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Pharmacology of sucrose-reinforced place-preference conditioning: Effects of naltrexone

  • Andrew R. Delamater
  • , Anthony Sclafani
  • , Richard J. Bodnar

Research output: Contribution to journalArticlepeer-review

49 Scopus citations

Abstract

Two experiments investigated the role of the opioid system in sucrose-reinforced conditioned place preferences (CPPs) in rats. Experiment 1 examined the effects of a general opioid antagonist, naltrexone, on the expression of a CPP acquired in the absence of the drug. Subjects were trained to associate one compartment of a two-compartment chamber with sucrose and the other compartment with water. Rats displayed a preference for the sucrose-associated compartment in a choice test without sugar or water available following vehicle saline treatment. Naltrexone doses of 2.5 and 5.0 mg/kg reduced this preference for the sucrose-associated compartment. Experiment 2 examined the effects of naltrexone on the acquisition as well as the expression of CPPS. Different groups of rats received daily injections of either saline, 0.1, 1.0, or 5.0 mg/kg of naltrexone prior to each training session, and then these groups were given a choice test for the CPP after saline or naltrexone injections. Although naltrexone treatment attenuated the expression of CPPs in each group relative to saline treatment, there were no group differences during these tests in the magnitude of the preferences. Moreover, all groups displayed equal acquisition of CPPs despite the fact that naltrexone dose dependently decreased sucrose intake during the training phase. Together, the results indicate that the opioid system modulates the expression but not the acquisition of sucrose-reinforced CPPs. Copyright (C) 2000 Elsevier Science Inc.

Original languageEnglish
Pages (from-to)697-704
Number of pages8
JournalPharmacology Biochemistry and Behavior
Volume65
Issue number4
DOIs
StatePublished - Apr 2000
Externally publishedYes

Keywords

  • Acquisition
  • Conditioned place preference
  • Expression
  • Naltrexone
  • Opioids
  • Sucrose

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