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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1-2
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pubmed:dateCreated |
1986-2-18
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pubmed:abstractText |
Fetal rat dopamine (DA) neurons were cultured in vitro for a 6-day period and transported, after redissociation, for 2 days prior to being grafted to the neostriatum of adult rats with 6-hydroxydopamine lesions of the ascending nigrostriatal pathway. In 2 of the 5 graft recipients that were tested for amphetamine-induced motor asymmetry, the grafts eliminated the lesion-induced turning behaviour within 3-6 weeks after transplantation. Fluorescence histochemistry revealed surviving grafts in all 6 recipients at 7 weeks after transplantation, containing between 42 and 125 DA neurons. The number of surviving DA neurons in the 3 non-compensated rats was below the minimum number of cells previously found to be necessary for functional effects on turning behaviour to occur.
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pubmed:grant | |
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 |
0304-3940
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
24
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pubmed:volume |
61
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
79-84
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pubmed:dateRevised |
2007-11-14
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pubmed:meshHeading |
pubmed-meshheading:3935983-Animals,
pubmed-meshheading:3935983-Brain Diseases,
pubmed-meshheading:3935983-Cells, Cultured,
pubmed-meshheading:3935983-Corpus Striatum,
pubmed-meshheading:3935983-Dopamine,
pubmed-meshheading:3935983-Female,
pubmed-meshheading:3935983-Fetus,
pubmed-meshheading:3935983-Hydroxydopamines,
pubmed-meshheading:3935983-Mesencephalon,
pubmed-meshheading:3935983-Neural Pathways,
pubmed-meshheading:3935983-Oxidopamine,
pubmed-meshheading:3935983-Rats,
pubmed-meshheading:3935983-Rats, Inbred Strains,
pubmed-meshheading:3935983-Substantia Nigra
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pubmed:year |
1985
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pubmed:articleTitle |
Survival of intracerebrally grafted rat dopamine neurons previously cultured in vitro.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.,
Research Support, Non-U.S. Gov't
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