Neoagarooligosaccharides prevent septic shock by modulating A20-and cyclooxygenase-2-mediated interleukin-10 secretion in a septic-shock mouse model

Biochem Biophys Res Commun. 2017 May 13;486(4):998-1004. doi: 10.1016/j.bbrc.2017.03.152. Epub 2017 Mar 28.

Abstract

Analysis of the signaling mechanism triggered by endotoxin-mediated toll-like receptor-4 activation using immune cell systems or rodent models may help identify potential agents for the prevention of Gram-negative bacteria infection. β-agarase cleaves the β-1,4-linkages of agar to produce neoagarooligosaccharides (NAOs), which have various physiological functions. The aim of this study was to investigate the efficacy of NAOs in preventing experimental sepsis caused by the administration of endotoxin or Gram-negative bacteria. Organ damage and neutrophil infiltration in an endotoxemia and septic-shock mouse model were suppressed by NAOs. Pro-inflammatory cytokine level was decreased, but IL-10 level was increased by NAO-treatment. Further induction by NAOs in the presence of endotoxin was associated with a significant induction of A20 and cyclooxygenase (COX)-2 expressions. Our data suggest that NAOs have a beneficial preventive effect in septic shock correlated with the enhancement of IL-10 via the induction of A20 and COX-2.

Keywords: A20; COX-2; IL-10; Neoagarooligosaccharides; Prevention; Sepsis.

MeSH terms

  • Agar / chemistry
  • Animals
  • Cyclooxygenase 2 / immunology*
  • Dose-Response Relationship, Drug
  • Female
  • Interleukin-10 / immunology*
  • Mice
  • Mice, Inbred C57BL
  • Oligosaccharides / administration & dosage*
  • Oligosaccharides / chemistry
  • Shock, Septic / immunology*
  • Shock, Septic / prevention & control*
  • Treatment Outcome
  • Tumor Necrosis Factor alpha-Induced Protein 3 / immunology*

Substances

  • IL10 protein, mouse
  • Oligosaccharides
  • Interleukin-10
  • Agar
  • Ptgs2 protein, mouse
  • Cyclooxygenase 2
  • Tumor Necrosis Factor alpha-Induced Protein 3
  • Tnfaip3 protein, mouse