Chlorogenic acid inhibits lipopolysaccharide-induced cyclooxygenase-2 expression in RAW264.7 cells through suppressing NF-kappaB and JNK/AP-1 activation

Int Immunopharmacol. 2009 Aug;9(9):1042-8. doi: 10.1016/j.intimp.2009.04.011. Epub 2009 Apr 23.

Abstract

Chlorogenic acid (CGA) is a naturally occurring phenolic acid in human diet. Data obtained from in vivo and in vitro experiments demonstrate that CGA mostly presents anti-oxidant and anti-carcinogenic activities. Here we show that CGA also inhibits lipopolysaccharide (LPS)-induced inflammatory response[AU1] in RAW 264.7 cells. Our results indicated that CGA significantly decreased LPS-induced up-regulation of cyclooxygenase (COX-2) at protein and mRNA levels in RAW 264.7 cells and as a result it inhibited prostaglandin E(2) (PGE(2)) release from LPS-treated RAW 264.7 cells. In the further experiments, LPS-induced activation of nuclear factor-kappaB (NF-kappaB) and c-Jun N-terminal kinase (JNK)-c-Jun-activator protein (AP-1) pathway were suppressed significantly by CGA. In addition, CGA did not affect phosphorylation of extracellular signal-regulated kinase 1/2 (ERK1/2) and p38. In conclusion, CGA suppresses LPS-induced COX-2 expression via attenuating the activation of NF-kappaB and JNK/AP-1 signaling pathways suggesting that CGA, the polyphenol compound in our food, could exert anti-inflammatory effects through inhibiting PGE(2) production.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antioxidants / pharmacology
  • Cell Line
  • Chlorogenic Acid / pharmacology*
  • Cyclooxygenase 2 / biosynthesis*
  • Cyclooxygenase 2 / genetics
  • Cyclooxygenase 2 / immunology
  • Dinoprostone / genetics
  • Dinoprostone / immunology
  • Dinoprostone / metabolism
  • Enzyme Activation / drug effects
  • Gene Expression Regulation / drug effects
  • Gene Expression Regulation / immunology
  • Humans
  • Lipopolysaccharides / pharmacology
  • MAP Kinase Kinase 4 / antagonists & inhibitors
  • Macrophages / drug effects
  • Macrophages / immunology
  • Macrophages / metabolism
  • Macrophages / pathology
  • Mice
  • NF-kappa B / antagonists & inhibitors
  • Signal Transduction / drug effects
  • Signal Transduction / immunology
  • Transcription Factor AP-1 / antagonists & inhibitors
  • Transcriptional Activation / drug effects
  • Transcriptional Activation / immunology

Substances

  • Antioxidants
  • Lipopolysaccharides
  • NF-kappa B
  • Transcription Factor AP-1
  • Chlorogenic Acid
  • Cyclooxygenase 2
  • MAP Kinase Kinase 4
  • Dinoprostone