Inhibition of N-acylethanolamine acid amidase reduces nicotine-induced dopamine activation and reward

Neuropharmacology. 2019 Jan;144:327-336. doi: 10.1016/j.neuropharm.2018.11.013. Epub 2018 Nov 12.

Abstract

Tobacco smoke is the leading preventable cause of death in the world and treatments aimed to increase success rate in smoking cessation by reducing nicotine dependence are sought. Activation of peroxisome proliferator-activated receptor-alpha (PPARα) by synthetic or endogenous agonists was shown to suppress nicotine-induced activation of mesolimbic dopamine system, one of the major neurobiological substrates of nicotine dependence, and nicotine-seeking behavior in rats and monkeys. An alternative indirect way to activate PPARα is inhibition of N-acylethanolamine acid amidase (NAAA), one of the major hydrolyzing enzyme for its endogenous agonists palmitoylethanolamide (PEA) and oleoylethanolamide (OEA). We synthetized a novel specific brain permeable NAAA inhibitor, AM11095. We administered AM11095 to rats and carried out brain lipid analysis, a functional observational battery (FOB) to assess toxicity, in vivo electrophysiological recording from dopamine cells in the ventral tegmental area, brain microdialysis in the nucleus accumbens shell and behavioral experiments to assess its effect on nicotine -induced conditioned place preference (CPP). AM11095 (5 and 25 mg/kg, i.p.) was devoid of neurotoxic and behavioral effects and did not affect motor behavior and coordination. This NAAA inhibitor (5 mg/kg i.p.) increased OEA and PEA levels in the hippocampus and cortex, prevented nicotine-induced activation of mesolimbic dopamine neurons in the ventral tegmental area, nicotine-induced elevation of dopamine levels in the nucleus accumbens shell and decreased the expression of nicotine CPP. Our results indicate that NAAA inhibitors represent a new class of pharmacological tools to modulate brain PEA/PPARα signalling and show potential in the treatment of nicotine dependence.

Keywords: Conditioned place preference; Dopamine; Electrophysiology; Microdialysis; NAAA inhibitor; Nicotine; PPARα.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amidohydrolases / antagonists & inhibitors*
  • Amidohydrolases / metabolism
  • Animals
  • Brain / drug effects
  • Brain / metabolism
  • Conditioning, Psychological / drug effects
  • Conditioning, Psychological / physiology
  • Dopamine / metabolism*
  • Drug Evaluation, Preclinical
  • Enzyme Inhibitors / pharmacokinetics
  • Enzyme Inhibitors / pharmacology
  • Enzyme Inhibitors / toxicity
  • Male
  • Mice
  • Nicotine / pharmacology*
  • Nicotinic Agonists / pharmacology
  • Psychotropic Drugs / pharmacology*
  • Random Allocation
  • Rats, Sprague-Dawley
  • Reward*
  • Spatial Behavior / drug effects
  • Spatial Behavior / physiology

Substances

  • Enzyme Inhibitors
  • Nicotinic Agonists
  • Psychotropic Drugs
  • Nicotine
  • Amidohydrolases
  • N-acylethanolamine-hydrolyzing acid amidase, rat
  • Dopamine