Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
5
pubmed:dateCreated
1993-11-29
pubmed:abstractText
Glutamic acid and glycine were quantified in cells and medium of cultured rostral rhombencephalic neurons derived from fetal rats. In the presence of 1 mM Mg2+, NMDA (50 microM) significantly stimulated (by 69%) release of newly synthesized 5-[3H]hydroxytryptamine ([3H]5-HT). D-2-Amino-5-phosphonopentanoate (AP-5; 50 microM) blocked the stimulatory effect of NMDA. AP-5 by itself inhibited [3H]5-HT release (by 25%), suggesting a tonic control of 5-HT by glutamate. In the absence of Mg2+, basal [3H]5-HT release was 60% higher as compared with release with Mg2+. AP-5 blocked the increased [3H]5-HT release observed without Mg2+, suggesting that this effect was due to the stimulation of NMDA receptors by endogenous glutamate. Glycine (100 microM) inhibited [3H]5-HT release in the absence of Mg2+. Strychnine (50 microM) blocked the inhibitory effect of glycine, indicating an action through strychnine-sensitive inhibitory glycine receptors. The [3H]5-HT release stimulated by NMDA was unaffected by glycine. In contrast, when tested in the presence of strychnine, glycine increased NMDA-evoked [3H]5-HT release (by 22%), and this effect was prevented by a selective antagonist of the NMDA-associated glycine receptor, 7-chlorokynurenate (100 microM). 7-Chlorokynurenate by itself induced a drastic decrease in [3H]5-HT release, indicating that under basal conditions these sites were stimulated by endogenous glycine. These results indicate that NMDA stimulated [3H]5-HT release in both the presence or absence of Mg2+. Use of selective antagonists allowed differentiation of a strychnine-sensitive glycine response (inhibition of [3H]5-HT release) from a 7-chlorokynurenate-sensitive response (potentiation of NMDA-evoked [3H]5-HT release).
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/2-amino-5-phosphopentanoic acid, http://linkedlifedata.com/resource/pubmed/chemical/7-chlorokynurenic acid, http://linkedlifedata.com/resource/pubmed/chemical/Glutamates, http://linkedlifedata.com/resource/pubmed/chemical/Glutamic Acid, http://linkedlifedata.com/resource/pubmed/chemical/Glycine, http://linkedlifedata.com/resource/pubmed/chemical/Kynurenic Acid, http://linkedlifedata.com/resource/pubmed/chemical/N-Methylaspartate, http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Glycine, http://linkedlifedata.com/resource/pubmed/chemical/Receptors, N-Methyl-D-Aspartate, http://linkedlifedata.com/resource/pubmed/chemical/Serotonin, http://linkedlifedata.com/resource/pubmed/chemical/Strychnine, http://linkedlifedata.com/resource/pubmed/chemical/Valine
pubmed:status
MEDLINE
pubmed:month
Nov
pubmed:issn
0022-3042
pubmed:author
pubmed:issnType
Print
pubmed:volume
61
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
1692-7
pubmed:dateRevised
2007-11-15
pubmed:meshHeading
pubmed-meshheading:7901329-Animals, pubmed-meshheading:7901329-Cells, Cultured, pubmed-meshheading:7901329-Embryo, Mammalian, pubmed-meshheading:7901329-Female, pubmed-meshheading:7901329-Gestational Age, pubmed-meshheading:7901329-Glutamates, pubmed-meshheading:7901329-Glutamic Acid, pubmed-meshheading:7901329-Glycine, pubmed-meshheading:7901329-Kinetics, pubmed-meshheading:7901329-Kynurenic Acid, pubmed-meshheading:7901329-N-Methylaspartate, pubmed-meshheading:7901329-Pregnancy, pubmed-meshheading:7901329-Raphe Nuclei, pubmed-meshheading:7901329-Rats, pubmed-meshheading:7901329-Rats, Sprague-Dawley, pubmed-meshheading:7901329-Receptors, Glycine, pubmed-meshheading:7901329-Receptors, N-Methyl-D-Aspartate, pubmed-meshheading:7901329-Rhombencephalon, pubmed-meshheading:7901329-Serotonin, pubmed-meshheading:7901329-Strychnine, pubmed-meshheading:7901329-Valine
pubmed:year
1993
pubmed:articleTitle
N-methyl-D-aspartic acid/glycine interactions on the control of 5-hydroxytryptamine release in raphe primary cultures.
pubmed:affiliation
Laboratoire de Neuroendocrinologie Expérimentale, INSERM U. 297, UER Faculté de Médecine-Nord, Marseille, France.
pubmed:publicationType
Journal Article