Alternative therapeutic advantages of catfish bile on atopic dermatitis: protection of T cell-mediated skin disease via antioxidant activities

J Pharm Pharmacol. 2011 Oct;63(10):1327-35. doi: 10.1111/j.2042-7158.2011.01337.x. Epub 2011 Aug 8.

Abstract

Objectives: In the present study, we aimed to examine the anti-atopic properties of bile from the cat fish, Silurus asotus, to determine its possible use as a pharmaceutical product.

Methods: The anti-atopic activities of cat fish bile were examined in a non-cell antioxidant, in-vitro assay (splenocytes and mast cells) and a 2,4-dinitrochlorobenzene (DNCB)-induced atopic dermatitis-like mouse model.

Results: The results of these experiments revealed that Silurus asotus bile (SAB) scavenges radicals and protects proteins from superoxide attacks, suggesting that SAB suppresses the T helper (Th) type 2-skewed immune response. Th1/Th2 mRNA cytokines (interleukin (IL)-2, interferon (IFN)-γ and IL-4) from mouse splenocytes were effectively inhibited, and the release of β-hexosaminidase in RBL-2H3 mast cells was significantly suppressed by SAB. These results were supported by screening the Th1/Th2 cytokine mRNAs (IL-2, IFN-γ and IL-4) from lymph nodes in DNCB-treated mice. More dramatic results were observed in the histological changes at higher SAB concentrations (5%) compared to the therapeutic control, visualized using hematoxylin-eosin (H&E) staining.

Conclusions: The results presented in this study suggest that SAB may provide functional advantages with regard to treating atopic dermatitis because of its antioxidant and immune-suppressive effects.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antioxidants / pharmacology
  • Antioxidants / therapeutic use*
  • Bile*
  • Biological Products / pharmacology
  • Biological Products / therapeutic use*
  • Catfishes*
  • Complementary Therapies
  • Cytokines / antagonists & inhibitors
  • Cytokines / genetics
  • Dermatitis, Atopic / immunology
  • Dermatitis, Atopic / metabolism
  • Dermatitis, Atopic / therapy*
  • Dinitrochlorobenzene
  • Lymph Nodes / drug effects
  • Lymph Nodes / metabolism
  • Mast Cells / drug effects
  • Mast Cells / metabolism
  • Mice
  • Mice, Inbred BALB C
  • Protein Carbonylation / drug effects
  • RNA, Messenger / metabolism
  • Skin / drug effects*
  • Skin / pathology
  • Spleen / cytology
  • Spleen / drug effects
  • Spleen / metabolism
  • Superoxides / metabolism
  • T-Lymphocytes / metabolism*
  • Th1 Cells / drug effects
  • Th1 Cells / metabolism
  • Th2 Cells / drug effects
  • Th2 Cells / metabolism
  • beta-N-Acetylhexosaminidases / antagonists & inhibitors

Substances

  • Antioxidants
  • Biological Products
  • Cytokines
  • Dinitrochlorobenzene
  • RNA, Messenger
  • Superoxides
  • beta-N-Acetylhexosaminidases