Heroin-induced locomotion and mesolimbic dopamine release is unchanged in mice lacking the ORL.1 receptor gene

Brain Res. 2002 Oct 25;953(1-2):276-80. doi: 10.1016/s0006-8993(02)03398-x.

Abstract

We sought evidence for a role of endogenous nociceptin in modulating opiate effects on locomotion and mesolimbic dopamine release. Heroin administration (1, 3 and 10 mg/kg) induced dose-dependent increases in locomotion and mesolimbic dopamine release. However, no differences were identified between wild-type and nociceptin receptor-deficient mice, suggesting that either these systems are not influenced by an endogenous nociceptin tone, or that compensatory mechanisms activated during development normalize the response.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Analgesics, Opioid / pharmacology*
  • Animals
  • Dopamine / metabolism*
  • Heroin / pharmacology*
  • Limbic System / drug effects*
  • Limbic System / metabolism
  • Mice
  • Mice, Knockout
  • Motor Activity / drug effects
  • Nociceptin
  • Nociceptin Receptor
  • Opioid Peptides / physiology
  • Receptors, Opioid / genetics*

Substances

  • Analgesics, Opioid
  • Opioid Peptides
  • Receptors, Opioid
  • Heroin
  • Dopamine
  • Nociceptin Receptor
  • Oprl1 protein, mouse