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基于网络药理学和分子对接的黄连解毒汤治疗溃疡性结肠炎的分子机制。

Molecular mechanisms of Huanglian jiedu decoction on ulcerative colitis based on network pharmacology and molecular docking.

机构信息

Department of Gastroenterology, The First Affiliated Hospital of Nanchang University, 17 Yongwaizheng Street, Nanchang, 330006, Jiangxi, China.

出版信息

Sci Rep. 2022 Apr 1;12(1):5526. doi: 10.1038/s41598-022-09559-1.

Abstract

Huanglian jiedu decoction (HLJDD) is a heat-clearing and detoxifying agent composed of four kinds of Chinese herbal medicine. Previous studies have shown that HLJDD can improve the inflammatory response of ulcerative colitis (UC) and maintain intestinal barrier function. However, its molecular mechanism is not completely clear. In this study, we verified the bioactive components (BCI) and potential targets of HLJDD in the treatment of UC using network pharmacology and molecular docking, and constructed the pharmacological network and PPI network. Then the core genes were enriched by GO and KEGG. Finally, the bioactive components were docked with the key targets to verify the binding ability between them. A total of 54 active components related to UC were identified. Ten genes are very important to the PPI network. Functional analysis showed that these target genes were mainly involved in the regulation of cell response to different stimuli, IL-17 signal pathway and TNF signal pathway. The results of molecular docking showed that the active components of HLJDD had a good binding ability with the Hub gene. This study systematically elucidates the "multi-component, multi-target, multi-pathway" mechanism of anti-UC with HLJDD for the first time, suggesting that HLJDD or its active components may be candidate drugs for the treatment of ulcerative colitis.

摘要

黄连解毒汤(HLJDD)是由四种中草药组成的清热解毒剂。先前的研究表明,HLJDD 可以改善溃疡性结肠炎(UC)的炎症反应并维持肠道屏障功能。然而,其分子机制尚不完全清楚。在这项研究中,我们使用网络药理学和分子对接技术验证了 HLJDD 在治疗 UC 中的生物活性成分(BCI)和潜在靶点,并构建了药理学网络和 PPI 网络。然后通过 GO 和 KEGG 对核心基因进行富集。最后,将生物活性成分与关键靶点对接,验证它们之间的结合能力。共鉴定出 54 种与 UC 相关的活性成分。十个基因对 PPI 网络非常重要。功能分析表明,这些靶基因主要参与细胞对不同刺激的反应、IL-17 信号通路和 TNF 信号通路的调节。分子对接结果表明,HLJDD 的活性成分与枢纽基因具有良好的结合能力。这项研究首次系统地阐明了 HLJDD 抗 UC 的“多成分、多靶点、多途径”机制,提示 HLJDD 或其活性成分可能是治疗溃疡性结肠炎的候选药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4101/8975855/5c2c2599b840/41598_2022_9559_Fig1_HTML.jpg

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