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rdf:type | |
lifeskim:mentions |
umls-concept:C0013030,
umls-concept:C0030685,
umls-concept:C0035820,
umls-concept:C0085862,
umls-concept:C0086045,
umls-concept:C0220839,
umls-concept:C0391871,
umls-concept:C0680255,
umls-concept:C1159717,
umls-concept:C1283071,
umls-concept:C1299583,
umls-concept:C1519355,
umls-concept:C1549571,
umls-concept:C1555029,
umls-concept:C1608386,
umls-concept:C1963578
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pubmed:issue |
3
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pubmed:dateCreated |
1991-4-24
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pubmed:abstractText |
Glutamate stimulated the efflux of dopamine from slices of rat striatum superfused with a Krebs' bicarbonate buffer containing a physiological concentration of Mg++ (1.2 mM). This effect was observed in the presence of high concentrations of glutamate (3-10 mM), but not at lower concentrations (0.01-1 mM). The response was not accompanied by increased lactate dehydrogenase activity, a measure of glutamate neurotoxicity. At 10 mM, glutamate increased dopamine efflux by more than 9-fold. This was reduced to about 34% of the control response by either the competitive N-methyl-D-aspartate receptor antagonist 2-amino-5-phosphonovaleric acid (100 microM) or the noncompetitive N-methyl-D-aspartate receptor antagonist MK 801 [(+)-5-methyl-10,11-dihydro-5H-dibenso[a,d]cyclohepten-5,10- imine hydrogen maleate] (1-10 microM), but was unaffected by a kainate/quisqualate receptor antagonist 6-cyano-7-nitroquinoxaline-2,3-dione (10-100 microM). Glutamate-stimulated dopamine efflux also was unaffected by tetrodotoxin (0.5 microM), withdrawal of extracellular Ca++ [and addition of 1 mM ethylene glycol bis(beta-aminoethyl ether)-N,N'-tetraacetic acid] or systemic administration of reserpine (5 mg/kg, 24 hr before the experiment), an inhibitor of the vesicular storage of dopamine. In contrast, nomifensine (10 microM), an inhibitor of high-affinity dopamine transport, reduced glutamate-induced dopamine efflux to 15% of the control response. Moreover, the response to glutamate was blocked by deleting NaCl from the medium. Collectively, these results suggest that, at high concentrations and in the presence of Mg++, glutamate can stimulate the release of dopamine by a mechanism that does not use Ca(++)-dependent exocytosis but instead involves a reversal of the dopamine transport system.(ABSTRACT TRUNCATED AT 250 WORDS)
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Calcium,
http://linkedlifedata.com/resource/pubmed/chemical/Glutamates,
http://linkedlifedata.com/resource/pubmed/chemical/Glutamic Acid,
http://linkedlifedata.com/resource/pubmed/chemical/Magnesium,
http://linkedlifedata.com/resource/pubmed/chemical/Nomifensine,
http://linkedlifedata.com/resource/pubmed/chemical/Reserpine
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pubmed:status |
MEDLINE
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pubmed:month |
Mar
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pubmed:issn |
0022-3565
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
256
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1132-8
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pubmed:dateRevised |
2007-11-14
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pubmed:meshHeading |
pubmed-meshheading:1672376-Animals,
pubmed-meshheading:1672376-Calcium,
pubmed-meshheading:1672376-Chromatography, High Pressure Liquid,
pubmed-meshheading:1672376-Corpus Striatum,
pubmed-meshheading:1672376-Dopamine,
pubmed-meshheading:1672376-Glutamates,
pubmed-meshheading:1672376-Glutamic Acid,
pubmed-meshheading:1672376-Magnesium,
pubmed-meshheading:1672376-Male,
pubmed-meshheading:1672376-Nomifensine,
pubmed-meshheading:1672376-Rats,
pubmed-meshheading:1672376-Rats, Inbred Strains,
pubmed-meshheading:1672376-Reserpine
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pubmed:year |
1991
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pubmed:articleTitle |
High glutamate concentrations evoke Ca(++)-independent dopamine release from striatal slices: a possible role of reverse dopamine transport.
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pubmed:affiliation |
Department of Behavioral Neuroscience, University of Pittsburgh, Pennsylvania.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.
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