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Anti-Inflammatory Activity of Sanjie Zhentong Capsule Assessed By Network Pharmacology Analysis of Adenomyosis Treatment

机译:三杰振通胶囊的抗炎活动通过网络药理学分析评估腺肌病治疗

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Background: Sanjie Zhentong capsule (SZC) offers excellent effect in treating adenomyosis (AM), which is a common and difficult gynecological disease in the clinic. However, the systematic analysis of its mechanism has not been carried out yet and further studies are needed to reveal the role of SZC. Methods: A systematic network pharmacology analysis was conducted by integrating construction of SZC compound database and AM target database, prediction of potential active compounds and targets by molecular docking combined with compound-target prediction graph (CTPG), protein-protein interaction (PPI) analysis, Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analysis. Then, the anti–inflammation experiments in vitro were performed by investigating SZC and the representative compounds regulating nitric oxide (NO), interleukin-6 (IL-6), and interleukin-10 (IL-10). Results: Our findings show that SZC mainly treated AM by stimulating 28 core targets through 30 key potential active compounds, and affecting 4 crucial pathways. The treatment was associated with inflammation reaction, hormone regulation, cell adhesion, proliferation, and angiogenesis. Additionally, SZC achieved the anti–inflammatory activity by the cooperation of the compounds through inhibiting NO and IL-6, both promoting and inhibiting IL-10. Conclusion: This study investigated the anti–inflammatory activity of SZC based on a systematic analysis of SZC remedying AM, which was revealed to be one of the essential mechanisms. These findings will provide valuable guidance for further research of the SZC treatment of AM, and help improve the comprehension of SZC pharmacological basis as well as AM pathogenesis.
机译:背景:Sanjie Zhentong胶囊(SZC)在治疗腺细胞症(AM)方面提供出色的效果,这是临床中的常见而困难的妇科疾病。然而,尚未进行其机制的系统分析,并且需要进一步的研究来揭示SZC的作用。方法:通过将SZC复合数据库和AM靶数据库的构建相结合,通过分子对接与复合靶预测图(CTPG),蛋白质 - 蛋白质相互作用(PPI)分析相结合进行系统网络药理学分析,通过分子对接进行潜在的活性化合物和靶标进行预测,基因本体(GO)和京都基因和基因组(KEGG)途径分析。然后,通过研究SZC和调节一氧化氮(NO),白细胞介素-6(IL-6)和白细胞介素-10(IL-10)的代表性化合物进行体外抗炎实验。结果:我们的研究结果表明,SZC主要通过刺激28个核心靶通过30个关键潜在的活性化合物来治疗AM,并影响4个关键途径。该处理与炎症反应,激素调节,细胞粘附,增殖和血管生成有关。另外,SZC通过抑制和抑制IL-10的抑制和IL-6来实现化合物的配合通过化合物的配合实现抗炎活性。结论:本研究研究了SZC的抗炎活性,基于SZC补救措施的系统分析,被揭示为必不可少的机制之一。这些调查结果将为进一步研究AM的SZC治疗提供有价值的指导,并有助于改善SZC药理学基础的理解以及AM发病机制。

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