Amitifadine, a triple monoamine uptake inhibitor, reduces binge drinking and negative affect in an animal model of co-occurring alcoholism and depression symptomatology

Pharmacol Biochem Behav. 2012 Nov;103(1):111-8. doi: 10.1016/j.pbb.2012.07.014.

Abstract

The co-occurrence of alcoholism and depression is highly prevalent and difficult to treat. In an animal model of binge drinking that exhibits abstinence-induced behaviors reminiscent of negative affective states, the triple monoamine uptake inhibitor, amitifadine, produced a selective, dose dependent attenuation of binge drinking. Amitifadine also reversed abstinence-induced increases in the intracranial self-stimulation threshold, a model of anhedonia, and immobility in the forced swim test, reflecting behavioral despair. In view of the safety profile of amitifadine in humans, including low risk for weight gain, lack of sexual side effects, and low potential for abuse, we hypothesize that amitifadine will be effective in treating co-occurring alcoholism and depression.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Affect / drug effects*
  • Alcoholism / complications
  • Alcoholism / drug therapy
  • Alcoholism / physiopathology
  • Alcoholism / psychology
  • Animals
  • Aza Compounds / pharmacology*
  • Binge Drinking / drug therapy*
  • Binge Drinking / physiopathology
  • Binge Drinking / psychology
  • Biogenic Monoamines / metabolism
  • Bridged Bicyclo Compounds, Heterocyclic / pharmacology*
  • Depression / complications
  • Depression / drug therapy
  • Depression / physiopathology
  • Depression / psychology
  • Disease Models, Animal
  • Ethanol / blood
  • Humans
  • Imipramine / pharmacology
  • Male
  • Motor Activity / drug effects
  • Rats

Substances

  • 1-(3,4-dichlorophenyl)-3-azabicyclo-(3.1.0)hexane hydrochloride
  • Aza Compounds
  • Biogenic Monoamines
  • Bridged Bicyclo Compounds, Heterocyclic
  • Ethanol
  • Imipramine