Curcumin suppresses lipopolysaccharide-induced cyclooxygenase-2 expression by inhibiting activator protein 1 and nuclear factor kappab bindings in BV2 microglial cells

J Pharmacol Sci. 2004 Mar;94(3):325-8. doi: 10.1254/jphs.94.325.

Abstract

Inflammation is a significant component of chronic neurodegenerative diseases. Cyclooxygenase-2 (COX-2) is expressed in activated microglial cells and appears to be an important source of prostaglandins during inflammatory conditions. To investigate the effect of curcumin on COX-2 gene expression in microglial cells, we treated lipopolysaccharide (LPS)-challenged BV2 microglial cells with various concentrations of curcumin. Curcumin significantly inhibited LPS-mediated induction of COX-2 expression in both mRNA and protein levels in a concentration-dependent manner. COX-2 enzyme activity was also inhibited in accordance with mRNA and protein levels. Furthermore, curcumin markedly inhibited LPS-induced nuclear factor kappaB (NF-kappaB) and activator protein 1 (AP-1) DNA bindings. These data suggest that curcumin suppresses LPS-induced COX-2 gene expression by inhibiting NF-kappaB and AP-1 DNA bindings in BV2 microglial cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cells, Cultured*
  • Curcumin / chemistry
  • Curcumin / pharmacology*
  • Cyclooxygenase 2
  • Gene Expression / drug effects
  • Gene Expression / genetics
  • Lipopolysaccharides / antagonists & inhibitors*
  • Lipopolysaccharides / metabolism
  • Lipopolysaccharides / pharmacology
  • Mice
  • Microglia / cytology*
  • Microglia / drug effects
  • Microglia / physiology
  • NF-kappa B / antagonists & inhibitors*
  • NF-kappa B / drug effects
  • NF-kappa B / metabolism
  • Prostaglandin-Endoperoxide Synthases / genetics*
  • Prostaglandin-Endoperoxide Synthases / metabolism
  • Prostaglandins / metabolism
  • RNA, Messenger / drug effects
  • RNA, Messenger / metabolism
  • Transcription Factor AP-1 / antagonists & inhibitors*
  • Transcription Factor AP-1 / drug effects
  • Transcription Factor AP-1 / metabolism

Substances

  • Lipopolysaccharides
  • NF-kappa B
  • Prostaglandins
  • RNA, Messenger
  • Transcription Factor AP-1
  • Cyclooxygenase 2
  • Prostaglandin-Endoperoxide Synthases
  • Curcumin