Methadone analgesia in morphine-insensitive CXBK mice Journal Article


Authors: Chang, A.; Emmel, D. W.; Rossi, G. C.; Pasternak, G. W.
Article Title: Methadone analgesia in morphine-insensitive CXBK mice
Abstract: Methadone, a potent opioid analgesic, has long been considered a μ-opioid, based upon the similarities between its actions and those of morphine. This classification is supported by the sensitivity of methadone analgesia to the highly μ-opioid receptor-selective antagonist β-funaltrexamine. Yet, CXBK mice respond normally to methadone despite their insensitivity to systemic morphine, distinguishing between the receptor mechanisms of the two drugs. β-Funaltrexamine antagonizes methadone analgesia in CXBK mice, implying that the opioid is still acting through a μ-opioid receptor. These results reveal distinct analgesic mechanisms for morphine and methadone and provide further support for multiple subtypes of μ-opioid receptors.
Keywords: controlled study; nonhuman; mouse; animals; mice; animal experiment; animal model; drug resistance; methadone; morphine; analgesics, opioid; drug sensitivity; analgesia; mu opiate receptor; naloxone; opiate receptor; beta funaltrexamine; analgesic activity; receptor subtype; opiate antagonist; strain; subcutaneous drug administration; male; priority journal; article; μ-opioid receptor
Journal Title: European Journal of Pharmacology
Volume: 351
Issue: 2
ISSN: 0014-2999
Publisher: Elsevier B.V.  
Date Published: 1998-06-19
Start Page: 189
End Page: 191
Language: English
DOI: 10.1016/s0014-2999(98)00366-5
PUBMED: 9687002
PROVIDER: scopus
DOI/URL:
Notes: Article -- Export Date: 12 December 2016 -- Source: Scopus
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MSK Authors
  1. Grace Rossi
    61 Rossi
  2. Gavril W Pasternak
    414 Pasternak
  3. Albert H Chang
    19 Chang
  4. David W Emmel
    2 Emmel