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左清散保留灌肠治疗乙状结肠溃疡性结肠炎的有效成分及作用机制。

The active ingredients and mechanism of Zuoqing San in the treatment of sigmoid ulcerative colitis by retention enema.

作者信息

Li Ming, Deng Heng, Xu Shuqing, Fang Xiaoli, Tang Kun, Chen Li, Zha Ansheng

机构信息

Department of Anorectal Surgery, 117843 The First Affiliated Hospital of Anhui University of Chinese Medicine , Hefei, China.

Department of Anorectal Surgery, 117843 The Second Affiliated Hospital of Anhui University of Chinese Medicine , Hefei, China.

出版信息

J Complement Integr Med. 2025 Feb 24;22(2):343-352. doi: 10.1515/jcim-2024-0435. eCollection 2025 Jun 1.

Abstract

OBJECTIVES

This investigation aimed to evaluate the efficacy, key active ingredients, and mechanisms of Zuoqing San (ZQS), a traditional Chinese medicine formula, in managing sigmoid ulcerative colitis (SUC).

METHODS

A cohort of 126 participants was recruited and treated with ZQS at a daily dosage of 100 mL for 12 weeks. The primary endpoint was the percentage of subjects achieving favorable treatment outcomes. Liquid chromatography-mass spectrometry was employed to identify the principal ingredients of ZQS. Network pharmacology was utilized to predict the central targets of its active ingredients. Protein-protein interaction networks, Gene Ontology enrichment analyses, and Kyoto Encyclopedia of Genes and Genomes pathway analyses were conducted for identified core targets. Finally, molecular dynamics simulations of key active ingredients and core targets were performed.

RESULTS

Following 12 weeks of therapy, with a withdrawal rate of 7.93 %, favorable treatment outcomes were observed in 31.03 % of subjects at 4 weeks, 66.37 % at 8 weeks (Odds Ratio: 1.54, 95 % Confidence Interval: 0.41-1.83), and 68.10 % at 12 weeks (Odds Ratio: 1.86, 95 % CI: 0.32-1.27). ZQS comprises 31 principal chemical constituents. Key targets within the protein-protein interaction network included TNF, AKT1, IL6, IL1β, PTGS2, TP53, JUN, MMP9, CASP3, HIF1A, and BCL1. Pathway analysis indicated ZQS primarily impacts the TNF, NF-kB, and IL-17 signaling pathways. Molecular dynamics simulation results showed oxymatrine, cynarin had higher affinity with TNF and IL1β, respectively.

CONCLUSIONS

This research elucidates the active components of ZQS and its potential multicomponent-multitarget-multipathway pharmacological mechanisms, demonstrating promising therapeutic potential for SUC management.

摘要

目的

本研究旨在评估中药方剂左金散(ZQS)治疗乙状结肠溃疡性结肠炎(SUC)的疗效、关键活性成分及作用机制。

方法

招募126名参与者,给予ZQS每日剂量100 mL,治疗12周。主要终点是达到良好治疗效果的受试者百分比。采用液相色谱 - 质谱法鉴定ZQS的主要成分。利用网络药理学预测其活性成分的核心靶点。对鉴定出的核心靶点进行蛋白质 - 蛋白质相互作用网络、基因本体富集分析和京都基因与基因组百科全书通路分析。最后,对关键活性成分和核心靶点进行分子动力学模拟。

结果

治疗12周后,脱落率为7.93%,4周时31.03%的受试者达到良好治疗效果,8周时为66.37%(优势比:1.54,95%置信区间:0.41 - 1.83),12周时为68.10%(优势比:1.86,95%CI:0.32 - 1.27)。ZQS包含31种主要化学成分。蛋白质 - 蛋白质相互作用网络中的关键靶点包括TNF、AKT1、IL6、IL1β、PTGS2、TP53、JUN、MMP9、CASP3、HIF1A和BCL1。通路分析表明ZQS主要影响TNF、NF - kB和IL - 17信号通路。分子动力学模拟结果显示氧化苦参碱、绿原酸分别与TNF和IL1β具有较高亲和力。

结论

本研究阐明了ZQS的活性成分及其潜在的多成分 - 多靶点 - 多途径药理机制,显示出在SUC治疗方面具有良好的治疗潜力。

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