Network pharmacology-based prediction for therapeutic mechanism of FuYueKang Lotion on acute eczema

Xiaowen Wen, Shaokang Cui, Minzhi Li, Yongping Zheng, Haoyou Xu
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Abstract

Objective: Fuyuekang Lotion (FYKL) is an improved traditional Chinese medicine (TCM) prescription widely used to treat acute eczema (AE). However, the mechanism of action remains unclear. This study aimed to explore the therapeutic mechanism of FYKL in AE.Methods: We revealed the underlying mechanism by utilizing a network pharmacology approach, molecular docking studies, and in vitro verification. The active compounds in FYKL were identified, and their targets were predicted. These targets were subsequently mapped to a component-target interaction network, with their therapeutic mechanisms predicted through Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) enrichment analyses. Molecular docking was used to verify protein-binding efficacy. Potential key targets of FYKL against AE were further confirmed via reverse transcription quantitative polymerase chain reaction (RT-qPCR).Results: The study identified 59 potential active compounds of FYKL, with quercetin, luteolin, and gallic acid suggested as critical active ingredients. Our findings suggest that these ingredients could exert their effects mainly by modulating the inflammatory immune response and promoting epidermal repair. FYKL was found to be a multi-target, multi-component drug that could potentially regulate the inflammatory immune response in AE through numerous pathways.Conclusions: The findings from this study provide a scientific basis for further research into the therapeutic effects and mechanisms of FYKL in treating AE, underscoring the potential of TCM in modern therapeutics.
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基于网络药理学的妇月康洗剂治疗急性湿疹机理预测
目的:妇月康洗剂是一种被广泛应用于治疗急性湿疹(AE)的中药改良方。然而,其作用机制尚不清楚。本研究旨在探讨FYKL治疗AE的作用机制。方法:利用网络药理学方法、分子对接研究和体外验证来揭示其潜在机制。鉴定了FYKL中的活性化合物,并对其靶点进行了预测。这些靶标随后被映射到一个组件-靶标相互作用网络,并通过基因本体(GO)和京都基因与基因组百科全书(KEGG)富集分析预测了它们的治疗机制。通过分子对接验证蛋白结合效果。通过反转录定量聚合酶链反应(RT-qPCR)进一步确定FYKL抗AE的潜在关键靶点。结果:鉴定出59种潜在活性成分,其中槲皮素、木犀草素、没食子酸为关键活性成分。我们的研究结果表明,这些成分可能主要通过调节炎症免疫反应和促进表皮修复来发挥作用。我们发现FYKL是一种多靶点、多组分的药物,可能通过多种途径调节AE的炎症免疫反应。结论:本研究结果为进一步研究FYKL治疗AE的疗效和机制提供了科学依据,凸显了中医药在现代治疗中的潜力。
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