Anti-inflammatory effects of low-molecular weight chitosan oligosaccharides in IgE-antigen complex-stimulated RBL-2H3 cells and asthma model mice

Mi Ja Chung, Jae Kweon Park, Yong Il Park

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158 Scopus citations

Abstract

The anti-inflammatory effects of low-molecular weight chitosan oligosaccharides (LM-COS) prepared from high-molecular weight chitosan by enzymatic digestion were investigated against allergic reaction and allergic asthma in vivo and in vitro. Allergic asthma is an inflammatory disease of the airways associated with enhanced degranulation and cytokine generation. The LM-COS (< 1 kDa), consisting of glucosamine (GlcN) n, n = 3-5, were capable of inhibiting both antigen-stimulated degranulation and cytokine generation in rat basophilic leukemia RBL-2H3 cells. The protective effect of LM-COS against ovalbumin (OVA)-induced lung inflammation in asthma model mice was also examined. Oral administration of LM-COS (16 mg/kg body weight/day) resulted in a significant reduction in both mRNA and protein levels of interleukin (IL)-4, IL-5, IL-13, tumor necrosis factor (TNF)-α in the lung tissue and bronchoalveolar lavage fluid (BALF); The protein levels of IL-4, IL-13 and TNF-α in BALF were decreased by 5.8-fold, 3.0-fold and 9.9-fold, respectively, compared to those in the OVA-sensitized/challenged asthma control group. These results suggest that the oral administration of LM-COS is effective in alleviating the allergic inflammation in vivo and thus can be a good source material for the development of a potent therapeutic agent against mast cell-mediated allergic inflammatory responses and airway inflammation in allergic inflammatory diseases, including asthma.

Original languageEnglish
Pages (from-to)453-459
Number of pages7
JournalInternational Immunopharmacology
Volume12
Issue number2
DOIs
StatePublished - Feb 2012

Bibliographical note

Funding Information:
This work was supported by a grant from the Gyeonggi-do GRRC program , the Research Fund, 2011 of The Catholic University of Korea , and partly by the Research Fund of The Gachon University of Medicine and Science , for which the authors are thankful.

Keywords

  • Asthma
  • Chitosan oligosaccharides
  • Cytokines
  • In vivo activity
  • Inflammation

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