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        <identifier>oai:figshare.com:article/34023674</identifier>
        <datestamp>2026-09-29T12:11:28Z</datestamp>
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          <dc:title>Integrative multi-omics analysis of network pharmacology reveals the active components and mechanisms of &lt;i&gt;Olibanun&lt;/i&gt; in improving atopic dermatitis</dc:title>
          <dc:creator>Xiaobi Zhang (25136990)</dc:creator>
          <dc:creator>Pengyuan Du (17507646)</dc:creator>
          <dc:creator>Wenqi Tang (4675531)</dc:creator>
          <dc:creator>Yinling Zhou (25136993)</dc:creator>
          <dc:creator>Jing Cao (287196)</dc:creator>
          <dc:creator>Lusheng Wang (513360)</dc:creator>
          <dc:creator>Jianli Pan (25136996)</dc:creator>
          <dc:subject>Biochemistry</dc:subject>
          <dc:subject>Microbiology</dc:subject>
          <dc:subject>Cell Biology</dc:subject>
          <dc:subject>Molecular Biology</dc:subject>
          <dc:subject>Biotechnology</dc:subject>
          <dc:subject>Immunology</dc:subject>
          <dc:subject>Biological Sciences not elsewhere classified</dc:subject>
          <dc:subject>Developmental Biology</dc:subject>
          <dc:subject>Olibanun</dc:subject>
          <dc:subject>atopic dermatitis</dc:subject>
          <dc:subject>network pharmacology</dc:subject>
          <dc:subject>single-cell sequencing g</dc:subject>
          <dc:subject>immune microenvironment</dc:subject>
          <dc:subject>keratinocyte-T-cell communication axis</dc:subject>
          <dc:description>&lt;p&gt;This study investigates potential active ingredients of Olibanun in ameliorating atopic dermatitis (AD) and underlying mechanisms. 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. DNCB-induced AD mice tested &lt;i&gt;Olibanun&lt;/i&gt; 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. &lt;i&gt;In vitro,&lt;/i&gt; 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.&lt;/p&gt;</dc:description>
          <dc:date>2026-09-29T12:11:28Z</dc:date>
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          <dc:identifier>10.6084/m9.figshare.34023674.v1</dc:identifier>
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          <dc:rights>CC BY 4.0</dc:rights>
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