Quercetin and kaempferol suppress immunoglobulin E-mediated allergic inflammation in RBL-2H3 and Caco-2 cells

Inflamm Res. 2010 Oct;59(10):847-54. doi: 10.1007/s00011-010-0196-2. Epub 2010 Apr 13.

Abstract

Objective: We investigated the inhibitory effects of quercetin and kaempferol treatment on the suppression of immunoglobulin E (IgE)-mediated allergic responses in relation to intestinal epithelium barrier function in RBL-2H3 and Caco-2 cells.

Methods: RBL-2H3 cells as a model of intestinal mucosa mast cells were treated with flavonols followed by IgE-anti-dinitrophenyl sensitization. The extent of degranulation and the release of pro-inflammatory cytokines were measured. Caco-2 cells were stimulated with interleukin (IL)-4 or IgE-allergen with or without flavonol pretreatment and changes in the expression of CD23 mRNA and mitogen-activated protein kinase (MAPK), and chemokine release were determined.

Results: Flavonols inhibited the secretion of allergic mediators in RBL-2H3 cells and suppressed the CD23 mRNA expression and p38 MAPK activation in IL-4 stimulated Caco-2 cells. Flavonols also suppressed IgE-OVA induced extra signal-regulated protein kinase (ERK) activation and chemokine release.

Conclusions: Quercetin and kaempferol effectively suppressed the development of IgE-mediated allergic inflammation of intestinal cell models.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antioxidants / chemistry
  • Antioxidants / pharmacology*
  • Caco-2 Cells* / drug effects
  • Caco-2 Cells* / immunology
  • Chemokine CCL20 / immunology
  • Extracellular Signal-Regulated MAP Kinases / immunology
  • Food Hypersensitivity / immunology
  • Humans
  • Hypersensitivity / immunology*
  • Immunoglobulin E / immunology*
  • Inflammation / immunology*
  • Interleukin-8 / immunology
  • Intestinal Mucosa / cytology
  • Kaempferols / chemistry
  • Kaempferols / immunology
  • Kaempferols / pharmacology*
  • Molecular Structure
  • Quercetin / chemistry
  • Quercetin / immunology
  • Quercetin / pharmacology*
  • Receptors, IgE / genetics
  • Receptors, IgE / immunology
  • p38 Mitogen-Activated Protein Kinases / immunology

Substances

  • Antioxidants
  • Chemokine CCL20
  • Interleukin-8
  • Kaempferols
  • Receptors, IgE
  • Immunoglobulin E
  • kaempferol
  • Quercetin
  • Extracellular Signal-Regulated MAP Kinases
  • p38 Mitogen-Activated Protein Kinases