韩彦琪, 许浚, 张喜民, 张铁军, 任一杰, 刘昌孝. 基于网络药理学的元胡止痛滴丸治疗原发性痛经的作用机制研究J. 药学学报, 2016,51(3): 380-387. doi: 10.16438/j.0513-4870.2015-0550
引用本文: 韩彦琪, 许浚, 张喜民, 张铁军, 任一杰, 刘昌孝. 基于网络药理学的元胡止痛滴丸治疗原发性痛经的作用机制研究J. 药学学报, 2016,51(3): 380-387. doi: 10.16438/j.0513-4870.2015-0550
HAN Yan-qi, XU Jun, ZHANG Xi-min, ZHANG Tie-jun, REN Yi-jie, LIU Chang-xiao. Network pharmacology-based study on mechanism of Yuanhu Zhitong Dropping Pills in the treatment of primary dysmenorrheaJ. Acta Pharmaceutica Sinica, 2016,51(3): 380-387. doi: 10.16438/j.0513-4870.2015-0550
Citation: HAN Yan-qi, XU Jun, ZHANG Xi-min, ZHANG Tie-jun, REN Yi-jie, LIU Chang-xiao. Network pharmacology-based study on mechanism of Yuanhu Zhitong Dropping Pills in the treatment of primary dysmenorrheaJ. Acta Pharmaceutica Sinica, 2016,51(3): 380-387. doi: 10.16438/j.0513-4870.2015-0550

基于网络药理学的元胡止痛滴丸治疗原发性痛经的作用机制研究

Network pharmacology-based study on mechanism of Yuanhu Zhitong Dropping Pills in the treatment of primary dysmenorrhea

  • 摘要: 探究元胡止痛滴丸治疗原发性痛经的多成分、多靶点、多途径作用机制,建立其"化合物-靶点-通路-疾病"的网络药理研究模式。针对元胡止痛滴丸中28个入血成分(22个原型化合物及6个代谢产物),利用PharmMapper服务器建立化合物-靶蛋白网络,通过Kyoto Encyclopedia of Genes and Genomes (KEGG)数据库对获取的靶点进行相关通路分析,最后利用Cytoscape软件构建元胡止痛滴丸的"化合物-靶点-通路-疾病"网络图。预测实验表明, 28个入血成分的作用靶点约为109个,共涉及通路111条,其中52个靶点蛋白和31条通路与原发性痛经相关。元胡止痛滴丸可能通过作用于和激素调节、中枢镇痛、解痉、炎症及免疫相关的蛋白靶点及通路,起到治疗原发性痛经的作用。

     

    Abstract: This study was designed to explore the mechanism of Yuanhu Zhitong Dropping Pills (YHZT) in the treatment of primary dysmenorrhea by pharmacological network technology and establish a research approach of "Compound-Target-Pathway-Disease" network. Twenty-eight compounds absorbed into blood including 22 prototype and 6 metabolites of YHZT were submitted to PharmMapper and Kyoto Encyclopedia of Genes and Genomes (KEGG) bioinformatics softwares to predict the target proteins and related pathways respectively. The network of "Compound-Target-Pathway-Disease" was constructed and analyzed using Cytoscape software. The in silico prediction results showed that the 28 constituents of YHZT affected 111 pathways through 109 target proteins. Among them, a total of 52 proteins and 31 pathways were related to the primary dysmenorrhea. The effect of YHZT on primary dysmenorrhea may be dependent on regulation of the proteins and pathways related with hormonal regulation, central analgesia, spasmolysis, inflammation and immunoregulation.

     

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