JNJ-39220675, a novel selective histamine H3 receptor antagonist, reduces the abuse-related effects of alcohol in rats

Psychopharmacology (Berl). 2011 Apr;214(4):829-41. doi: 10.1007/s00213-010-2092-4. Epub 2010 Nov 18.

Abstract

Rationale: A few recent studies suggest that brain histamine levels and signaling via H(3) receptors play an important role in modulation of alcohol stimulation and reward in rodents.

Objective: The present study characterized the effects of a novel, selective, and brain penetrant H(3) receptor antagonist (JNJ-39220675) on the reinforcing effects of alcohol in rats.

Methods: The effect of JNJ-39220675 on alcohol intake and alcohol relapse-like behavior was evaluated in selectively bred alcohol-preferring (P) rats using the standard two-bottle choice method. The compound was also tested on operant alcohol self administration in non-dependent rats and on alcohol-induced ataxia using the rotarod apparatus. In addition, alcohol-induced dopamine release in the nucleus accumbens was tested in freely moving rats.

Results: Subcutaneous administration of the selective H(3) receptor antagonist dose-dependently reduced both alcohol intake and preference in alcohol-preferring rats. JNJ-39220675 also reduced alcohol preference in the same strain of rats following a 3-day alcohol deprivation. The compound significantly and dose-dependently reduced alcohol self-administration without changing saccharin self-administration in alcohol non-dependent rats. Furthermore, the compound did not change the ataxic effects of alcohol, alcohol elimination rate, nor alcohol-induced dopamine release in nucleus accumbens.

Conclusions: These results indicate that blockade of H(3) receptor should be considered as a new attractive mechanism for the treatment of alcoholism.

MeSH terms

  • Alcoholism / drug therapy*
  • Alcoholism / metabolism
  • Alcoholism / psychology
  • Animals
  • Autoradiography
  • Azepines / pharmacology
  • Azepines / therapeutic use*
  • Behavior, Animal / drug effects
  • Brain / metabolism
  • Histamine H3 Antagonists / pharmacokinetics
  • Histamine H3 Antagonists / pharmacology
  • Histamine H3 Antagonists / therapeutic use*
  • Injections, Subcutaneous
  • Male
  • Microdialysis
  • Molecular Structure
  • Motor Activity / drug effects
  • Protein Binding
  • Pyridines / pharmacology
  • Pyridines / therapeutic use*
  • Rats
  • Rats, Sprague-Dawley
  • Receptors, Histamine H3 / metabolism
  • Reinforcement, Psychology
  • Self Administration

Substances

  • (4-cyclobutyl-(1,4)diazepan-1-yl)-(6-(4-fluorophenoxy)pyridin-3-yl)methanone
  • Azepines
  • Histamine H3 Antagonists
  • Pyridines
  • Receptors, Histamine H3