rdf:type |
|
lifeskim:mentions |
umls-concept:C0001041,
umls-concept:C0001792,
umls-concept:C0025260,
umls-concept:C0030685,
umls-concept:C0034693,
umls-concept:C0043047,
umls-concept:C0234112,
umls-concept:C0391871,
umls-concept:C0597198,
umls-concept:C0680255,
umls-concept:C0681842,
umls-concept:C1283071,
umls-concept:C1428114,
umls-concept:C1519355,
umls-concept:C1704240,
umls-concept:C1963578
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pubmed:issue |
8
|
pubmed:dateCreated |
2007-6-1
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pubmed:abstractText |
Cluster analysis of water-maze reference-memory performance distinguished subpopulations of young adult (3-5 months), aged (25-27 months) unimpaired (AU) and aged impaired (AI) rats. Working-memory performances of AU and AI rats were close to normal (though young and aged rats differed in exploration strategies). All aged rats showed impaired procedural-memory. Electrically evoked release of tritium was assessed in striatal slices (preloaded with [(3)H]choline) in the presence of oxotremorine, physostigmine, atropine+physostigmine, quinpirole, nomifensine or sulpiride. Aged rats exhibited reduced accumulation of [(3)H]choline (-30%) and weaker transmitter release. Drug effects (highest concentration) were reductions of release by 44% (oxotremorine), 72% (physostigmine), 84% (quinpirole) and 65% (nomifensine) regardless of age. Sulpiride and atropine+physostigmine facilitated the release more efficiently in young rats versus aged rats. The sulpiride-induced facilitation was weaker in AI rats versus AU rats; it significantly correlated with reference-memory performance. The results confirm age-related alterations of cholinergic and dopaminergic striatal functions, and point to the possibility that alterations in the D(2)-mediated dopaminergic regulation of these functions contribute to age-related reference-memory deficits.
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pubmed:language |
eng
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pubmed:journal |
|
pubmed:citationSubset |
IM
|
pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Acetylcholine,
http://linkedlifedata.com/resource/pubmed/chemical/Cholinesterase Inhibitors,
http://linkedlifedata.com/resource/pubmed/chemical/Dopamine Agonists,
http://linkedlifedata.com/resource/pubmed/chemical/Dopamine Antagonists,
http://linkedlifedata.com/resource/pubmed/chemical/Dopamine Uptake Inhibitors,
http://linkedlifedata.com/resource/pubmed/chemical/Muscarinic Agonists,
http://linkedlifedata.com/resource/pubmed/chemical/Nomifensine,
http://linkedlifedata.com/resource/pubmed/chemical/Oxotremorine,
http://linkedlifedata.com/resource/pubmed/chemical/Physostigmine,
http://linkedlifedata.com/resource/pubmed/chemical/Quinpirole,
http://linkedlifedata.com/resource/pubmed/chemical/Sulpiride
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pubmed:status |
MEDLINE
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pubmed:month |
Aug
|
pubmed:issn |
1558-1497
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pubmed:author |
|
pubmed:issnType |
Electronic
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pubmed:volume |
28
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pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
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pubmed:pagination |
1270-85
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pubmed:meshHeading |
pubmed-meshheading:16843572-Acetylcholine,
pubmed-meshheading:16843572-Age Factors,
pubmed-meshheading:16843572-Aging,
pubmed-meshheading:16843572-Animals,
pubmed-meshheading:16843572-Behavior, Animal,
pubmed-meshheading:16843572-Cholinesterase Inhibitors,
pubmed-meshheading:16843572-Corpus Striatum,
pubmed-meshheading:16843572-Dopamine Agonists,
pubmed-meshheading:16843572-Dopamine Antagonists,
pubmed-meshheading:16843572-Dopamine Uptake Inhibitors,
pubmed-meshheading:16843572-Electric Stimulation,
pubmed-meshheading:16843572-Female,
pubmed-meshheading:16843572-Maze Learning,
pubmed-meshheading:16843572-Memory,
pubmed-meshheading:16843572-Muscarinic Agonists,
pubmed-meshheading:16843572-Nomifensine,
pubmed-meshheading:16843572-Oxotremorine,
pubmed-meshheading:16843572-Physostigmine,
pubmed-meshheading:16843572-Quinpirole,
pubmed-meshheading:16843572-Rats,
pubmed-meshheading:16843572-Rats, Long-Evans,
pubmed-meshheading:16843572-Sulpiride
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pubmed:year |
2007
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pubmed:articleTitle |
Spatial reference- (not working- or procedural-) memory performance of aged rats in the water maze predicts the magnitude of sulpiride-induced facilitation of acetylcholine release by striatal slices.
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pubmed:affiliation |
Laboratoire de Neurosciences Comportementales et Cognitives, FRE 2855, CNRS-Université Louis Pasteur, IFR 37 Neurosciences, GDR CNRS 2905, Strasbourg, France. jean-christophe.cassel@psycho-ulp.u-strasbg.fr
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pubmed:publicationType |
Journal Article,
In Vitro,
Research Support, Non-U.S. Gov't
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