The ameliorative effect of sophoricoside on mast cell-mediated allergic inflammation in vivo and in vitro

Molecules. 2013 May 22;18(5):6113-27. doi: 10.3390/molecules18056113.

Abstract

Sophoricoside exhibits numerous pharmacological effects, including anti- inflammatory and anti-cancer actions, yet the exact mechanism that accounts for the anti-allergic effects of sophoricoside is not completely understood. The aim of the present study was to elucidate whether and how sophoricoside modulates the mast cell-mediated allergic inflammation in vitro and in vivo. We investigated the pharmacological effects of sophoricoside on both compound 48/80 or histamine-induced scratching behaviors and 2,4-dinitrochlorobenzene (DNCB)-induced atopic dermatitis in mice. Additionally, to find a possible explanation for the anti-inflammatory effects of sophoricoside, we evaluated the effects of sophoricoside on the production of histamine and inflammatory cytokines and activation of nuclear factor-κB (NF-κB) and caspase-1 in phorbol 12-myristate 13-acetate plus calcium ionophore A23187 (PMACI)-stimulated human mast cells (HMC-1). The finding of this study demonstrated that sophoricoside reduced compound 48/80 or histamine-induced scratching behaviors and DNCB-induced atopic dermatitis in mice. Additionally, sophoricoside inhibited the production of inflammatory cytokines as well as the activation of NF-κB and caspase-1 in stimulated HMC-1. Collectively, the findings of this study provide us with novel insights into the pharmacological actions of sophoricoside as a potential molecule for use in the treatment of allergic inflammation diseases.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Anti-Inflammatory Agents / pharmacology*
  • Benzopyrans / pharmacology*
  • Calcimycin / pharmacology
  • Calcium Ionophores / pharmacology
  • Carcinogens / pharmacology
  • Caspase 1 / metabolism
  • Cell Line
  • Cytokines / metabolism
  • Dermatitis, Atopic / chemically induced
  • Dermatitis, Atopic / drug therapy*
  • Dermatitis, Atopic / metabolism
  • Dermatitis, Atopic / pathology
  • Dinitrochlorobenzene / adverse effects
  • Dinitrochlorobenzene / pharmacology
  • Histamine / metabolism
  • Humans
  • Irritants / adverse effects
  • Irritants / pharmacology
  • Male
  • Mast Cells / metabolism*
  • Mast Cells / pathology
  • Mice
  • Mice, Inbred BALB C
  • Mice, Inbred ICR
  • NF-kappa B / metabolism
  • Tetradecanoylphorbol Acetate / pharmacology

Substances

  • Anti-Inflammatory Agents
  • Benzopyrans
  • Calcium Ionophores
  • Carcinogens
  • Cytokines
  • Dinitrochlorobenzene
  • Irritants
  • NF-kappa B
  • sophoricoside
  • Calcimycin
  • Histamine
  • Caspase 1
  • Tetradecanoylphorbol Acetate