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运用综合网络药理学方法和分子对接验证以及细胞实验探索古肠止泻丸治疗溃疡性结肠炎的潜在机制。

Exploring the Potential Mechanism of Guchang Zhixie Wan for Treating Ulcerative Colitis by Comprehensive Network Pharmacological Approaches and Molecular Docking Validation as Well as Cell Experiments.

机构信息

Department of Gastroenterology, Second Affiliated Hospital of Traditional Chinese Medicine, No. 5 Weiyang West Road, Xianyang, 712000, P. R. China.

Department of Translational Medicine Center, Second Affiliated Hospital of Traditional Chinese Medicine, No. 5 Weiyang West Road, Xianyang, 712000, P. R. China.

出版信息

Chem Biodivers. 2021 Jan;18(1):e2000810. doi: 10.1002/cbdv.202000810. Epub 2020 Dec 23.

Abstract

Guchang Zhixie Wan (GZW) is a commonly used Chinese medicine for the treatment of ulcerative colitis (UC). This research explored the potential pharmacological mechanism of GZW in UC. The active ingredients, potential targets, and UC-related genes of GZW were retrieved from public databases. The pharmacological mechanisms including key components, potential targets and signal pathways were determined through bioinformatics analysis. The results of this study were verified through virtual molecular docking and cell experiments. Network analysis revealed that 26 active GZW compounds and 148 potential GZW target proteins were associated with UC. Quercetin, kaempferol and β-sitosterol were identified as the core active ingredients of GZW. IFNG, IL-1A, IL-1B, JUN, RELA, and STAT1 were indicated as key targets of GZW. These key targets have a strong affinity for quercetin, kaempferol, and β-sitosterol. GO and KEGG enrichment analysis showed that GZW target proteins are highly enriched in inflammatory, immune, and oxidative stress-related pathways. This study confirmed the therapeutic effect and revealed potential molecular mechanism of GZW on UC. And the protective effects of GZW on inflammatory bowel disease pathway were also revealed through STAT3/NF-κB/IL-6 pathway. The findings of this study enhanced our understanding of GZW in the treatment of UC and provided a feasible method for discovering potential drugs from traditional Chinese medicine formulations.

摘要

固肠止泻丸(GZW)是一种常用于治疗溃疡性结肠炎(UC)的中药。本研究探讨了 GZW 治疗 UC 的潜在药理机制。从公共数据库中检索 GZW 的活性成分、潜在靶点和 UC 相关基因。通过生物信息学分析确定药理机制,包括关键成分、潜在靶点和信号通路。通过虚拟分子对接和细胞实验验证了研究结果。网络分析显示,26 种 GZW 活性化合物和 148 种潜在 GZW 靶蛋白与 UC 相关。槲皮素、山奈酚和β-谷甾醇被确定为 GZW 的核心活性成分。IFNG、IL-1A、IL-1B、JUN、RELA 和 STAT1 被确定为 GZW 的关键靶点。这些关键靶点与槲皮素、山奈酚和β-谷甾醇具有很强的亲和力。GO 和 KEGG 富集分析表明,GZW 靶蛋白在炎症、免疫和氧化应激相关途径中高度富集。本研究证实了 GZW 治疗 UC 的疗效,并揭示了其潜在的分子机制。此外,还通过 STAT3/NF-κB/IL-6 通路揭示了 GZW 对炎症性肠病途径的保护作用。本研究加深了我们对 GZW 治疗 UC 的认识,并为从中药配方中发现潜在药物提供了一种可行的方法。

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