Rat ventral midbrain dopamine neurons express the orphanin FQ/nociceptin receptor ORL-1

Neuroreport. 2002 Jul 2;13(9):1137-40. doi: 10.1097/00001756-200207020-00013.

Abstract

Orphanin FQ/nociceptin, (OFQ/N) the endogenous ligand for the ORL-1 receptor, has been shown previously to modulate extracellular dopamine concentration in the nucleus accumbens following both intracerebroventricular and intra-ventral tegmental area administration. However, it is unclear whether or not this is a result of a direct action of OFQ/N on ORL-1 receptors located on dopamine neurons. We sought evidence for expression of the ORL-1 receptor in dopamine cells located in the ventral tegmental area and substantia nigra of the rat brain using double-label in situ hybridization. Within the ventral tegmental area, 91% of tyrosine hydroxylase-positive cells were also positive for ORL-1 hybridization. Similarly, in the substantia nigra 90% of tyrosine hydroxylase-positive cells in the zona compacta expressed ORL-1 message and 84% of tyrosine hydroxylase-positive cells in the zona reticulata colocalized ORL-1 message. These data provide the anatomical basis for a direct modulatory effect of OFQ/N on mid-brain dopamine neurons.

Publication types

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

MeSH terms

  • Animals
  • Cell Count
  • Dopamine / metabolism*
  • In Situ Hybridization
  • Neural Pathways / cytology
  • Neural Pathways / metabolism
  • Neurons / cytology
  • Neurons / metabolism*
  • Nociceptin
  • Nociceptin Receptor
  • Nucleus Accumbens / cytology
  • Nucleus Accumbens / metabolism
  • Oligonucleotide Probes
  • Opioid Peptides / metabolism*
  • RNA, Messenger / metabolism
  • Rats
  • Rats, Sprague-Dawley
  • Receptors, Opioid / genetics*
  • Substantia Nigra / cytology
  • Substantia Nigra / metabolism*
  • Synaptic Transmission / physiology
  • Tyrosine 3-Monooxygenase / genetics
  • Ventral Tegmental Area / cytology
  • Ventral Tegmental Area / metabolism*

Substances

  • Oligonucleotide Probes
  • Opioid Peptides
  • RNA, Messenger
  • Receptors, Opioid
  • Tyrosine 3-Monooxygenase
  • Dopamine
  • Nociceptin Receptor
  • Oprl protein, rat