Mechanism of pruritus ani lotion combined with Huajiao-Gancao-Bingpian oil for pruritus ani treatment based on network pharmacology and molecular dynamics.

IF 1.4 4区 医学 Q3 ALLERGY
Postepy Dermatologii I Alergologii Pub Date : 2024-04-01 Epub Date: 2024-04-25 DOI:10.5114/ada.2023.135761
Wenkuo Deng, Minghong Fu, Jintao Huang
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引用次数: 0

Abstract

Introduction: Pruritus ani lotion combined with a Chinese medicine formula named Huajiao (Pericarpium Zanthoxyli Bungeani)-Gancao (Radix Glycyrrhizae)-Bingpian (Borneol) is effective in treating pruritus ani.

Aim: To investigate the mechanism of traditional Chinese medicine (TCM) in pruritus ani via network pharmacology and molecular dynamics (MD).

Material and methods: The Traditional Chinese Medicine Systems Pharmacology Database and Analysis Platform (TCMSP) was utilised to screen active ingredients and their corresponding targets. Genes associated with pruritus ani were collected through GeneCards. Protein-protein interaction (PPI) network between target genes of the active ingredients of this formula and genes associated with pruritus ani was established through the STRING database. A drug-active ingredient-gene interaction network was constructed using Cytoscape with the top 50 genes in affinity coefficients. Molecular docking and MD simulation analysis were performed.

Results: Epidermal growth factor receptor (EGFR) and Signal Transducer and Activator of Transcription 3 (STAT3) were core genes. Direct targeting of EGFR by the active ingredients (quercetin and luteolin) and direct targeting of STAT3 by the active ingredient (licochalcone A) may be key molecular mechanisms for the treatment of pruritus ani. Simulated trajectories of structural nuclear motion by MD also revealed that the binding of two pairs of molecules was relatively stable.

Conclusions: This study unravels potential targets, active ingredients, and mechanisms of pruritus ani lotion combined with Huajiao-Gancao-Bingpian oil in the treatment of pruritus ani, providing a reference for future treatment.

基于网络药理学和分子动力学的肛门瘙痒症洗剂联合花椒-甘草-冰片油治疗肛门瘙痒症的机理。
简介目的:通过网络药理学和分子动力学(MD)研究中药治疗皮肤瘙痒症的机制:利用中药系统药理学数据库和分析平台(TCMSP)筛选有效成分及其相应靶点。通过 GeneCards 收集与肛门瘙痒症相关的基因。通过 STRING 数据库建立了本方有效成分靶基因与肛门瘙痒症相关基因之间的蛋白-蛋白相互作用(PPI)网络。使用 Cytoscape 构建了药物活性成分-基因相互作用网络,其中包括亲和力系数排名前 50 位的基因。进行了分子对接和 MD 模拟分析:结果:表皮生长因子受体(EGFR)和信号转导及转录激活因子 3(STAT3)是核心基因。有效成分(槲皮素和木犀草素)对表皮生长因子受体的直接靶向作用和有效成分(甘草查耳酮 A)对 STAT3 的直接靶向作用可能是治疗皮肤瘙痒症的关键分子机制。MD 模拟的结构核运动轨迹还显示,两对分子的结合相对稳定:本研究揭示了花椒甘草冰片油联合肛门瘙痒洗剂治疗肛门瘙痒症的潜在靶点、有效成分和作用机制,为今后的治疗提供了参考。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
2.60
自引率
7.10%
发文量
107
审稿时长
6-12 weeks
期刊介绍: Advances in Dermatology and Allergology/Postępy Dermatologii i Alergologii is a bimonthly aimed at allergologists and dermatologists.
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