Morphine self-administration in mu-opioid receptor-deficient mice

Naunyn Schmiedebergs Arch Pharmacol. 2000 Jun;361(6):584-9. doi: 10.1007/s002100000244.

Abstract

Morphine-induced place preference was demonstrated recently in wild-type mice, whereas this conditioned behaviour was not observed in mu-opioid receptor-deficient mice. In the present study, we investigated locomotor effects of subcutaneously (s.c.) injected morphine as well as intracerebroventricular (i.c.v.) morphine self-administration in mu-opioid receptor-knockout mice. After s.c. morphine injection, locomotor activity significantly increased in wild-type animals. As expected, in the self-administration test the rate of self-administration constantly increased in wild-type mice reflecting reward effects of morphine. This increase was independent of locomotor/motor activity. In contrast, self-administration rates and locomotor/motor activity significantly decreased in the receptor-deficient animals. It was shown that this aversive effect might partly be due to kappa-opioid receptor interaction.

MeSH terms

  • Analysis of Variance
  • Animals
  • Autoradiography
  • Corpus Striatum / metabolism
  • Dose-Response Relationship, Drug
  • Enkephalin, Ala(2)-MePhe(4)-Gly(5)- / metabolism
  • Exploratory Behavior / drug effects
  • Hippocampus / metabolism
  • Injections, Intraventricular
  • Mice
  • Mice, Knockout
  • Morphine / administration & dosage
  • Morphine / pharmacology*
  • Motor Activity / drug effects*
  • Radioligand Assay
  • Random Allocation
  • Receptors, Opioid, kappa / antagonists & inhibitors
  • Receptors, Opioid, mu / genetics
  • Receptors, Opioid, mu / metabolism*
  • Self Administration

Substances

  • Receptors, Opioid, kappa
  • Receptors, Opioid, mu
  • Enkephalin, Ala(2)-MePhe(4)-Gly(5)-
  • Morphine