Presence of opioid receptor-like (ORL1) receptor mRNA splice variants in peripheral sensory and sympathetic neuronal ganglia

Life Sci. 1999;64(22):2029-37. doi: 10.1016/s0024-3205(99)00150-2.

Abstract

The expression of ORL1 receptor mRNA splice variants is determined in peripheral sensory and sympathetic ganglia and compared to mRNA expression for the three classic opioid receptor subtypes (mu, delta, and kappa) using the method of reverse transcription-polymerase chain reaction. ORL1, mu, delta and kappa receptor subtype mRNAs are present in human dorsal root ganglia (DRG) and trigeminal ganglia and rat DRG. ORL1, mu and delta receptor subtype mRNAs are present in rat superior cervical ganglia and only ORL1 and delta receptor mRNAs are present in rat lumbar sympathetic ganglia. Both the ORL1 mRNA splice variants are present in sensory and sympathetic ganglia, however, expression of the shorter ORL1 receptor mRNA dominates over expression of the longer splice variant in rat brain and DRG, whereas, expression of the longer splice variant is dominant in sympathetic ganglia.

Publication types

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

MeSH terms

  • Aged
  • Animals
  • Base Sequence
  • Brain / metabolism
  • DNA Primers / genetics
  • Female
  • Ganglia, Sensory / metabolism*
  • Ganglia, Spinal / metabolism
  • Ganglia, Sympathetic / metabolism*
  • Genetic Variation
  • Humans
  • Male
  • Middle Aged
  • Nociceptin Receptor
  • RNA, Messenger / genetics*
  • RNA, Messenger / metabolism*
  • Rats
  • Rats, Sprague-Dawley
  • Receptors, Opioid / genetics*
  • Receptors, Opioid, delta / genetics
  • Receptors, Opioid, kappa / genetics
  • Receptors, Opioid, mu / genetics
  • Reverse Transcriptase Polymerase Chain Reaction
  • Superior Cervical Ganglion / metabolism
  • Trigeminal Ganglion / metabolism

Substances

  • DNA Primers
  • RNA, Messenger
  • Receptors, Opioid
  • Receptors, Opioid, delta
  • Receptors, Opioid, kappa
  • Receptors, Opioid, mu
  • Nociceptin Receptor