A paradigm to investigate the regulation of cocaine self-administration in human cocaine users: a randomized trial

Psychopharmacology (Berl). 2006 Apr;185(3):306-14. doi: 10.1007/s00213-006-0323-5. Epub 2006 Mar 7.

Abstract

Rationale: We recently conducted a pilot study supporting the feasibility, safety, and validity of a human laboratory model of ad libitum cocaine administration in which subjects self-selected the timing of infusions. The current study extends this work to include a randomized design with a test-retest component in a larger sample.

Objectives: To investigate the regulation of cocaine intake by humans and its effects on subjective and cardiovascular responses.

Materials and methods: Subjects were 14 non-treatment seeking volunteers (10 M, 4 F) with cocaine abuse/dependence. Subjects self-administered cocaine infusions (0, 8, 16, and 32 mg/70 kg) over a 2-h period under a fixed ratio 1, 5-min time-out schedule on 4 consecutive days. A fifth session was conducted at 16-mg dose to assess the paradigm's test-retest reliability.

Results: Subjects regulated their cocaine intake in a dose-dependent fashion. Self-reports of cocaine-related subjective effects (e.g., "high" and "stimulated") also varied in a dose-dependent way. Test-retest data and the randomized design support the conclusion that such effects are not due to tolerance or other experimental artifacts.

Conclusion: The current study replicates prior work demonstrating the feasibility, safety, and validity of our human laboratory paradigm of cocaine administration in a larger sample using a randomized design. The current study also shows the test-retest reliability of these methods, establishing its utility for comparisons of experimental interventions (e.g., pharmacological treatments). Finally, the current study suggests that factors other than drug-induced euphoria (i.e., "high") contribute to the regulation of cocaine-taking behaviors in humans.

Publication types

  • Randomized Controlled Trial
  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Adult
  • Behavior, Addictive / physiopathology*
  • Blood Pressure / drug effects
  • Cocaine / administration & dosage*
  • Cocaine / adverse effects
  • Cocaine-Related Disorders / physiopathology*
  • Dose-Response Relationship, Drug
  • Double-Blind Method
  • Female
  • Heart Rate / drug effects
  • Humans
  • Injections, Intravenous
  • Male
  • Middle Aged
  • Self Administration

Substances

  • Cocaine