Involvement of Nrf2-mediated heme oxygenase-1 expression in anti-inflammatory action of chitosan oligosaccharides through MAPK activation in murine macrophages

Eur J Pharmacol. 2016 Dec 15:793:43-48. doi: 10.1016/j.ejphar.2016.11.002. Epub 2016 Nov 6.

Abstract

Chitosan and its derivatives have been reported to have anti-inflammatory effects in vitro and in vivo. It is also suggested that chitosan and its derivatives could be up-regulating heme oxygenase-1 (HO-1) in different models. However, the up-regulation of HO-1 by chitosan oligosaccharides (COS) remains unexplored in regard to anti-inflammatory action in lipopolysaccharide (LPS)-stimulated murine macrophages (RAW264.7 cells). Treatment with COS induced HO-1 expression in LPS-stimulated RAW264.7 cells, whereas the expression of inducible nitric oxide synthase (iNOS) and cyclooxygenase-2 (COX-2) was decreased. Pretreatment with ZnPP, a HO-1 inhibitor, reduced the COS-mediated anti-inflammatory action. HO-1 induction is mediated by activating the nuclear translocation of NF-E2-related factor 2 (Nrf2) using COS. Moreover, COS increased the phosphorylation of extracellular signal regulated kinase (ERK1/2), c-Jun N-terminal kinase/stress-activated protein kinase (JNK), and p38 MAPK. However, specific inhibitors of ERK, JNK, and p38 reduced COS-mediated nuclear translocation of Nrf2. Therefore, HO-1 induction also decreased in RAW264.7 cells. Collectively, COS exert an anti-inflammatory effect through Nrf2/MAPK-mediated HO-1 induction.

Keywords: Anti-inflammatory; Chitosan oligosaccharides; HO-1; MAPKs; Nrf2.

MeSH terms

  • Animals
  • Anti-Inflammatory Agents / chemistry
  • Anti-Inflammatory Agents / pharmacology
  • Chitosan / chemistry
  • Chitosan / pharmacology*
  • Cyclooxygenase 2 / metabolism
  • Cytokines / metabolism
  • Enzyme Activation / drug effects
  • Gene Expression Regulation, Enzymologic / drug effects*
  • Heme Oxygenase-1 / metabolism*
  • MAP Kinase Signaling System / drug effects
  • Macrophages / cytology
  • Macrophages / drug effects*
  • Macrophages / metabolism*
  • Mice
  • Mitogen-Activated Protein Kinases / metabolism*
  • NF-E2-Related Factor 2 / metabolism*
  • Nitric Oxide / metabolism
  • Nitric Oxide Synthase Type II / metabolism
  • RAW 264.7 Cells

Substances

  • Anti-Inflammatory Agents
  • Cytokines
  • NF-E2-Related Factor 2
  • Nitric Oxide
  • Chitosan
  • Nitric Oxide Synthase Type II
  • Heme Oxygenase-1
  • Ptgs2 protein, mouse
  • Cyclooxygenase 2
  • Mitogen-Activated Protein Kinases