Role of DRD3 in morphine-induced conditioned place preference using drd3-knockout mice

Neuroreport. 2004 Oct 5;15(14):2245-9. doi: 10.1097/00001756-200410050-00021.

Abstract

The dopamine D3 receptor (DRD3) mediates expression of conditioned effects of psychostimulants, but conflicting results have been obtained with opiates. In a conditioned place preference (CPP) procedure, morphine increased the time spent in a compartment previously paired with drug injection. CPP was obtained at morphine doses of 16 and 32 mg/kg in wild-type (drd3+/+) mice and 8, 16 and 32 mg/kg in DRD3-knockout (drd3-/-) mice. BP897, a DRD3-selective partial agonist, inhibited the expression of morphine-CPP in drd3+/+, but not drd3-/- mice. BP 897 reduced brain regional activation, measured by c-fos imaging after the CPP test session, in the somatosensory cortex of drd3+/+, but not drd3-/- mice. These results confirm the role of DRD3 in the expression of conditioned effects of morphine and the participation of the somatosensory cortex in these effects.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Conditioning, Psychological / drug effects
  • Conditioning, Psychological / physiology*
  • Dose-Response Relationship, Drug
  • Genotype
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Morphine / pharmacology*
  • Receptors, Dopamine D2 / biosynthesis
  • Receptors, Dopamine D2 / deficiency
  • Receptors, Dopamine D2 / genetics
  • Receptors, Dopamine D2 / physiology*
  • Receptors, Dopamine D3

Substances

  • Drd3 protein, mouse
  • Receptors, Dopamine D2
  • Receptors, Dopamine D3
  • Morphine