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基于网络药理学预测参茱连柏汤治疗溃疡性结肠炎作用机制。

Network pharmacological prediction of the mechanism of action of Shen-Zhu-Lian-Bai Decoction in the treatment of ulcerative colitis.

机构信息

Anorectal Surgery, Shenzhen TCM Anorectal Hospital, Shenzhen, Guangdong, China.

Anorectal Surgery, Meizhou People's Hospital, Meizhou, Guangdong, China.

出版信息

Sci Rep. 2024 Jun 20;14(1):14183. doi: 10.1038/s41598-024-64683-4.

Abstract

The incidence of ulcerative colitis (UC) is on the rise globally. Shen-Zhu-Lian-Bai decoction (SZLBD) can relieve the clinical symptoms of UC. This study aimed to investigate the underlying molecular mechanism of SZLBD in the treatment of UC. The key treatment targets of SZLBD for UC were obtained based on the online database, and combined with the STRING database and Cytoscape 3.7.2 software, PPI network was constructed and visualized. The GEO database was utilized to validate the expression levels of core targets in UC. Metascape database GO functional annotation and KEGG pathway enrichment analysis. Molecular docking technology was used to verify the docking of core compounds with key targets. RT-qPCR and Western Blot were used to detect the expression of key targets in HCoEpiC cells for verification. After screening, 67 targets shared by SZLBD and UC were obtained. It is predicted that IL-6, IL-1B, and AKT1 might be the key targets of SZLBD in the treatment of UC. Quercetin was the main active ingredient. GEO results showed that the expression levels of IL-6, IL-1B and AKT1 were higher in the UC group compared to the control group. GO and KEGG analyses showed that these targets were related to apoptosis and inflammation. The results of molecular docking demonstrated that the AKT1 gene, a key target of quercetin, had the highest affinity of -9.2 kcal/mol. Cell experiments found that quercetin could affect the expression of IL-6, IL-1B, and AKT1. This study preliminarily explored and verified the mechanism of action of SZLBD in the treatment of UC, which provides a theoretical basis for subsequent in vivo mechanism studies.

摘要

溃疡性结肠炎(UC)的发病率在全球呈上升趋势。参茱连柏汤(SZLBD)可缓解 UC 的临床症状。本研究旨在探讨 SZLBD 治疗 UC 的潜在分子机制。基于在线数据库获得 SZLBD 治疗 UC 的关键治疗靶点,并结合 STRING 数据库和 Cytoscape 3.7.2 软件构建和可视化 PPI 网络。利用 GEO 数据库验证 UC 中核心靶点的表达水平。Metascape 数据库进行 GO 功能注释和 KEGG 通路富集分析。采用分子对接技术验证核心化合物与关键靶点的对接。使用 RT-qPCR 和 Western blot 检测 HCoEpiC 细胞中关键靶点的表达进行验证。筛选后,获得 SZLBD 和 UC 共有的 67 个靶点。预测 IL-6、IL-1B 和 AKT1 可能是 SZLBD 治疗 UC 的关键靶点。槲皮素是主要的活性成分。GEO 结果表明,UC 组中 IL-6、IL-1B 和 AKT1 的表达水平高于对照组。GO 和 KEGG 分析表明,这些靶点与细胞凋亡和炎症有关。分子对接结果表明,槲皮素的关键靶点 AKT1 基因具有最高的亲和力为-9.2 kcal/mol。细胞实验发现,槲皮素可影响 IL-6、IL-1B 和 AKT1 的表达。本研究初步探讨和验证了 SZLBD 治疗 UC 的作用机制,为后续体内机制研究提供了理论依据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9bab/11190269/87b08dd24063/41598_2024_64683_Fig1_HTML.jpg

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