Lack of cross-tolerance between U69,593 and bremazocine suggest κ-opioid receptor multiplicity in mice

Peter J. Horan, Frank Porreca

Research output: Contribution to journalArticle

19 Scopus citations

Abstract

The development of tolerance, and the possibility of cross-tolerance, to the κ-opioid receptor-mediated antinociceptive effects of U69,593 and bremazocine was studied in mice. U69,593 and bremazocine elicited dose-related and κ-receptor-mediated antinociception following i.c.v. administration to mice. After a 3 day treatment regimen (twice daily injections) with an approximate antinociceptive A90 dose (90 nmol, i.c.v.) of U69,593, tolerance developed as demonstrated by a 5.6-fold righrward shift of the U69,593 dose-response line. The i.c.v. dose-response line for bremazocine was unaltered in U69,593-tolerant mice. Pretreatment with an approximate antinociceptive A90 dose of bremazocine (30 nmol, i.c.v.) for 3 days also produced tolerance as shown by a greater than 15-fold rightward shift in the bremazocine antinociceptive dose-response line. The i.c.v. dose-response line for U69,593 was unaltered in bremazocine-tolerant mice. These data demonstrate that while tolerance develops to the antinociceptive effects of both U69,593 and bremazocine, a two-way lack of cross-tolerance can be demonstrated between these κ-agonists in this endpoint. These data suggest mechanistic differences in the antinociceptive effects of these κ-agonists. Such suggestions are consistent with antinociceptive action of these agonists at subtypes of κ-receptors.

Original languageEnglish (US)
Pages (from-to)93-98
Number of pages6
JournalEuropean Journal of Pharmacology
Volume239
Issue number1-3
DOIs
StatePublished - Aug 3 1993

Keywords

  • (Mouse)
  • Antinociception
  • Arylacetamides
  • Benzomorphans
  • κ-Opioid receptors

ASJC Scopus subject areas

  • Pharmacology

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