La maladie de Parkinson en France (serveur d'exploration)

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Regional distribution of μ, δ and κ opioid receptors in human brains from controls and parkinsonian subjects

Identifieur interne : 000854 ( Istex/Corpus ); précédent : 000853; suivant : 000855

Regional distribution of μ, δ and κ opioid receptors in human brains from controls and parkinsonian subjects

Auteurs : P. Delay-Goyet ; J.-M. Zajac ; F. Javoy-Agid ; Y. Agid ; B. P. Roques

Source :

RBID : ISTEX:EDD390816A43E3D1CC016367C64F5C952B9B9ECE

English descriptors

Abstract

Abstract: The binding properties of μ and δ opioid receptors were investigated in several areas of human brain by using [3H]Tyr-d-Ala-Gly-(Me)Phe-Gly-ol and [3H]Tyr-d-Thr-Gly-Phe-Leu-Thr as respective selective ligands, while the totality of opioid receptors was measured by using [3H]etorphine as a non-selective agonist. Receptor densities were highest in cerebral cortex, amygdala and striatum, and lowest in the substantia nigra (pars compacta). In the different brain areas of patients with Parkinson's disease, the density and the proportion of the various opioid receptors were not significantly different from control subjects.

Url:
DOI: 10.1016/0006-8993(87)91321-7

Links to Exploration step

ISTEX:EDD390816A43E3D1CC016367C64F5C952B9B9ECE

Le document en format XML

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<affiliation>De´partement de Chimie Organique, U.266 INSERM, U.A. 498 C.N.R.S., U.E.R. des Sciences Pharmaceutiques et Biologiques, Paris ,France</affiliation>
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<namePart type="given">J.-M.</namePart>
<namePart type="family">Zajac</namePart>
<affiliation>De´partement de Chimie Organique, U.266 INSERM, U.A. 498 C.N.R.S., U.E.R. des Sciences Pharmaceutiques et Biologiques, Paris ,France</affiliation>
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<name type="personal">
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<namePart type="family">Javoy-Agid</namePart>
<affiliation>Laboratoire de Me´decine Expe´rimentale, U.289 INSERM, U.E.R. Pitie´-Salpeˆtrie`re, Paris ,France</affiliation>
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<affiliation>Laboratoire de Me´decine Expe´rimentale, U.289 INSERM, U.E.R. Pitie´-Salpeˆtrie`re, Paris ,France</affiliation>
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<roleTerm type="text">author</roleTerm>
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<name type="personal">
<namePart type="given">B.P.</namePart>
<namePart type="family">Roques</namePart>
<affiliation>Correspondence: B.P. Roques, De´partement de Chimie Organique, U.266 INSERM, U.A. 498 C.N.R.S., U.E.R. des Sciences Pharmaceutiques et Biologiques, 4 Avenue de l'Observatoire, 75006 Paris ,France</affiliation>
<affiliation>De´partement de Chimie Organique, U.266 INSERM, U.A. 498 C.N.R.S., U.E.R. des Sciences Pharmaceutiques et Biologiques, Paris ,France</affiliation>
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<dateIssued encoding="w3cdtf">1987</dateIssued>
<copyrightDate encoding="w3cdtf">1987</copyrightDate>
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<abstract lang="en">Abstract: The binding properties of μ and δ opioid receptors were investigated in several areas of human brain by using [3H]Tyr-d-Ala-Gly-(Me)Phe-Gly-ol and [3H]Tyr-d-Thr-Gly-Phe-Leu-Thr as respective selective ligands, while the totality of opioid receptors was measured by using [3H]etorphine as a non-selective agonist. Receptor densities were highest in cerebral cortex, amygdala and striatum, and lowest in the substantia nigra (pars compacta). In the different brain areas of patients with Parkinson's disease, the density and the proportion of the various opioid receptors were not significantly different from control subjects.</abstract>
<subject lang="en">
<genre>Keywords</genre>
<topic>Opioid receptor</topic>
<topic>Selective ligand</topic>
<topic>δ-Enkephalin analogue</topic>
<topic>Discriminative binding property</topic>
<topic>Parkinson's disease</topic>
<topic>Human brain</topic>
</subject>
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<titleInfo>
<title>Brain Research</title>
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<titleInfo type="abbreviated">
<title>BRES</title>
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<genre type="journal">journal</genre>
<originInfo>
<dateIssued encoding="w3cdtf">19870623</dateIssued>
</originInfo>
<identifier type="ISSN">0006-8993</identifier>
<identifier type="PII">S0006-8993(00)X1162-6</identifier>
<part>
<date>19870623</date>
<detail type="volume">
<number>414</number>
<caption>vol.</caption>
</detail>
<detail type="issue">
<number>1</number>
<caption>no.</caption>
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<extent unit="issue pages">
<start>1</start>
<end>204</end>
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<extent unit="pages">
<start>8</start>
<end>14</end>
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<identifier type="istex">EDD390816A43E3D1CC016367C64F5C952B9B9ECE</identifier>
<identifier type="DOI">10.1016/0006-8993(87)91321-7</identifier>
<identifier type="PII">0006-8993(87)91321-7</identifier>
<identifier type="ArticleID">87913217</identifier>
<accessCondition type="use and reproduction" contentType="copyright">©1987 Elsevier Science Publishers B.V. (Biomedical Division)</accessCondition>
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