Autoradiographic localization of benzomorphan binding sites in rat brain
Author
dc.contributor.author
Crain, Barbara J.
Author
dc.contributor.author
Valdes, Fernando
Author
dc.contributor.author
Chang, Kwen Jen
Author
dc.contributor.author
McNamara, James O.
Admission date
dc.date.accessioned
2019-01-29T14:47:13Z
Available date
dc.date.available
2019-01-29T14:47:13Z
Publication date
dc.date.issued
1985
Cita de ítem
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European Journal of Pharmacology, Volumen 113, Issue 2, 2018, Pages 179-186
Identifier
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00142999
Identifier
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10.1016/0014-2999(85)90734-4
Identifier
dc.identifier.uri
https://repositorio.uchile.cl/handle/2250/160582
Abstract
dc.description.abstract
The benzomorphan subpopulation of opiate binding sites was labeled by [3H]diprenorphine in the presence of unlabeled ligands selected to quench μ and δ opiate binding sites. The distribution of benzomorphan binding sites was then localized autoradiographically. Areas particularly enriched in these sites were nucleus solitarius, nucleus ambiguus, substantia gelantinosa of the trigeminal nerve, the habenula, and the medial nucleus of the amygdala. Within hippocampal formation, binding was relatively enhanced in the pyramidal and granule cell layers. Within the basal ganglia, binding was greatest in the dorsomedial caudate nucleus and least in the globus pallidus. No 'patches' of increased binding were present in the striatum. The interstitial nucleus of the stria terminalis and the medial preoptic nucleus also showed significant binding. This distribution differs from the distributions of μ, δ and κ opiate binding and is quite similar to the distribution of β-endorphin immunoreactivity.