柴煊, 孟雅坤, 柏兆方, 张雅铭, 肖小河, 牛明. 基于生物靶标网络分析的山豆根抗乙肝病毒的作用机制初步研究J. 药学学报, 2018,53(3): 396-402. doi: 10.16438/j.0513-4870.2017-1124
引用本文: 柴煊, 孟雅坤, 柏兆方, 张雅铭, 肖小河, 牛明. 基于生物靶标网络分析的山豆根抗乙肝病毒的作用机制初步研究J. 药学学报, 2018,53(3): 396-402. doi: 10.16438/j.0513-4870.2017-1124
CHAI Xuan, MENG Ya-kun, BAI Zhao-fang, ZHANG Ya-ming, XIAO Xiao-he, NIU Ming. Mechanism of anti-hepatitis B virus activity of Tonkinensis based on biological targets networkJ. Acta Pharmaceutica Sinica, 2018,53(3): 396-402. doi: 10.16438/j.0513-4870.2017-1124
Citation: CHAI Xuan, MENG Ya-kun, BAI Zhao-fang, ZHANG Ya-ming, XIAO Xiao-he, NIU Ming. Mechanism of anti-hepatitis B virus activity of Tonkinensis based on biological targets networkJ. Acta Pharmaceutica Sinica, 2018,53(3): 396-402. doi: 10.16438/j.0513-4870.2017-1124

基于生物靶标网络分析的山豆根抗乙肝病毒的作用机制初步研究

Mechanism of anti-hepatitis B virus activity of Tonkinensis based on biological targets network

  • 摘要: 山豆根是一味常用于治疗乙肝的中药,在改善症状、保肝降酶、利胆退黄等方面疗效确切,但其抗乙肝病毒的作用机制尚不明确。为此,本文基于系统生物学的思想,通过整合网络药理学与代谢组学两种技术,较为系统地分析山豆根抗病毒的主要作用机制。首先,通过预测山豆根中主要化学成分的作用靶标,建立山豆根的“药物成分-靶标”网络;其次,以人肝癌细胞HepG2.2.15为研究对象,通过代谢组学技术分析山豆根抗乙肝的主要代谢过程和其主要影响的代谢物;最后,通过构建“药物成分-靶标-代谢物”网络,分析山豆根抗乙肝的主要作用靶标及代谢物,进而阐明其主要作用机制。山豆根可能主要作用于16个靶标蛋白发挥抗乙肝病毒作用,其作用机制可能与调节视黄醇代谢、过氧化物酶体增殖物激活型受体(peroxisome proliferator activate-receptors,PPAR)信号通路、癌症中的转录失调等过程有关,从而达到控制乙肝病毒复制、调节机体免疫和代谢功能紊乱等作用。

     

    Abstract: Tonkinensis is commonly used in the treatment of hepatitis B infection in China with its effect­tiveness in reducing clinical symptoms and improving liver function. However, the mechanism of the anti-HBV (hepatitis B virus) effect of Tonkinensis is still not clear. In this study, an integrative analysis using the network pharmacology and metabolomics was employed in identification of the main targets and mechanisms of Tonkinensis in treatment of HBV infections. First, the "drug-target" network was established by predicting the targets of the main chemical components of Tonkinensis; Secondly, the differential metabolites associated with the anti-HBV effect of Tonkinensis were analyzed with the LC-MS based metabolomics in HepG2.2.15 cells; Finally, the "drug ingredients-targets-metabolites" network was constructed to screen the main anti-HBV targets of Tonkinensis. The results suggest that Tonkinensis may act on 16 target proteins in the network of retinol metabolism, peroxisome proliferator activate-receptors (PPAR) signaling pathway and transcriptional regulation of cancer and so on, which contributed to the control of HBV replication and the regulation of immune function and metabolic disorders.

     

/

返回文章
返回