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Exploring delta-receptor function using the selective opioid antagonist naltrindole.

作者信息

Jackson H C, Ripley T L, Nutt D J

机构信息

Reckitt and Colman Psychopharmacology Unit, School of Medical Sciences, Bristol, England.

出版信息

Neuropharmacology. 1989 Dec;28(12):1427-30. doi: 10.1016/0028-3908(89)90022-1.

DOI:10.1016/0028-3908(89)90022-1
PMID:2559353
Abstract

Until recently the only pharmacological probes for delta-receptors have been peptide enkephalin analogues. These suffer from a number of limitations including high cost, partial agonist effects and a propensity for neurotoxicity. A stable non-peptide antagonist, naltrindole, has recently become available. We have explored its intrinsic actions and found that it attenuated swim stress-induced antinociception, a model for endogenous delta-receptor activation. Naltrindole may therefore be a useful alternative to presently available delta-receptor antagonists.

摘要

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Exploring delta-receptor function using the selective opioid antagonist naltrindole.
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