Linked Life Data

8787212

Source:http://linkedlifedata.com/resource/pubmed/id/8787212

Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
1
pubmed:dateCreated
1996-9-23
pubmed:abstractText
Ischemic neuronal injury is supposed to be caused in part by the extracellular accumulation of excitatory amino acids (EAA). Neurotransmitter and metabolic EAA can be released from synaptic vesicles and cytoplasm of neurones and glial cells. In this study the release of the glutamate analogue [3H]D-aspartate ([3H]D-ASP), loaded into 500 microns slices of rat hippocampus, was investigated. The efflux of the label was measured during anoxic-aglycemic ("ischemic") and normoxic K+ depolarization. To identify the pools from which [3H]D-ASP is released we have estimated its calcium dependence and the effects of inhibitors of: (1) Na(+)-dependent transporter of amino acids (100 microM L-trans-pyrrolidine-2,4-dicarboxylic acid/L-trans-PDC/), (2) sodium channel (1 microM tetrodotoxin TTX), and (3) anion channel (1 mM furosemide). [3H]D-ASP released upon normoxic depolarization was 40% inhibited by TTX, nearly 40% by L-trans-PDC and over 50% by furosemide. The "ischemic" release was in 40% calcium dependent, completely TTX independent and in approximately 50% blocked by furosemide treatment. Our data suggest that EAA accumulated in the synaptic cleft during ischemia are mainly released from the cytosolic compartment by mechanisms which are connected with the ischemic increase of extracellular potassium concentration.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:issn
0065-1400
pubmed:author
pubmed:issnType
Print
pubmed:volume
56
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
63-70
pubmed:dateRevised
2006-11-15
pubmed:meshHeading
pubmed:year
1996
pubmed:articleTitle
Enhancement of 3[H]D-aspartate release during ischemia like conditions in rat hippocampal slices: source of excitatory amino acids.
pubmed:affiliation
Department of Neurochemistry, Medical Research Centre, Polish Academy of Sciences, Warsaw, Poland.
pubmed:publicationType
Journal Article, In Vitro