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基于网络药理学的枳实挥发油治疗慢传输型便秘的作用机制

[Mechanism of Aurantii Fructus Immaturus volatile oil in treatment of slow transit constipation based on network pharmacology].

作者信息

Wang Liang-Feng, Liu Xiao-Li, Li Hui-Ting, Chen Qing-Yao, Wang Yao, Zou Bin, Yang Ming, Zhang Xiao-Fei, Wang Fang

机构信息

Key Laboratory of Modern Preparation of Traditional Chinese Medicine under Ministry of Education, Jiangxi University of Traditional Chinese Medicine Nanchang 330004, China.

School of Pharmacy, Chengdu University of Traditional Chinese Medicine Chengdu 610075, China.

出版信息

Zhongguo Zhong Yao Za Zhi. 2020 Apr;45(8):1909-1917. doi: 10.19540/j.cnki.cjcmm.20200207.302.

Abstract

To construct the active component-action target network diagram and protein-protein interaction(PPI) network diagram of Aurantii Fructus Immaturus volatile oil, so as to explore the mechanism of Aurantii Fructus Immaturus volatile oil in the treatment of slow transit constipation(STC) by analyzing the functions and pathways involved in the target. The chemical constituents of Aurantii Fructus Immaturus volatile oil were determined by gas chromatography-mass spectrometry(GC-MS). The targets of Aurantii Fructus Immaturus volatile oil were studied by PubChem, TCMSP, STITCH and Swiss Target Prediction. OMIM, Genecards-Search Resuits and TTD were used to screen out the targets of Slow Transit Constipation. The active component-action targets and PPI network diagram were constructed by Cytoscape 3.7.1. The target organ distribution was analyzed by BioGPS database. GO and KEGG pathways involved in the targets were analyzed by R language. The molecular docking between the components and the targets was verified by Discovery Studio 2.5 software. Finally, 15 volatile oil compounds from Aurantii Fructus Immaturus were detected, and 115 targets of volatile oil in the treatment of STC were predicted. GO enrichment analysis showed that the activity of Aurantii Fructus Immaturus volatile oil mainly involved blood circulation, circulation system process, response to steroid hormone, signal release and other biological processes. There were 23 KEGG enrichment pathways, among which Neuroactive ligand-receptor interaction, cAMP signaling pathway, Endocrine resistance, Calcium signaling pathway and Serotonergic synapse pathways played a significant role in STC. The results of molecular docking showed that relevant target proteins for the treatment of STC were ACHE, PTGS2, SLC6 A2 and CNR2.The multi-component, multi-target and multi-pathwaycharacteristics of Aurantii Fructus Immaturus volatile oil were revealed by network pharmacology, which provided a new therapeutic idea and method for the further study of the mechanism of Aurantii Fructus Immaturus volatile oil in the treatment of STC.

摘要

构建青皮挥发油的活性成分-作用靶点网络图和蛋白质-蛋白质相互作用(PPI)网络图,通过分析靶点所涉及的功能和通路,探讨青皮挥发油治疗慢传输型便秘(STC)的作用机制。采用气相色谱-质谱联用(GC-MS)法测定青皮挥发油的化学成分。通过PubChem、TCMSP、STITCH和瑞士靶点预测软件研究青皮挥发油的靶点。利用OMIM、Genecards搜索结果和TTD筛选慢传输型便秘的靶点。运用Cytoscape 3.7.1构建活性成分-作用靶点和PPI网络图。通过BioGPS数据库分析靶点的器官分布。运用R语言分析靶点所涉及的GO和KEGG通路。利用Discovery Studio 2.5软件验证成分与靶点之间的分子对接。最终,检测出青皮中的15种挥发油化合物,预测出115个挥发油治疗STC的靶点。GO富集分析表明,青皮挥发油的活性主要涉及血液循环、循环系统过程、对类固醇激素的反应、信号释放等生物学过程。KEGG富集通路有23条,其中神经活性配体-受体相互作用、cAMP信号通路、内分泌抵抗、钙信号通路和5-羟色胺能突触通路在STC中起重要作用。分子对接结果显示,治疗STC的相关靶蛋白为ACHE、PTGS2、SLC6A2和CNR2。网络药理学揭示了青皮挥发油多成分、多靶点、多通路的特点,为进一步研究青皮挥发油治疗STC的作用机制提供了新的治疗思路和方法。

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