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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1
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pubmed:dateCreated |
1985-1-22
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pubmed:abstractText |
Monoiodo [125I-Tyr3]-Neurotensin binding was studied in post mortem substantia nigra from 17 control and 15 parkinsonian subjects. Binding to individual homogenates was decreased by 58%, 49% and 26% at 0.36, 1.4, 5.5 M(-9) concentration of ligand, respectively. Saturation analysis using pooled substantia nigra demonstrated an almost complete loss of the high affinity component of the neurotensin receptor complex, yielding a 24% loss of the total binding capacity, with no alteration of the low affinity component. Similarly an important loss of binding was observed in monoiodo[125I-Tyr3]-Neurotensin autoradiograms of two substantia nigra from parkinsonian subjects. These results support the hypothesis of neurotensin receptors occurring on dopamine cell bodies and/or dendrites in human substantia nigra. Role of neurotensin may be of importance in the regulation of dopamine pathway involved in parkinsonism.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Nov
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pubmed:issn |
0006-291X
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
30
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pubmed:volume |
125
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
395-404
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:6095844-Aged,
pubmed-meshheading:6095844-Animals,
pubmed-meshheading:6095844-Humans,
pubmed-meshheading:6095844-Male,
pubmed-meshheading:6095844-Neurotensin,
pubmed-meshheading:6095844-Parkinson Disease,
pubmed-meshheading:6095844-Rats,
pubmed-meshheading:6095844-Rats, Inbred Strains,
pubmed-meshheading:6095844-Receptors, Neurotensin,
pubmed-meshheading:6095844-Receptors, Neurotransmitter,
pubmed-meshheading:6095844-Substantia Nigra,
pubmed-meshheading:6095844-Thermodynamics,
pubmed-meshheading:6095844-Time Factors
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pubmed:year |
1984
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pubmed:articleTitle |
Loss of high affinity neurotensin receptors in substantia nigra from parkinsonian subjects.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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