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基于系统药理学的方法探究喜杷匏溃结安灌肠方治疗溃疡性结肠炎的活性成分及作用机制。

A Systems Pharmacology Approach to Determine Active Compounds and Action Mechanisms of Xipayi KuiJie'an enema for Treatment of Ulcerative colitis.

机构信息

School of Pharmacy, Xinjiang Shihezi University, Xinjiang, 832002, China.

Key Laboratory of Chinese Internal Medicine of Education, DongZhiMen Hospital, Beijing, 100070, China.

出版信息

Sci Rep. 2017 Apr 26;7(1):1189. doi: 10.1038/s41598-017-01335-w.

DOI:10.1038/s41598-017-01335-w
PMID:28446747
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5430631/
Abstract

Xipayi Kui Jie'an (KJA), a type of traditional Uygur medicine (TUM), has shown promising therapeutic effects in Ulcerative colitis (UC). Owing to the complexity of TUM, the pharmacological mechanism of KJA remains vague. Therefore, the identification of complex molecular mechanisms is a major challenge and a new method is urgently needed to address this problem. In this study, we established a feasible pharmacological model based on systems pharmacology to identify potential compounds and targets. We also applied compound-target and target-diseases network analysis to evaluate the action mechanisms. According to the predicted results, 12 active compounds were selected and these compounds were also identified by HPLC-ESI-MS/MS analysis. The main components were tannins, this result is consistent with the prediction. The active compounds interacted with 22 targets. Two targets including PTGS2 and PPARG were demonstrated to be the main targets associated with UC. Systematic analysis of the constructed networks revealed that these targets were mainly involved in NF-κB signaling pathway. Furthermore, KJA could also regulate the CD4 + CD25 + Foxp3 + Treg cells. In conclusion, this systems pharmacology-based approach not only explained that KJA could alleviate the UC by regulating its candidate targets, but also gave new insights into the potential novel therapeutic strategies for UC.

摘要

西帕依溃结安(KJA),一种维吾尔药(TUM),在溃疡性结肠炎(UC)中显示出有希望的治疗效果。由于 TUM 的复杂性,KJA 的药理机制仍不清楚。因此,鉴定复杂的分子机制是一个主要的挑战,需要一种新的方法来解决这个问题。在本研究中,我们建立了一个基于系统药理学的可行的药理学模型,以鉴定潜在的化合物和靶点。我们还应用了化合物-靶点和靶点-疾病网络分析来评估作用机制。根据预测结果,选择了 12 种活性化合物,并用 HPLC-ESI-MS/MS 分析对这些化合物进行了鉴定。主要成分是单宁,这一结果与预测一致。活性化合物与 22 个靶点相互作用。两个靶点,包括 PTGS2 和 PPARG,被证明是与 UC 相关的主要靶点。对构建网络的系统分析表明,这些靶点主要参与 NF-κB 信号通路。此外,KJA 还可以调节 CD4+CD25+Foxp3+Treg 细胞。总之,这种基于系统药理学的方法不仅解释了 KJA 可以通过调节其候选靶点来缓解 UC,而且为 UC 的潜在新治疗策略提供了新的见解。

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