Tonic endogenous opioid inhibition of visceral noxious information in rabbits

Gastroenterology. 1996 Jul;111(1):78-84. doi: 10.1053/gast.1996.v111.pm8698228.

Abstract

Background & aims: A tonic intrinsic spinal inhibitory system on spinal motor reflexes in rabbits has been shown earlier. The aim of this study was to examine the effects of different opioid antagonists against visceral noxious stimulation in awake rabbits.

Methods: The opioid receptor antagonists examined were naloxone (nonselective), MR2266 (kappa), and naltrindole (delta). The effects on the visceromotor response thresholds induced by colorectal distention in rabbits were determined after intrathecal and intramuscular administration of the antagonists.

Results: Intrathecal naloxone resulted in a dose-dependent decrease of visceromotor response thresholds. The selective antagonists MR2266 and naltrindole had no significant effects. In the presence of MR2266, intrathecal naloxone reduced thresholds to the same degree as when given alone. Analysis of the data from all rabbits showed a statistically significant reduction in visceromotor response thresholds after intrathecal naloxone compared with intramuscular administration.

Conclusions: In rabbits, tonic active intrinsic spinal and supraspinal endogenous opioids modulate visceral noxious information. This inhibition is exerted at the mu opioid receptor.

Publication types

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

MeSH terms

  • Age Factors
  • Animals
  • Benzomorphans / administration & dosage
  • Benzomorphans / pharmacology
  • Dose-Response Relationship, Drug
  • Female
  • Gastrointestinal Motility / drug effects*
  • Injections, Intramuscular
  • Injections, Spinal
  • Naloxone / administration & dosage
  • Naloxone / pharmacology
  • Naltrexone / administration & dosage
  • Naltrexone / analogs & derivatives
  • Naltrexone / pharmacology
  • Narcotic Antagonists / administration & dosage
  • Narcotic Antagonists / pharmacology*
  • Opioid Peptides / antagonists & inhibitors*
  • Opioid Peptides / physiology
  • Rabbits
  • Receptors, Opioid / physiology

Substances

  • Benzomorphans
  • Narcotic Antagonists
  • Opioid Peptides
  • Receptors, Opioid
  • Naloxone
  • MR 2266
  • Naltrexone
  • naltrindole