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March 12, 2026Pharmaceuticals0 citationsOpen Access

Xiebai San Alleviates Allergic Pulmonary Inflammation by Modulating Arachidonic Acid Metabolism

XYXingnan YueJHJiayin HanCPChang Pan

Key Points

  • The central aim was to explore how Xiebai San alleviates allergic pulmonary inflammation and its associated mechanisms.
  • Established two murine models: one chronic (ovalbumin-induced) and one acute (compound 48/80-induced).
  • Evaluated pharmacodynamic indices including serum IgE and histamine levels.
  • Used network pharmacology to predict key pathways involved.
  • Assessed arachidonic acid metabolites using UPLC-MS/MS.
  • Examined p38 MAPK signaling proteins with Western blot analysis.
  • Xiebai San significantly alleviated lung injury in both chronic and acute models.
  • In the chronic model, it reduced serum IgE levels and inflammatory cell infiltration.
  • In the acute model, it suppressed histamine release and mast cell-mediated responses.
  • Targeted metabolomics showed that Xiebai San regulated arachidonic acid metabolites differently in each model.
  • Network pharmacology highlighted AA metabolism as a key pathway.

Abstract

Background: Xiebai San (XBS), a classical Traditional Chinese Medicine formula comprising Cortex mori, Lycii Radicis Cortex, and Glycyrrhizae Radix et Rhizoma, has long been used for pulmonary inflammatory disorders. However, its underlying mechanisms remain un-clear. This study aimed to investigate the mechanisms by which XBS alleviates allergic pulmonary inflammation. Methods: Two murine models were established, consisting of a chronic ovalbumin (OVA)-induced model simulating adaptive immune responses and an acute compound 48/80-induced model triggering non-IgE-dependent mast cell activation. Pharmacodynamic indices including serum IgE, histamine, inflammatory cytokines, leukocyte profiles, and lung histopathology were evaluated. Network pharmacology was employed to predict core pathways. Arachidonic acid metabolites (AAMs) in lung tissues were quantified by targeted UPLC-MS/MS, and p38 MAPK signaling proteins were assessed by Western blot. Results: XBS significantly alleviated lung injury in both models. In the chronic OVA-induced model, XBS significantly reduced serum immunoglobulin E levels and inflammatory cell infiltration. In the acute model, XBS suppressed histamine release and mast cell-mediated inflammatory responses. Targeted metabolomics revealed differential regulatory mechanisms: XBS reduced lipoxygenase-derived metabolites, including leukotrienes and 12-hydroxyeicosatetraenoic acid in chronic inflammation, while suppressing cyclooxygenase-related prostaglandins in acute inflammation. Network pharmacology analysis identified arachidonic acid (AA) metabolism as a potential central pathway. The p38 mitogen-activated protein kinase pathway was partially involved. Conclusions: XBS effectively alleviates both chronic and acute allergic pulmonary inflammation through differential modulation of AA metabolism, providing mechanistic insights supporting its traditional use in allergic airway diseases.

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Cite This Study

Yue et al. (2026) studied this question.

synapsesocial.com/papers/69b2581996eeacc4fcec7685https://doi.org/10.3390/ph19030440
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