Polysaccharide isolated from Phellinus linteus mycelia exerts anti-inflammatory effects via MAPK and PPAR signaling pathways

Carbohydr Polym. 2018 Nov 15:200:487-497. doi: 10.1016/j.carbpol.2018.08.021. Epub 2018 Aug 8.

Abstract

In the present study, the anti-inflammatory function of Phellinus linteus polysaccharide (PLP) was investigated in animal and cell inflammation models, and the anti-inflammatory mechanism of PLP was also explored. Sixty 8-week ICR mice were randomly divided into 3 groups, and DSS group and DSS + PLP group mice received 2.0% DSS and PLP was orally administered at 500 mg/kg/day. Our data showed that PLP administration obviously improved the health status of mice and inhibited DSS-induced pathological alterations and significantly reduced inflammatory cytokine expressions in the colonic tissues. In lipopolysaccharide-induced inflammation cell model, PLP supplement also significantly reduced inflammatory cytokine expressions and inhibited MAPK pathway as well as the translocations of NF-κB and AP-1. Meanwhile, PLP supplement regulated PPARα and PPARγ phosphorylation and blocked MAPK activation. Taken together, PLP exhibits anti-inflammatory function and its molecular mechanism may be involved in MAPK and PPAR signal pathways, which reduce the expressions of inflammatory cytokines.

Keywords: AP-1; Colitis; Inflammation; MAPK; NF-κB; PPAR; Phellinus linteuspolysaccharide (PLP).

MeSH terms

  • Animals
  • Anti-Inflammatory Agents / chemistry
  • Anti-Inflammatory Agents / isolation & purification
  • Anti-Inflammatory Agents / pharmacology*
  • Basidiomycota / chemistry*
  • Cell Proliferation / drug effects
  • Colon / drug effects
  • Colon / metabolism
  • Cytokines / metabolism
  • Fungal Polysaccharides / chemistry
  • Fungal Polysaccharides / isolation & purification
  • Fungal Polysaccharides / pharmacology*
  • Gene Expression Regulation / drug effects
  • Hep G2 Cells
  • Humans
  • MAP Kinase Signaling System / drug effects*
  • Macrophages / drug effects
  • Macrophages / metabolism
  • Male
  • Malondialdehyde / metabolism
  • Mice
  • NF-kappa B / metabolism
  • Nitrites / metabolism
  • Peroxidase / metabolism
  • Peroxisome Proliferator-Activated Receptors / metabolism*
  • Phosphorylation / drug effects
  • RAW 264.7 Cells
  • Spleen / drug effects
  • Spleen / metabolism
  • Transcription Factor AP-1 / metabolism

Substances

  • Anti-Inflammatory Agents
  • Cytokines
  • Fungal Polysaccharides
  • NF-kappa B
  • Nitrites
  • Peroxisome Proliferator-Activated Receptors
  • Transcription Factor AP-1
  • Malondialdehyde
  • Peroxidase