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March 29, 2026Antioxidants0 citationsOpen Access

Ameliorating Effects of Phlomis umbrosa Turcz. Root in Ovalbumin-Induced Allergic Asthma: Modulation of IL-33-Mediated Inflammation and TGF-β/Smad-Dependent Fibrosis

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YJYuefeng JuHLHyo Lim LeeHCHye Ji Choi

Key Points

  • The study aims to evaluate the therapeutic effects of Phlomis umbrosa root extract on allergic asthma.
  • Utilized a mouse model induced with ovalbumin to simulate allergic asthma.
  • Conducted phytochemical analysis to identify bioactive compounds in the extract.
  • Quantitatively analyzed shanzhiside methyl ester as a primary active ingredient.
  • Evaluated immune response and physiological changes post-treatment.
  • EPT reduced the Th2 immune response associated with asthma.
  • Significantly decreased eosinophilia and related histopathological changes.
  • Inhibited the activation of IL-33 and TGF-β signaling pathways.
  • Reduced inflammation and fibrosis while promoting decreased apoptosis.

Abstract

Our study aimed to evaluate the therapeutic potential of a 20% ethanolic extract of the Phlomis umbrosa Turcz. (EPT) herb and its associated bioactive compounds in an ovalbumin (OVA)-induced allergic asthma mouse model. We used phytochemical analysis and identified sesamoside, shanzhiside methyl ester, 8-O-acetyl shanzhiside methyl ester, and isoacteoside as the bioactive components. We validated and quantitatively analyzed shanzhiside methyl ester as a major compound. The treatment with EPT significantly attenuated the T helper type 2 (Th2)-based immune response, eosinophilia, histopathological changes, and biochemical parameters. Furthermore, EPT inhibited interleukin (IL)-33-mediated activation of the nuclear factor kappa B (NF-κB) and transforming growth factor beta (TGF-β) signaling pathways, as well as reduced fibrosis and apoptosis associated with inflammation. The findings of our study suggest that EPT is a promising natural substance for alleviating symptoms of allergic asthma.

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Cite This Study

Ju et al. (2026) studied this question.

synapsesocial.com/papers/69c8c30dde0f0f753b39da86https://doi.org/10.3390/antiox15040420
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