Glycyrrhetinic acid inhibits contact hypersensitivity induced by trichophytin via dectin-1

Exp Dermatol. 2016 Apr;25(4):299-304. doi: 10.1111/exd.12931. Epub 2016 Feb 26.

Abstract

Trichophyton infection is highly prevalent and tends to be recurrent. Therefore, it is important to develop new therapeutic agents. Previously, we established a mouse model of Trichophyton-induced contact hypersensitivity (CHS) and demonstrated that dectin-1 was involved in inflammation induced by trichophytin, the Trichophyton antigen. Here, we used that model to investigate glycyrrhetinic acid (GA) from plants of the genus Glycyrrhiza as a potential anti-inflammatory agent against superficial mycoses. GA suppressed swelling and the expression of inflammatory cytokines, including macrophage inflammatory protein (MIP)-2, interleukin (IL)-6, tumor necrosis factor (TNF)-α and interferon (IFN)-γ mRNA. Anti-MIP-2 antibody suppressed trichophytin-induced inflammation, and antidectin-1 antibody suppressed zymosan-induced MIP-2 production in keratinocyte cells. These results suggest that MIP-2 is produced by dectin-1 activation and is involved in inflammation associated with CHS to trichophytin. GA also suppressed zymosan-induced MIP-2 and interleukin (IL)-8, production in mouse and human macrophages and keratinocytes. Furthermore, GA suppressed the phosphorylation of spleen tyrosine kinase (Syk) and inhibitor of nuclear factor-kappa B (IκBα) and the degradation of IκBα in zymosan-simulated RAW264.7 cells. The results of this study suggest that GA suppresses inflammation induced by trichophytin, partly by the downregulation of Syk phosphorylation.

Keywords: Syk; dectin-1; glycyrrhetinic acid; trichophytin-induced inflammation model.

MeSH terms

  • Animals
  • Anti-Inflammatory Agents / chemistry*
  • Cell Survival
  • Chemokine CXCL2 / metabolism
  • Cytokines / metabolism
  • Dermatitis, Contact / drug therapy*
  • Enzyme-Linked Immunosorbent Assay
  • Glycyrrhetinic Acid / chemistry*
  • Glycyrrhiza
  • Inflammation
  • Interferon-gamma / metabolism
  • Interleukin-6 / metabolism
  • Keratinocytes / metabolism
  • Lectins, C-Type / chemistry*
  • Macrophages / metabolism
  • Male
  • Mice
  • Mycoses / drug therapy
  • NF-KappaB Inhibitor alpha / metabolism
  • Phosphorylation
  • Syk Kinase / metabolism
  • Trichophytin / adverse effects*
  • Trichophyton
  • Tumor Necrosis Factor-alpha / metabolism
  • Zymosan / chemistry

Substances

  • Anti-Inflammatory Agents
  • Chemokine CXCL2
  • Cytokines
  • Interleukin-6
  • Lectins, C-Type
  • Tumor Necrosis Factor-alpha
  • dectin 1
  • NF-KappaB Inhibitor alpha
  • Trichophytin
  • Interferon-gamma
  • Zymosan
  • Syk Kinase
  • Syk protein, mouse
  • Glycyrrhetinic Acid