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Neoagarooligosaccharides prevent septic shock by modulating A20-and cyclooxygenase-2-mediated interleukin-10 secretion in a septic-shock mouse model
- Source :
- Biochemical and biophysical research communications. 486(4)
- Publication Year :
- 2017
-
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.
- Subjects :
- 0301 basic medicine
medicine.medical_treatment
030106 microbiology
Cell
Biophysics
Oligosaccharides
Biochemistry
Sepsis
03 medical and health sciences
Mice
Immune system
medicine
Animals
Secretion
Molecular Biology
Tumor Necrosis Factor alpha-Induced Protein 3
biology
Dose-Response Relationship, Drug
Septic shock
Cell Biology
medicine.disease
Shock, Septic
Interleukin-10
Mice, Inbred C57BL
Interleukin 10
Agar
030104 developmental biology
Cytokine
medicine.anatomical_structure
Treatment Outcome
Cyclooxygenase 2
Immunology
biology.protein
Female
Cyclooxygenase
Subjects
Details
- ISSN :
- 10902104
- Volume :
- 486
- Issue :
- 4
- Database :
- OpenAIRE
- Journal :
- Biochemical and biophysical research communications
- Accession number :
- edsair.doi.dedup.....c69d92792628272982328ed9afc8a0db