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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
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pubmed:dateCreated |
1992-12-22
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pubmed:abstractText |
We investigated the effect of the selective D1 dopamine antagonist, SCH23390, on the establishment of a pipradrol-conditioned place preference (CPP). Among various doses of pipradrol (6.25-75.0 mg/kg, SC), a CPP was established at 25.0 mg/kg. SCH23390 (0.16 mg/kg, IP) blocked the establishment of a CPP by this dose of pipradrol. The results suggest that pipradrol produces a rewarding effect and that this effect may involve activation of D1 dopamine receptors.
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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 |
Oct
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pubmed:issn |
0091-3057
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
43
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
377-80
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pubmed:dateRevised |
2008-11-21
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pubmed:meshHeading |
pubmed-meshheading:1359572-Animals,
pubmed-meshheading:1359572-Benzazepines,
pubmed-meshheading:1359572-Conditioning, Operant,
pubmed-meshheading:1359572-Male,
pubmed-meshheading:1359572-Piperidines,
pubmed-meshheading:1359572-Rats,
pubmed-meshheading:1359572-Receptors, Dopamine D1,
pubmed-meshheading:1359572-Reward
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pubmed:year |
1992
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pubmed:articleTitle |
Pipradrol conditioned place preference is blocked by SCH23390.
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pubmed:affiliation |
Department of Psychology, McGill University, Montreal, Quebec, Canada.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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