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Selective N-acylethanolamine-hydrolyzing acid amidase inhibition reveals a key role for endogenous palmitoylethanolamide in inflammation.

Abstract
Identifying points of control in inflammation is essential to discovering safe and effective antiinflammatory medicines. Palmitoylethanolamide (PEA) is a naturally occurring lipid amide that, when administered as a drug, inhibits inflammatory responses by engaging peroxisome proliferator-activated receptor-alpha (PPAR-alpha). PEA is preferentially hydrolyzed by the cysteine amidase N-acylethanolamine-hydrolyzing acid amidase (NAAA), which is highly expressed in macrophages. Here we report the discovery of a potent and selective NAAA inhibitor, N-[(3S)-2-oxo-3-oxetanyl]-3-phenylpropanamide [(S)-OOPP], and show that this inhibitor increases PEA levels in activated leukocytes and blunts responses induced by inflammatory stimuli both in vitro and in vivo. These effects are stereoselective, mimicked by exogenous PEA, and abolished by PPAR-alpha deletion. (S)-OOPP also attenuates inflammation and tissue damage and improves recovery of motor function in mice subjected to spinal cord trauma. The results suggest that PEA activation of PPAR-alpha in leukocytes serves as an early stop signal that contrasts the progress of inflammation. The PEA-hydrolyzing amidase NAAA may provide a previously undescribed target for antiinflammatory medicines.
AuthorsCarlos Solorzano, Chenggang Zhu, Natalia Battista, Giuseppe Astarita, Alessio Lodola, Silvia Rivara, Marco Mor, Roberto Russo, Mauro Maccarrone, Francesca Antonietti, Andrea Duranti, Andrea Tontini, Salvatore Cuzzocrea, Giorgio Tarzia, Daniele Piomelli
JournalProceedings of the National Academy of Sciences of the United States of America (Proc Natl Acad Sci U S A) Vol. 106 Issue 49 Pg. 20966-71 (Dec 08 2009) ISSN: 1091-6490 [Electronic] United States
PMID19926854 (Publication Type: Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't)
Chemical References
  • Amides
  • Anti-Inflammatory Agents
  • Butyrates
  • Endocannabinoids
  • Enzyme Inhibitors
  • Ethanolamines
  • GW 7647
  • PPAR alpha
  • Palmitic Acids
  • Phenylpropionates
  • Phenylurea Compounds
  • palmidrol
  • Carrageenan
  • Amidohydrolases
  • fatty-acid amide hydrolase
Topics
  • Amides
  • Amidohydrolases (antagonists & inhibitors, metabolism)
  • Animals
  • Anti-Inflammatory Agents (pharmacology)
  • Butyrates (pharmacology)
  • Carrageenan
  • Catalytic Domain
  • Cell Movement (drug effects)
  • Drug Discovery
  • Endocannabinoids
  • Enzyme Inhibitors (pharmacology)
  • Ethanolamines
  • Inflammation (enzymology, pathology)
  • Mice
  • Mice, Inbred C57BL
  • Neutrophils (cytology, drug effects, enzymology)
  • PPAR alpha (agonists)
  • Palmitic Acids (metabolism)
  • Phenylpropionates (pharmacology)
  • Phenylurea Compounds (pharmacology)
  • Spinal Cord Injuries (enzymology, pathology)

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