Impaired decision making following escalation of cocaine self-administration predicts vulnerability to relapse in rats

Addict Biol. 2020 May;25(3):e12738. doi: 10.1111/adb.12738. Epub 2019 Mar 7.

Abstract

Impairments in cost-benefit decision making represent a cardinal feature of drug addiction. However, whether these alterations predate drug exposure, thereby contributing to facilitating loss of control over drug intake, or alternatively arise as a result of drug use and subsequently confer vulnerability to relapse has yet to be determined. Male Sprague-Dawley rats were trained to self-administer (SA) cocaine during 19 daily long-access (12-h) sessions; conditions reliably shown to promote escalation. One week after cocaine SA, rats underwent an extinction/relapse test immediately followed by conditioned stimuli-, stress-, and drug-primed reinstatement challenges. The influence of escalated cocaine intake on decision making was measured over time by four test sessions of a rodent analogue of the Iowa Gambling Task (rGT), once prior to cocaine exposure and then 1 day, 1 week, and 1 month after the last SA session. Substantial individual variability was observed in the influence of escalated cocaine SA on decision-making performance. A subset of rats displayed pronounced deficits, while others showed unaffected or even improved performance on the rat Gambling Task (rGT) 24 hours after the last SA session. When challenged with a relapse test after 1 week of forced abstinence, animals that showed impaired decision making following SA displayed an increased propensity to respond for cocaine under extinction. These data suggest that decision-making deficits in individuals with drug addiction are not antecedent to-but arise as a consequence of-drug exposure. Moreover, these data indicate that susceptibility to the deleterious effects of drugs on decision making confers vulnerability toward relapse.

Keywords: Iowa Gambling Task; addiction; cocaine; decision making; escalation; relapse.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Behavior, Animal
  • Cocaine / administration & dosage*
  • Cocaine-Related Disorders / psychology*
  • Decision Making*
  • Disease Models, Animal
  • Dopamine Uptake Inhibitors / administration & dosage*
  • Extinction, Psychological
  • Male
  • Rats
  • Rats, Sprague-Dawley
  • Recurrence
  • Self Administration

Substances

  • Dopamine Uptake Inhibitors
  • Cocaine