Reversal of cocaine-conditioned place preference and mesocorticolimbic Zif268 expression by social interaction in rats

Addict Biol. 2011 Apr;16(2):273-84. doi: 10.1111/j.1369-1600.2010.00285.x. Epub 2011 Feb 11.

Abstract

Little is known how social interaction, if offered as an alternative to drug consumption, affects neural circuits involved in drug reinforcement and substance dependence. Conditioned place preference (CPP) for cocaine (15 mg/kg i.p.) or social interaction (15 minutes) as an alternative stimulus was investigated in male Sprague-Dawley rats. Four social interaction episodes with a male adult conspecific completely reversed cocaine CPP and were even able to prevent reacquisition of cocaine CPP. Social interaction also reversed cocaine CPP-induced expression of the immediate-early gene zif268 in the nucleus accumbens shell, the central and basolateral amygdala and the ventral tegmental area. These findings suggest that social interaction, if offered in a context that is clearly distinct from the previously drug-associated ones, may profoundly decrease the incentive salience of drug-associated contextual stimuli. The novel experimental design facilitates the neurobiological investigation of this phenomenon which may be beneficial for human drug users in treatment.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Brain Mapping
  • Cerebral Cortex / physiopathology*
  • Choice Behavior
  • Cocaine-Related Disorders / genetics*
  • Cocaine-Related Disorders / physiopathology
  • Cocaine-Related Disorders / psychology
  • Conditioning, Psychological / physiology*
  • Early Growth Response Protein 1 / genetics*
  • Extinction, Psychological / physiology
  • Limbic System / physiopathology*
  • Male
  • Mesencephalon / physiopathology*
  • Motivation / physiology
  • Nerve Net / physiopathology
  • Rats
  • Rats, Sprague-Dawley
  • Social Behavior*
  • Substance Withdrawal Syndrome / genetics
  • Substance Withdrawal Syndrome / physiopathology
  • Substance Withdrawal Syndrome / psychology

Substances

  • Early Growth Response Protein 1
  • Egr1 protein, rat