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| Predicate | Object |
|---|---|
| rdf:type | |
| lifeskim:mentions | |
| pubmed:issue |
6
|
| pubmed:dateCreated |
1981-2-24
|
| pubmed:abstractText |
The dipeptide gamma-D-glutamylglycine (gamma DGG) antagonizes amino acid-induced depolarization and synaptic excitation in the isolated hemisected spinal cord of the frog. In general, the effects of this compound resembled those of the structurally similar D-alpha-aminosuberate (D alpha AS) in being more effective against N-methyl-D-aspartate (NMDA)-induced responses than against responses induced by other excitatory amino acids. However gamma DGG appeared to be more effective than D alpha AS in depressing kainate-induced responses. Similar, though weaker, effects were produced by the L isomer of the dipeptide (gamma LGG), a natural brain constituent.
|
| pubmed:language |
eng
|
| pubmed:journal | |
| pubmed:citationSubset |
IM
|
| pubmed:chemical | |
| pubmed:status |
MEDLINE
|
| pubmed:month |
Dec
|
| pubmed:issn |
0022-3042
|
| pubmed:author | |
| pubmed:issnType |
Print
|
| pubmed:volume |
35
|
| pubmed:owner |
NLM
|
| pubmed:authorsComplete |
Y
|
| pubmed:pagination |
1458-60
|
| pubmed:dateRevised |
2006-11-15
|
| pubmed:meshHeading | |
| pubmed:year |
1980
|
| pubmed:articleTitle |
Dipeptide antagonists of amino acid-induced and synaptic excitation in the frog spinal cord.
|
| pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
|