Central administration of palmitoylethanolamide reduces hyperalgesia in mice via inhibition of NF-kappaB nuclear signalling in dorsal root ganglia

Eur J Pharmacol. 2009 Jun 24;613(1-3):54-9. doi: 10.1016/j.ejphar.2009.04.022. Epub 2009 Apr 20.

Abstract

Despite the clear roles played by peroxisome proliferators-activated receptor alpha (PPAR-alpha) in lipid metabolism, inflammation and feeding, the effects of its activation in the central nervous system (CNS) are largely unknown. Palmitoylethanolamide (PEA), a member of the fatty-acid ethanolamide family, acts peripherally as an endogenous PPAR-alpha agonist, exerting analgesic and anti-inflammatory effects. Both PPAR-alpha and PEA are present in the CNS, but the specific functions of this lipid and its receptor remain to be clarified. Using the carrageenan-induced paw model of hyperalgesia in mice, we report here that intracerebroventricular administration of PEA (0.1-1 microg) 30 min before carrageenan injection markedly reduced mechanical hyperalgesia up to 24 h following inflammatory insult. This effect was mimicked by GW7647 (1 microg), a synthetic PPAR-alpha agonist. The obligatory role of PPAR-alpha in mediating PEA's actions was confirmed by the lack of anti-hyperalgesic effects in mutant mice lacking PPAR-alpha. PEA significantly reduced the expression of cyclooxygenase-2 (COX-2) and inducible nitric oxide synthase (iNOS) in sciatic nerves and restored carrageenan-induced reductions of PPAR-alpha in the L4-L6 dorsal root ganglia (DRG). To investigate the mechanism by which PEA attenuated hyperalgesia, we evaluated inhibitory kB-alpha (IkB-alpha) degradation and p65 nuclear factor kB (NF-kappaB) activation in DRG. PEA prevented IkB-alpha degradation and p65 NF-kappaB nuclear translocation, confirming the involvement of this transcriptional factor in the control of peripheral hyperalgesia. These results add further support to the broad-spectrum of biological and pharmacological effects induced by PPAR-alpha agonists, suggesting a centrally mediated component for these drugs in controlling inflammatory pain.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amides
  • Analgesics / administration & dosage
  • Analgesics / pharmacology
  • Analgesics / therapeutic use
  • Animals
  • Butyrates / administration & dosage
  • Butyrates / pharmacology
  • Carrageenan / toxicity
  • Cell Nucleus / drug effects*
  • Cell Nucleus / metabolism
  • Central Nervous System / metabolism
  • Cyclooxygenase 2 / biosynthesis
  • Endocannabinoids
  • Enzyme Induction / drug effects
  • Ethanolamines
  • Ganglia, Spinal / drug effects
  • Ganglia, Spinal / metabolism*
  • Ganglia, Spinal / pathology
  • Hyperalgesia / chemically induced
  • Hyperalgesia / drug therapy
  • Hyperalgesia / metabolism
  • Hyperalgesia / pathology*
  • Male
  • Mice
  • NF-kappa B / metabolism*
  • Nitric Oxide Synthase Type II / biosynthesis
  • PPAR alpha / agonists
  • PPAR alpha / metabolism
  • Palmitic Acids / administration & dosage*
  • Palmitic Acids / pharmacology*
  • Palmitic Acids / therapeutic use
  • Phenylurea Compounds / administration & dosage
  • Phenylurea Compounds / pharmacology
  • Sciatic Nerve / drug effects
  • Sciatic Nerve / metabolism
  • Signal Transduction / drug effects*

Substances

  • Amides
  • Analgesics
  • Butyrates
  • Endocannabinoids
  • Ethanolamines
  • GW 7647
  • NF-kappa B
  • PPAR alpha
  • Palmitic Acids
  • Phenylurea Compounds
  • palmidrol
  • Carrageenan
  • Nitric Oxide Synthase Type II
  • Ptgs2 protein, mouse
  • Cyclooxygenase 2