Hispidulin Inhibits Mast Cell-Mediated Allergic Inflammation through Down-Regulation of Histamine Release and Inflammatory Cytokines

Molecules. 2019 Jun 5;24(11):2131. doi: 10.3390/molecules24112131.

Abstract

Hispidulin (4',5,7-trihydroxy-6-methoxyflavone) is a natural compound derived from traditional Chinese medicinal herbs, and it is known to have an anti-inflammatory effect. Here, we investigated the effect of hispidulin on the immunoglobulin E (IgE)-mediated allergic responses in rat basophilic leukemia (RBL)-2H3 mast cells. When RBL-2H3 cells were sensitized with anti-dinitrophenyl (anti-DNP) IgE and subsequently stimulated with DNP-human serum albumin (HSA), histamine and β-hexosaminidase were released from the cells by degranulation of activated mast cells. However, pretreatment with hispidulin before the stimulation of DNP-HSA markedly attenuated release of both in anti-DNP IgE-sensitized cells. Furthermore, we investigated whether hispidulin inhibits anti-DNP IgE and DNP-HSA-induced passive cutaneous anaphylaxis (PCA), as an animal model for Type I allergies. Hispidulin markedly decreased the PCA reaction and allergic edema of ears in mice. In addition, activated RBL-2H3 cells induced the expression of inflammatory cytokines (tumor necrosis factor-α and interleukin-4), which are critical for the pathogenesis of allergic disease, through the activation of c-Jun N-terminal kinase (JNK). Inhibition of JNK activation by hispidulin treatment reduced the induction of cytokine expression in the activated mast cells. Our results indicate that hispidulin might be a possible therapeutic candidate for allergic inflammatory diseases through the suppression of degranulation and inflammatory cytokines expression.

Keywords: Hispidulin; allergy; inflammation; mast cells.

MeSH terms

  • Animals
  • Cell Degranulation / drug effects
  • Cytokines / metabolism*
  • Down-Regulation* / drug effects
  • Flavones / chemistry
  • Flavones / pharmacology
  • Flavones / therapeutic use*
  • Histamine Release* / drug effects
  • Hypersensitivity / complications
  • Hypersensitivity / drug therapy*
  • Immunoglobulin E / metabolism
  • Inflammation / complications
  • Inflammation / drug therapy*
  • Inflammation / pathology
  • Inflammation Mediators / metabolism*
  • JNK Mitogen-Activated Protein Kinases / metabolism
  • Male
  • Mast Cells / drug effects
  • Mast Cells / pathology*
  • Mice, Inbred ICR
  • Passive Cutaneous Anaphylaxis / drug effects
  • Phosphorylation / drug effects

Substances

  • Cytokines
  • Flavones
  • Inflammation Mediators
  • Immunoglobulin E
  • JNK Mitogen-Activated Protein Kinases
  • hispidulin