Anti-Allergic and Anti-Inflammatory Effects of Neferine on RBL-2H3 Cells.

Int J Mol Sci

Graduate Institute of Biomedical and Pharmaceutical Science, Fu Jen Catholic University, New Taipei City 24205, Taiwan.

Published: October 2021

AI Article Synopsis

  • * This study demonstrated that neferine inhibits mast cell degranulation, cytokine expression, and intracellular calcium elevation when mast cells are stimulated, while also reducing activity in the MAPK/NF-κB pathway.
  • * In mouse models, neferine improved dermatitis symptoms, lowered mast cell infiltration, restored skin barrier proteins, and reduced scratching behavior, highlighting its potential as an effective anti-allergic and anti-inflammatory agent.

Article Abstract

Mast cells play a very important role in skin allergy and inflammation, including atopic dermatitis and psoriasis. In the past, it was found that neferine has anti-inflammatory and anti-aging effects on the skin, but its effect on mast cells has not yet been studied in detail. In this study, we used mast cells (RBL-2H3 cells) and mouse models to study the anti-allergic and inflammatory effects of neferine. First, we found that neferine inhibits the degranulation of mast cells and the expression of cytokines. In addition, we observed that when mast cells were stimulated by A23187/phorbol 12-myristate-13-acetate (PMA), the elevation of intracellular calcium was inhibited by neferine. The phosphorylation of the MAPK/NF-κB pathway is also reduced by pretreatment of neferine. The results of in vivo studies show that neferine can improve the appearance of dermatitis and mast cell infiltration caused by dinitrochlorobenzene (DNCB). Moreover, the expressions of barrier proteins in the skin are also restored. Finally, it was found that neferine can reduce the scratching behavior caused by compound 48/80. Taken together, our results indicate that neferine is a very good anti-allergic and anti-inflammatory natural product. Its effect on mast cells contributes to its pharmacological mechanism.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8536162PMC
http://dx.doi.org/10.3390/ijms222010994DOI Listing

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