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Opioid-NMDA receptor interactions may clarify conditioned (associative) components of opioid analgesic tolerance.

Abstract
Recent evidence suggests that acute administration of opioid analgesic drugs (such as morphine or heroin) produces delayed hyperalgesia. This hyperalgesic response is likely to result from hyperactivation of NMDA receptors triggered by stimulation of opioid receptors and may mediate acute tolerance. In support of this hypothesis, blockade of NMDA receptors attenuates opioid-induced delayed hyperalgesia and prolongs the duration of antinociceptive activity of morphine. Furthermore, the NMDA receptor-induced hyperalgesia is likely an unconditioned response to opioid receptor stimulation that becomes spatiotemporally associated with environmental cues accompanying repeated opioid exposure. This hypothesis conforms to the traditional Pavlovian requirement for conditioned and unconditioned responses to be qualitatively similar. In support of the role of NMDA receptor hyperactivation in morphine tolerance, NMDA receptor antagonists have been shown to block development of analgesic tolerance induced by repeated exposures to morphine. The view of the conditioned nature of opioid tolerance may be significantly extended by assuming that upon repeated drug administration an early-onset effect of a drug may become a predictive stimulus for a later-onset effect and, consequentially, it may become empowered to elicit the later-onset effect itself. Such 'intra-drug' conditioning hypothesis is well in line with the current experimental evidence but further studies will be needed to verify it directly.
AuthorsA Y Bespalov, E E Zvartau, P M Beardsley
JournalNeuroscience and biobehavioral reviews (Neurosci Biobehav Rev) Vol. 25 Issue 4 Pg. 343-53 (Jun 2001) ISSN: 0149-7634 [Print] United States
PMID11445139 (Publication Type: Journal Article, Review)
Chemical References
  • Analgesics, Opioid
  • Receptors, N-Methyl-D-Aspartate
  • Receptors, Opioid
Topics
  • Analgesics, Opioid (pharmacology)
  • Animals
  • Association Learning (drug effects)
  • Conditioning, Operant (drug effects)
  • Drug Tolerance
  • Receptors, N-Methyl-D-Aspartate (physiology)
  • Receptors, Opioid (physiology)

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