Novelty-induced place preference behavior in rats: Effects of opiate and dopaminergic drugs

M. T. Bardo, J. L. Neisewander, R. C. Pierce

Research output: Contribution to journalArticle

96 Scopus citations

Abstract

In Experiment 1, adult male rats were given eight 30-min exposures to one of two distinct environments. Control animals received either four exposures to each environment or were not exposed to either environment. When given free-choice access to both environments simultaneously, animals spent significantly more time in the novel environment relative to the familiar environment. In these same animals, horizontal and vertical activity rates were lower in the novel environment than in the familiar environment. In Experiments 2-5, animals were assessed for novelty preference behavior under the influence of either morphine (0, 0.1, 0.3, 1.0 or 3.0 mg/kg), naltrexone (0, 0.1, 0.3 or 1.0 mg/kg), amphetamine (0, 0.1, 0.3 or 1.0 mg/kg) or haloperidol (0, 0.03, 0.1, 0.3 or 1.0 mg/kg). Haloperidol produced a dose-dependent disruption in novelty preference behavior, while all other drugs tested were without effect. Haloperidol also disrupted the novelty-induced decrease in horizontal and vertical activity rates. These results suggest that haloperidol blocks the reinforcing and locomotor-depressant effects of a novel environment in a free-choice preference test.

Original languageEnglish (US)
Pages (from-to)683-689
Number of pages7
JournalPharmacology, Biochemistry and Behavior
Volume32
Issue number3
DOIs
StatePublished - Mar 1989
Externally publishedYes

Keywords

  • Amphetamine
  • Haloperidol
  • Locomotor activity
  • Morphine
  • Naltrexone
  • Novelty
  • Place preference behavior

ASJC Scopus subject areas

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

Fingerprint Dive into the research topics of 'Novelty-induced place preference behavior in rats: Effects of opiate and dopaminergic drugs'. Together they form a unique fingerprint.

Cite this