶点为SRC、MMP3、MMP9、REN、ALB、IGF1R、PPARG、MAPK1、HPRT1和CASP1。通过氧化石墨烯分析发现,GA的治疗主要涉及脂质反应、细菌反应和生物刺激反应等生物过程。KEGG分析显示与GA治疗相关的通路包括脂质和动脉粥样硬化、中性粒细胞胞外陷阱(NETs)、IL-17等。综上所述,酚类、黄酮类、生物碱、萜类可能是化浊散结除痹汤治疗GA的核心药效学物质,其药效学机制可能与SRC、MMP3、MMP9等靶点以及脂质与动脉粥样硬化、NETs、IL-17等途径有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Zhongguo Zhongyao Zazhi
Zhongguo Zhongyao Zazhi Pharmacology, Toxicology and Pharmaceutics-Pharmacology, Toxicology and Pharmaceutics (all)
CiteScore
1.50
自引率
0.00%
发文量
581
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