HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Mechanisms of oleoylethanolamide-induced changes in feeding behavior and motor activity.

Abstract
Oleoylethanolamide (OEA), a lipid synthesized in the intestine, reduces food intake and stimulates lipolysis through peroxisome proliferator-activated receptor-alpha. OEA also activates transient receptor potential vanilloid type 1 (TRPV1) in vitro. Because the anorexigenic effect of OEA is associated with delayed feeding onset and reduced locomotion, we examined whether intraperitoneal administration of OEA results in nonspecific behavioral effects that contribute to the anorexia in rats. Moreover, we determined whether circulating levels of other gut hormones are modulated by OEA and whether CCK is involved in OEA-induced anorexia. Our results indicate that OEA reduces food intake without causing a conditioned taste aversion or reducing sodium appetite. It also failed to induce a conditioned place aversion. However, OEA induced changes in posture and reduced spontaneous activity in the open field. This likely underlies the reduced heat expenditure and sodium consumption observed after OEA injection, which disappeared within 1 h. The effects of OEA on motor activity were similar to those of the TRPV1 agonist capsaicin and were also observed with the peroxisome proliferator-activated receptor-alpha agonist Wy-14643. Plasma levels of ghrelin, peptide YY, glucagon-like peptide 1, and apolipoprotein A-IV were not changed by OEA. Finally, antagonism of CCK-1 receptors did not affect OEA-induced anorexia. These results suggest that OEA suppresses feeding without causing visceral illness and that neither ghrelin, peptide YY, glucagon-like peptide 1, apolipoprotein A-IV, nor CCK plays a critical role in this effect. Despite that OEA-induced anorexia is unlikely to be due to impaired motor activity, our data raise a cautionary note in how specific behavioral and metabolic effects of OEA should be interpreted.
AuthorsKarine Proulx, Daniela Cota, Tamara R Castañeda, Matthias H Tschöp, David A D'Alessio, Patrick Tso, Stephen C Woods, Randy J Seeley
JournalAmerican journal of physiology. Regulatory, integrative and comparative physiology (Am J Physiol Regul Integr Comp Physiol) Vol. 289 Issue 3 Pg. R729-37 (Sep 2005) ISSN: 0363-6119 [Print] United States
PMID15879057 (Publication Type: Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, P.H.S.)
Chemical References
  • Hormone Antagonists
  • Imidazoles
  • Pyrimidines
  • oleoylimidazolide
  • pirinixic acid
  • Sodium
  • Proglumide
  • lorglumide
  • Capsaicin
Topics
  • Animals
  • Appetite (drug effects)
  • Avoidance Learning (drug effects)
  • Capsaicin (pharmacology)
  • Conditioning, Psychological (drug effects)
  • Energy Metabolism (drug effects)
  • Feeding Behavior (drug effects)
  • Hormone Antagonists (pharmacology)
  • Hot Temperature
  • Housing, Animal
  • Imidazoles (administration & dosage, pharmacology)
  • Injections, Intraperitoneal
  • Male
  • Motor Activity (drug effects)
  • Proglumide (analogs & derivatives, pharmacology)
  • Pyrimidines (pharmacology)
  • Rats
  • Rats, Long-Evans
  • Sodium
  • Space Perception
  • Taste

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: