Reinforcing properties of morphine and naloxone revealed by conditioned place preferences: a procedural examination

Reinforcing properties of morphine and naloxone revealed by conditioned place preferences: a... 213 82 82 3 3 R. F. Mucha S. D. Iversen Department of Experimental Psychology University of Cambridge Downing Street CB2 3EB Cambridge UK Division of Neuropharmacology Max-Planck-Institute for Psychiatry Kraepelinstrasse 2 D-8000 Munich 40 RFG Abstract In rats, conditioned place preferences are produced by morphine and conditioned place aversions produced by naloxone. In the present studies, several issues concerning the demonstration and interpretation of place conditioning findings were examined in a two-compartment (black and white) tilt box: (1) the responses of naive rats to testing, (2) place conditioning in rats with strong unconditioned biases to one of the sides, and (3) modifications of the testing situation so that naive rats respond to the black and white sides with a minimum of initial bias. Experiments involving manipulation of the conditions of training and testing, use of pentobarbital, and use of a three-compartment test box helped to control for morphine's ability to produce state dependent learning as an explanation of its conditioned place preference. In addition, we examined previous place conditioning studies that failed to show aversive effects of naloxone. These negative findings were suggested to be due to the use or procedures insensitive to aversive stimuli and to the IP administration of naloxone. Finally, in the course of the experiments, novel data on general parameters of the place conditioning were provided. Dose-response curves for subcutaneous (SC) morphine (0.04–5.0 mg/kg) and naloxone (0.02–5.0 mg/kg) were established. Conditioned preferences were also shown to occur after at three pairings of SC drug, and they were retained for at least 1 month. http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.png Psychopharmacology Springer Journals

Reinforcing properties of morphine and naloxone revealed by conditioned place preferences: a procedural examination

Psychopharmacology, Volume 82 (3) – Sep 1, 1984

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Publisher
Springer Journals
Copyright
Copyright © 1984 by Springer-Verlag
Subject
Biomedicine; Pharmacology/Toxicology; Psychiatry
ISSN
0033-3158
eISSN
1432-2072
D.O.I.
10.1007/BF00427782
Publisher site
See Article on Publisher Site

Abstract

213 82 82 3 3 R. F. Mucha S. D. Iversen Department of Experimental Psychology University of Cambridge Downing Street CB2 3EB Cambridge UK Division of Neuropharmacology Max-Planck-Institute for Psychiatry Kraepelinstrasse 2 D-8000 Munich 40 RFG Abstract In rats, conditioned place preferences are produced by morphine and conditioned place aversions produced by naloxone. In the present studies, several issues concerning the demonstration and interpretation of place conditioning findings were examined in a two-compartment (black and white) tilt box: (1) the responses of naive rats to testing, (2) place conditioning in rats with strong unconditioned biases to one of the sides, and (3) modifications of the testing situation so that naive rats respond to the black and white sides with a minimum of initial bias. Experiments involving manipulation of the conditions of training and testing, use of pentobarbital, and use of a three-compartment test box helped to control for morphine's ability to produce state dependent learning as an explanation of its conditioned place preference. In addition, we examined previous place conditioning studies that failed to show aversive effects of naloxone. These negative findings were suggested to be due to the use or procedures insensitive to aversive stimuli and to the IP administration of naloxone. Finally, in the course of the experiments, novel data on general parameters of the place conditioning were provided. Dose-response curves for subcutaneous (SC) morphine (0.04–5.0 mg/kg) and naloxone (0.02–5.0 mg/kg) were established. Conditioned preferences were also shown to occur after at three pairings of SC drug, and they were retained for at least 1 month.

Journal

PsychopharmacologySpringer Journals

Published: Sep 1, 1984

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