Palmitoylethanolamide attenuates cocaine-induced behavioral sensitization and conditioned place preference in mice

Pharmacol Biochem Behav. 2018 Mar:166:1-12. doi: 10.1016/j.pbb.2018.01.002. Epub 2018 Jan 11.

Abstract

Cocaine addiction is a chronically relapsing disorder characterized by compulsive drug-seeking and drug-taking behaviors. Previous studies have demonstrated that cocaine, as well as other drugs of abuse, alters the levels of lipid-based signaling molecules, such as N-acylethanolamines (NAEs). Moreover, brain levels of NAEs have shown sensitivity to cocaine self-administration and extinction training in rodents. Given this background, the aim of this study was to investigate the effects of repeated or acute administration of palmitoylethanolamide (PEA), an endogenous NAE, on psychomotor sensitization and cocaine-induced contextual conditioning. To this end, the potential ability of repeated PEA administration (1 or 10 mg/kg, i.p.) to modulate the acquisition of cocaine-induced behavioral sensitization (BS) and conditioned place preference (CPP) was assessed in male C57BL/6J mice. In addition, the expression of cocaine-induced BS and CPP following acute PEA administration were also studied. Results showed that repeated administration of both doses of PEA were able to block the acquisition of cocaine-induced BS. Furthermore, acute administration of both doses of PEA was able to abolish the expression of BS, while the highest dose also abolished the expression of cocaine-induced CPP. Taken together, these results indicate that exogenous administration of PEA attenuated psychomotor sensitization, while the effect of PEA in cocaine-induced CPP depended on whether PEA was administered repeatedly or acutely. These findings could be relevant to understand the role that NAEs play in processes underlying the development and maintenance of cocaine addiction.

Keywords: Cocaine; Conditioned locomotion; Conditioned place preference; Locomotor sensitization; Palmitoylethanolamide.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Akathisia, Drug-Induced / prevention & control*
  • Akathisia, Drug-Induced / psychology
  • Amides
  • Analgesics / administration & dosage*
  • Animals
  • Cocaine / administration & dosage*
  • Cocaine / toxicity
  • Conditioning, Psychological / drug effects*
  • Conditioning, Psychological / physiology
  • Dopamine Uptake Inhibitors / administration & dosage
  • Dopamine Uptake Inhibitors / toxicity
  • Dose-Response Relationship, Drug
  • Ethanolamines / administration & dosage*
  • Injections, Intraperitoneal
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Palmitic Acids / administration & dosage*
  • Psychomotor Performance / drug effects*
  • Psychomotor Performance / physiology

Substances

  • Amides
  • Analgesics
  • Dopamine Uptake Inhibitors
  • Ethanolamines
  • Palmitic Acids
  • palmidrol
  • Cocaine