Demonstrates the therapeutic mechanisms of baicalein in atopic dermatitis, indicating its potential as a treatment.
This study aims to explore the therapeutic mechanisms of baicalein, a flavonoid from Wudang Mountain Scutellaria baicalensis Georgi., in treating atopic dermatitis (AD) using a combination of network pharmacology, transcriptomics, molecular docking, and in vitro experiments. Based on the UPLC-MS/MS analysis, 271 compounds including 10 categories were identified, with flavonoids (62.36%) being the most abundant. Network pharmacology revealed 21 intersection targets between baicalein and AD, and PPI network analysis identified 10 hub genes, including MMP9, MAPK3, EGFR, TLR4, etc. Skin RNA-sequencing from normal and AD mice confirmed 9 of the 21 common targets, and KEGG enrichment analysis highlighted HIF-1α signalling pathway as the key mechanism. In silico molecular docking proved that baicalein has strong binding affinity with TLR4, EGFR, and VEGFA, which were the core targets enriched in HIF-1α signalling pathway. Additionally, in vitro cell experiments demonstrated that baicalein significantly down-regulated the protein expression levels of HIF-1α, TLR4, VEGFA.
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Tang et al. (2026) studied this question.
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