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

被引:16
作者
Du, Li [1 ]
Du, De-Hui [2 ]
Chen, Biao [2 ]
Ding, Yue [3 ]
Zhang, Tong [3 ]
Xiao, Wei [1 ,4 ]
机构
[1] Shanghai Univ Tradit Chinese Med, Inst Chinese Mat Med, Shanghai, Peoples R China
[2] East China Normal Univ, Shanghai Key Lab Trustworthy Comp & Software Engn, Shanghai, Peoples R China
[3] Shanghai Univ Tradit Chinese Med, Expt Ctr Teaching & Learning, 1200 Cailun Rd, Shanghai 201203, Peoples R China
[4] Jiangsu Kanion Pharmaceut Co Ltd, Lianyungang, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
Sanjie Zhentong capsule; adenomyosis; network pharmacology; molecular docking; compound-target prediction graph; anti-inflammation; NF-KAPPA-B; INFLAMMATORY RESPONSE; GINSENOSIDE RH2; HUMAN BREAST; PATHWAY; ENDOMETRIOSIS; EXPRESSION; INHIBITION; ACTIVATION; PATHOGENESIS;
D O I
10.2147/DDDT.S228721
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
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.
引用
收藏
页码:697 / 713
页数:17
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