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基于网络药理学探讨左金丸治疗溃疡性结肠炎的潜在生物活性成分及作用机制

Based on Network Pharmacology to Explore the Potential Bioactive Compounds and Mechanisms of Zuojin Pill for the Treatment of Ulcerative Colitis.

作者信息

Wei Ying, Ren Sichen, Wang Ruilin, Jing Manyi, Liu Honghong, Wang Min, Song Hongtao, Zhao Yanling

机构信息

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

Department of Pharmacy, The Fifth Medical Center of Chinese PLA General Hospital, Beijing, China.

出版信息

Evid Based Complement Alternat Med. 2021 Aug 26;2021:7567025. doi: 10.1155/2021/7567025. eCollection 2021.

Abstract

BACKGROUND

Zuojin Pill (ZJP), a classic prescription, has the potential to prevent ulcerative colitis (UC). However, the active components and mechanisms of ZJP are still arcane. This study aimed to use a network pharmacology approach to find the bioactive compounds and potential action mechanisms of ZJP in the treatment of UC.

METHODS

Firstly, the components and putative targets of ZJP were collected based on herbal medicine target databases, and a network containing the interaction between the targets of ZJP and the potential therapeutic targets of UC was established. Then, topological parameters were calculated to identify the key targets in the network and, in turn, to import them into the David database to perform path enrichment analysis.

RESULTS

14 potential therapeutic components of ZJP and 26 key targets were obtained. These targets were related to signal transduction, MAPK cascade, inflammatory response, immune response, and the apoptotic process of UC. Moreover, the PI3K-Akt signaling pathway, MAPK signaling pathway, toll-like receptor signaling pathway, and Prolactin signaling pathway were predicted to participate in ZJP treating UC. Among them, 14 active components of ZJP directly regulate these pathways.

CONCLUSION

ZJP could alleviate UC through the predicted components and mechanisms. The 14 predicted active components of ZJP may mainly play a therapeutic role for UC through synergistic regulation of the PI3K-Akt signaling pathway and MAPK signaling pathway.

摘要

背景

左金丸(ZJP)作为经典方剂,具有预防溃疡性结肠炎(UC)的潜力。然而,左金丸的活性成分和作用机制仍不清楚。本研究旨在采用网络药理学方法,探寻左金丸治疗UC的生物活性化合物及潜在作用机制。

方法

首先,基于草药靶点数据库收集左金丸的成分和假定靶点,构建左金丸靶点与UC潜在治疗靶点相互作用的网络。然后,计算拓扑参数以识别网络中的关键靶点,进而将其导入David数据库进行通路富集分析。

结果

获得了左金丸14种潜在治疗成分和26个关键靶点。这些靶点与UC的信号转导、丝裂原活化蛋白激酶(MAPK)级联反应、炎症反应、免疫反应及凋亡过程相关。此外,预测PI3K-Akt信号通路、MAPK信号通路、Toll样受体信号通路和催乳素信号通路参与左金丸治疗UC的过程。其中,左金丸的14种活性成分直接调控这些通路。

结论

左金丸可通过预测的成分和机制缓解UC。左金丸预测的14种活性成分可能主要通过协同调控PI3K-Akt信号通路和MAPK信号通路对UC发挥治疗作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2401/8416371/54cf1a0ab5e7/ECAM2021-7567025.001.jpg

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