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Table · dataset · 2026

Integrative multi-omics analysis of network pharmacology reveals the active components and mechanisms of <i>Olibanun</i> in improving atopic dermatitis

Listed in ZivaHub and HKU DataHub and figshare and Loughborough Research Repository and UP Research Data Repository — shown once because both records carry DOI 10.6084/m9.figshare.34023674.v1

<p>This study investigates potential active ingredients of Olibanun in ameliorating atopic dermatitis (AD) and underlying mechanisms.

Description

Active components were screened via TCMSP. Anti-AD targets predicted using multiple databases PPI networks were built with STRING/Cytoscape.

GO/KEGG enrichment performed with R. Molecular docking used AutoDock. RNA-seq analyzed effects on HaCaT cells. TNF-α/IFN-γ-induced AD models evaluated anti-inflammatory effects.

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DNCB-induced AD mice tested <i>Olibanun</i> extract (OE) ointment protection. ScRNA-seq analyzed AD skin heterogeneity. Thirteen active components and 38 anti-AD targets were identified, mainly regulate inflammation and immune-related pathways.

Docking confirmed strong binding to IKBKB. <i>In vitro,</i> active components exerts anti-inflammatory effects via NF-κB. OE ointment alleviated skin inflammation and decreased inflammatory cytokines. ScRNA-seq revealed keratinocyte-T cell axis dysregulation and IL-17/NF-κB signalling activation in AD skin. Olibanun may regulate the IL-17/NF-κB pathway in keratinocytes and modulate keratinocyte-T cell communication linked to AD pathology.</p>

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Inferred from text
RNA sequencing 65% · Single-cell RNA sequencing 65%
Provenance · 5 source records, 57 field assertions
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