三黄治疗痤疮的网络药理学分析及实验研究

Ju PENG , Yan WANG , Zhancao LI , Xi LUO , Jun SHI , Limin ZHAO , Ping ZHAO
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引用次数: 0

摘要

目的基于网络药理学和分子对接技术,探索“三黄泻心汤”(简称“三黄”)抗痤疮的主要有效成分和潜在靶点,并通过生化实验研究其抑菌机制。方法采用药理学数据库、中药系统分析平台(TCMSP)数据库和SwissTarget数据库,分别获取三黄治疗痤疮的有效成分和靶点。通过OMIM、GeneCards和DisGeNET数据库筛选与痤痘相关的靶点,通过Cytoscape和String数据库分析相互作用靶点,然后通过Genome Encyclopedia (KEGG)和Gene Ontology (GO)进行富集分析。通过分子对接验证了预测结果。采用牛津杯法确定三黄对痤疮的抑菌带,采用双倍稀释法获得最小抑菌浓度。通过扫描电镜观察三黄存在下细菌形态的变化,检测离子泄漏率,反映细菌细胞壁的通透性。最后,检测药物治疗后痤疮组织中IL-6的表达。结果从掌大黄、黄连、黄芩中分别筛选出34、25、44个有效成分,筛选出145、216、163个复方靶点。三黄与痤疮有123个交叉靶点,主要通过IL-17、MAPK、PI3K-Akt、TNF等信号通路起作用。分子模拟结果显示,黄连中的芦荟大黄素和槲皮素与TNF、IL-6、INS、AKT1等核心靶点具有较强的亲和性。三黄在0.1 g/mL和0.5 g/mL浓度下的抑菌带分别为(21.0±0.3)mm和(26.1±0.9)mm,呈明显的剂量依赖关系。三黄最低抑菌浓度为4 mg/mL。此外,在药物治疗的痤疮中,细菌细胞的形态被破坏,细胞壁的通透性增加,痤疮丙酸杆菌的生长受到抑制。细胞实验结果显示,三黄对IL-6的表达有抑制作用。结论基于网络药理学方法,预测了三黄治疗痤疮多组分、多靶点、多通路的作用机制,并通过抑菌试验、细胞实验等生化方法验证了三黄对痤疮的治疗效果。三黄主要通过调节TNF、IL-6、INS、AKT1等靶基因抑制痤疮丙酸杆菌的生长。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Analysis on the treatment of acne by Sanhuang with network pharmacology and experimental research

Objective

To explore the main active components and potential targets of “Sanhuang Xiexin decoction” (Sanhuang) against acne based on network pharmacology and molecular docking technology, and research the bacteriostatic mechanism by biochemical experiments.

Methods

Pharmacological database and Analysis platform of the Traditional Chinese Medicine System (TCMSP) and SwissTarget database were used to obtain the active components and the targets of Sanhuang in the treatment of acne, respectively. The acne-related targets were screened by OMIM, GeneCards, and DisGeNET databases, and the interaction targets were analyzed by Cytoscape and String databases, followed with enrichment analysis by Genome Encyclopedia (KEGG) and Gene Ontology (GO). The predicted results were validated by molecular docking. The bacteriostatic zones of Sanhuang to acne were determined by Oxford cup method, and the minimum bacteriostasis concentration was obtained by double dilution method. The bacteria morphology change in the presence of Sanhuang was observed by scanning electron microscope and the ionic leakage rate was detected to reflect the permeability of bacterial cell walls. Finally, the IL-6 expression of drug-treated acne was determined.

Results

From Rheum palmatum L, Coptis chinensis Franch, and Scutellaria baicalensis Georgi, 34, 25 and 44 active ingredients were selected, and 145, 216 and 163 compound targets were screened out, respectively. There are 123 intersection targets of Sanhuang and acne, which mainly function through IL-17, MAPK, PI3K-Akt, and TNF signaling pathways. Molecular simulation results showed that aloe-emodin and quercetin in Coptis Chinensis Franch had strong affinities with the core targets of TNF, IL-6, INS, and AKT1. The antibacterial zones of Sanhuang at concentrations of 0.1 g/mL and 0.5 g/mL were (21.0±0.3) mm and (26.1±0.9) mm, respectively, which had an obvious dose-dependent relationship. The minimum inhibitory concentration of Sanhuang was 4 mg/mL. Moreover, in the drug-treated acne, the morphology of bacterial cells was destroyed, the permeability of cell walls was increased, and the growth of propionibacterium acnes was inhibited. The results of cell experiment showed that Sanhuang inhibited the expression of IL-6.

Conclusion

Based on network pharmacology method, we predicted the mechanism of Sanhuang in the treatment of acne which was charactered by multi-component, multi-target, and multi-pathway, and verified the therapeutic effect of Sanhuang on acne by the biochemical method such as bacteriostasis test and cell experiment. Sanhuang can inhibit the growth of Propionibacterium acnes mainly by regulating the target genes such as TNF, IL-6, INS, and AKT1.

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