Dissociation of buprenorphine-induced locomotor sensitization and conditioned place preference in rats

J. K. Rowlett, T. R. Gibson, M. T. Bardo

Research output: Contribution to journalArticlepeer-review

26 Scopus citations

Abstract

The locomotor and rewarding effects of the opioid mixed agonist-antagonist buprenorphine were assessed in a conditioned place preference (CPP) experiment. Separate groups of rats were given one of three doses of buprenorphine (0.3, 1.0, or 3.0 mg/kg) or saline paired with the white compartment of a CPP apparatus. The following day, all rats received saline paired with the black compartment. After six conditioning trials, rats were given free access to all compartments of the CPP apparatus. Horizontal activity data obtained during conditioning revealed increased activity (i.e., behavioral sensitization) for the three doses on trial 6. Vertical activity data revealed significant increases on trial 6 for the 1.0 and 3.0 mg/kg doses only. Signifacant CPP was obtained with the 0.3 mg/kg and 1.0 mg/kg doses of buprenorphine, but not with the 3.0 mg/kg dose. These data indicate that buprenorphine elicits locomotor sensitization after repeated exposures that follows a linear dose-response relationship. In contrast, these data suggest that the rewarding effects of buprenorphine follow an inverted U-shaped dose-response curve.

Original languageEnglish
Pages (from-to)241-245
Number of pages5
JournalPharmacology Biochemistry and Behavior
Volume49
Issue number1
DOIs
StatePublished - Sep 1994

Bibliographical note

Funding Information:
The authors thank Dr. S. Bowling, P. Robinet, J. Valone, M. Bradley, S. Otto, and K. Shanmughan for technical assistance. This research was supported by USPHS Grants DA05312 and DA07746.

Keywords

  • Behavioral sensitization
  • Buprenorphine
  • Conditioned place preference
  • Drug reward
  • Locomotor activity
  • Opioid mixed agonist-antagonist

ASJC Scopus subject areas

  • Biochemistry
  • Toxicology
  • Pharmacology
  • Clinical Biochemistry
  • Biological Psychiatry
  • Behavioral Neuroscience

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