Functional antagonism of morphine analgesia by (+)-pentazocine: evidence for an anti-opioid sigma 1 system

Eur J Pharmacol. 1993 Nov 30;250(1):R7-8. doi: 10.1016/0014-2999(93)90650-7.

Abstract

Both (+)-pentazocine and (-)-pentazocine antagonize morphine analgesia equally well. This lack of stereospecificity implies an non-opioid mechanism of action. The antagonism of morphine analgesia by (+)-pentazocine is reversed by haloperidol, a potent dopamine D2 and sigma receptor antagonist. The inactivity of the highly selective dopamine D2 receptor antagonist (-)-sulpiride indicates that both (+)-pentazocine and haloperidol are acting through sigma receptors. Haloperidol, but not (-)-sulpiride, also enhances morphine analgesia. Together, these results suggest the presence of a tonically active anti-opioid sigma system within the brain.

Publication types

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

MeSH terms

  • Analgesia
  • Animals
  • Dopamine D2 Receptor Antagonists
  • Drug Interactions
  • Haloperidol / pharmacology
  • Male
  • Mice
  • Morphine / antagonists & inhibitors*
  • Pentazocine / pharmacology*
  • Receptors, sigma / antagonists & inhibitors
  • Receptors, sigma / drug effects
  • Receptors, sigma / physiology*
  • Stereoisomerism
  • Sulpiride / pharmacology

Substances

  • Dopamine D2 Receptor Antagonists
  • Receptors, sigma
  • Morphine
  • Sulpiride
  • Haloperidol
  • Pentazocine