Peroxisome proliferator-activated receptor gamma agonist action of 3-methyl-1,2-cyclopentanedione

Biochim Biophys Acta. 2007 Dec;1770(12):1612-9. doi: 10.1016/j.bbagen.2007.08.006. Epub 2007 Aug 25.

Abstract

Peroxisome proliferator-activated receptors (PPARs) are members of the nuclear hormone receptor superfamily that plays a pivotal role in regulating inflammatory gene expression. The purpose of this study was to investigate the effects of coffee extract, 3-methyl-1,2-cyclopentanedione (3-MCP) on PPARs in vitro. Western blotting and luciferase assays using the PPAR response element (PPRE) construct revealed that 3-MCP induced PPARgamma-selective activation in YPEN-1 cells and that treatment with the PPARgamma selective antagonist, GW9662, was associated with a decrease in 3-MCP-induced PPARgamma activity. The 3-MCP also was shown to suppress reactive species generation and pro-inflammatory transcription factor NF-kappaB activity through PPARgamma activation. Theses results indicate that 3-MCP is a novel PPARgamma agonist and suggests that this agent may have a potential to minimize inflammation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Anilides / pharmacology
  • Animals
  • Blotting, Western
  • Cell Line
  • Cyclopentanes / pharmacology*
  • Down-Regulation / drug effects
  • NF-kappa B / metabolism
  • PPAR gamma / agonists*
  • Rats

Substances

  • 2-chloro-5-nitrobenzanilide
  • Anilides
  • Cyclopentanes
  • NF-kappa B
  • PPAR gamma
  • 3-methyl-1,2-cyclopentanedione