Inhibition of LPS-induced iNOS, COX-2 and cytokines expression by poncirin through the NF-kappaB inactivation in RAW 264.7 macrophage cells

Biol Pharm Bull. 2007 Dec;30(12):2345-51. doi: 10.1248/bpb.30.2345.

Abstract

We previously reported that poncirin, a flavanone glycoside isolated from the EtOAc extract of the dried immature fruits of Poncirus trifoliata, is an anti-inflammatory compound that inhibits PGE(2) and IL-6 production. The present work was undertaken to investigate the molecular actions of poncirin in RAW 264.7 macrophage cell line. Poncirin reduced lipopolysaccharide (LPS)-induced protein levels of inducible nitric oxide synthase (iNOS) and cyclooxygenase-2 (COX-2) and the mRNA expressions of iNOS, COX-2, tumor necrosis factor-alpha (TNF-alpha) and interleukin-6 (IL-6) in a concentration-dependent manner, as determined by Western blotting and RT-PCR, respectively. Furthermore, poncirin inhibited the LPS-induced DNA binding activity of nuclear factor-kappaB (NF-kappaB). Moreover, this effect was accompanied by a parallel reduction in IkappaB-alpha degradation and phosphorylation that in by nuclear translocations of p50 and p65 NF-kappaB subunits. Taken together, our data indicate that anti-inflammatory properties of poncirin might be the result from the inhibition iNOS, COX-2, TNF-alpha and IL-6 expression via the down-regulation of NF-kappaB binding activity.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Blotting, Western
  • Cell Line
  • Cell Nucleus / drug effects
  • Cell Nucleus / metabolism
  • Cyclooxygenase 2 / biosynthesis*
  • Cytokines / biosynthesis*
  • Dinoprostone / metabolism
  • Electrophoretic Mobility Shift Assay
  • Flavonoids / pharmacology*
  • Humans
  • Interleukin-6 / metabolism
  • Lipopolysaccharides / antagonists & inhibitors*
  • Lipopolysaccharides / pharmacology*
  • Macrophages / drug effects
  • Macrophages / enzymology*
  • NF-kappa B / antagonists & inhibitors*
  • NF-kappa B p50 Subunit / biosynthesis
  • Nitric Oxide Synthase Type II / biosynthesis*
  • Nitrites / metabolism
  • Poncirus / chemistry
  • RNA / biosynthesis
  • RNA / genetics
  • Reverse Transcriptase Polymerase Chain Reaction
  • Transcription Factor RelA / biosynthesis
  • Tumor Necrosis Factor-alpha / metabolism

Substances

  • Cytokines
  • Flavonoids
  • Interleukin-6
  • Lipopolysaccharides
  • NF-kappa B
  • NF-kappa B p50 Subunit
  • Nitrites
  • Transcription Factor RelA
  • Tumor Necrosis Factor-alpha
  • RNA
  • poncirin
  • Nitric Oxide Synthase Type II
  • Cyclooxygenase 2
  • Dinoprostone