Buprenorphine antinociception is abolished, but naloxone-sensitive reward is retained, in μ-opioid receptor knockout mice

Soichiro Ide, Masabumi Minami, Masamichi Satoh, George R. Uhl, Ichiro Sora, Kazutaka Ikeda

Research output: Contribution to journalArticlepeer-review

Abstract

Buprenorphine is a relatively nonselective opioid receptor partial agonist that is used in the management of both pain and addiction. To improve understanding of the opioid receptor subtypes important for buprenorphine effects, we now report the results of our investigation on the roles of μ-, δ-, and κ-opioid receptors in antinociceptive responses and place preferences induced by buprenorphine. Buprenorphine antinociception, assessed by hot-plate and tail-flick tests, was significantly reduced in heterozygous μ-opioid receptor knockout (MOR-KO) mice and abolished in homozygous MOR-KO mice. In contrast, buprenorphine retained its ability to establish a conditioned place preference (CPP) in homozygous MOR-KO, although the magnitude of place preference was reduced as the number of copies of wild-type μ-opioid receptor genes was reduced. The remaining CPP of buprenorphine was abolished by pretreatment with the nonselective opioid antagonist naloxone, but only partially blocked by pretreatment with either the δ-selective opioid antagonist naltrindole or the κ-selective opioid antagonist norbinaltorphimine. These data, and biochemical confirmation of buprenorphine actions as a partial δ-, μ-, and κ-agonist, support the ideas that μ-opioid receptors mediate most of analgesic properties of buprenorphine, but that μ- and δ- and/or κ-opioid receptors are each involved in the rewarding effects of this drug.

Original languageEnglish (US)
Pages (from-to)1656-1663
Number of pages8
JournalNeuropsychopharmacology
Volume29
Issue number9
DOIs
StatePublished - Sep 2004
Externally publishedYes

Keywords

  • Antinociception
  • Buprenorphine
  • Detoxification
  • Knockout mice
  • Opioid receptor
  • Reward

ASJC Scopus subject areas

  • Pharmacology

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