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Intrathecal administration of p-hydroxymercuribenzoate or phosphoramidon/bestatin-combined induces antinociceptive effects through different opioid mechanisms
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1998 (English)In: Neuropeptides, ISSN 0143-4179, E-ISSN 1532-2785, Vol. 32, no 5, 411-415 p.Article in journal (Refereed) Published
Abstract [en]

The antinociceptive effect of intrathecally (i.t.) administered protease inhibitors was tested against capsaicin (800 ng) injected into the dorsal surface of a hindpaw. Both p-hydroxymercuribenzoate (2-8 nmol), a cysteine protease inhibitor, and phosphoramidon (1-4 nmol), an endopeptidase 24.11 inhibitor in the presence of bestatin (0.25 nmol) an aminopeptidase inhibitor, administered i.t. 60 min prior to the injection of capsaicin produced a dose-dependent reduction of the capsaicin-induced paw licking and biting response. p-Hydroxymercuribenzoate (4 nmol)-induced antinociception was significantly antagonized by nor-binaltorphimine, a selective kappa-opioid receptor antagonist, but not by naltrindole, a selective delta-opioid receptor antagonist. On the other hand, phosphoramidon (4 nmol) /bestatin-induced antinociception was significantly antagonized by naltrindole, but not by nor-binaltorphimine. The results indicate that the antinociceptive effect of p-hydroxymercuribenzoate may be due to the inhibition of a cysteine protease degrading endogenous dynorphins whereas phosphoramidon in the presence of bestatin blocks the degradation of enkephalins.

Place, publisher, year, edition, pages
1998. Vol. 32, no 5, 411-415 p.
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Medical and Health Sciences Pharmaceutical Sciences
URN: urn:nbn:se:uu:diva-50736DOI: 10.1016/S0143-4179(98)90064-6ISI: 000076801500003PubMedID: 9845000OAI: oai:DiVA.org:uu-50736DiVA: diva2:78645
Available from: 2008-10-17 Created: 2008-10-17 Last updated: 2011-03-10Bibliographically approved

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Nylander, Ingrid
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