Luteolin inhibits proliferation and affects the function of stimulated rat synovial fibroblasts

Cell Biol Int. 2009 Feb;33(2):135-47. doi: 10.1016/j.cellbi.2008.10.005. Epub 2008 Oct 22.

Abstract

Hyperproliferation of synovial fibroblasts is considered to be a pivotal event in the pathogenesis of rheumatoid arthritis (RA). Luteolin, a flavonoid, inhibits the proliferation of synovial fibroblasts in collagen-induced arthritic rats. Treatment with luteolin also decreases the secretion of matrix metalloprotease-1 and -3 and the expression of IL-6, IL-8, IL-15, and TGF-beta. Luteolin treatment caused a delay of cells in the G(2)/M phase. Interestingly, combination treatment with luteolin and TNF-alpha exhibited a synergistic inhibitory effect in all experiments. Western blotting demonstrated that treatment with luteolin alone or combined with TNF-alpha inhibited the MAPK/ERKs and PI3K-Akt pathways. These results indicate that luteolin inhibits the proliferation and partially blocks the pathogenic function of synovial fibroblasts in rheumatoid arthritis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Division
  • Cell Proliferation / drug effects*
  • Cytokines / metabolism
  • Drug Synergism
  • Fibroblasts / drug effects*
  • Fibroblasts / metabolism
  • G2 Phase
  • Luteolin / pharmacology*
  • MAP Kinase Signaling System / drug effects
  • Matrix Metalloproteinases / metabolism
  • Phosphatidylinositol 3-Kinases / metabolism
  • Rats
  • Synovial Membrane / cytology*
  • Tumor Necrosis Factor-alpha / pharmacology

Substances

  • Cytokines
  • Tumor Necrosis Factor-alpha
  • Phosphatidylinositol 3-Kinases
  • Matrix Metalloproteinases
  • Luteolin