Egyszerű nézet

dc.contributor.author Kertesz S
dc.contributor.author Szabo G
dc.contributor.author Udvari, Szabolcs
dc.contributor.author Lévay, György István
dc.contributor.author Mátyus, Péter
dc.contributor.author Hársing, László Gábor
dc.date.accessioned 2014-11-16T15:30:58Z
dc.date.available 2014-11-16T15:30:58Z
dc.date.issued 2013
dc.identifier 84871928555
dc.identifier.citation pagination=1-6; journalVolume=1492; journalTitle=BRAIN RESEARCH;
dc.identifier.uri http://repo.lib.semmelweis.hu//handle/123456789/358
dc.identifier.uri doi:10.1016/j.brainres.2012.11.025
dc.description.abstract We used isolated chicken retina to induce spreading depression by the glutamate receptor agonist N-methyl-d-aspartate. The N-methyl-d-aspartate- induced latency time of spreading depression was extended by the glycine B binding site competitive antagonist 7-chlorokynurenic acid. Addition of the glycine transporter type-1 inhibitors NFPS and Org-24461 reversed the inhibitory effect of 7-chlorokynurenic acid on N-methyl-d- aspartate-evoked spreading depression. The glycine uptake inhibitory activity of Org-24461, NFPS, and some newly synthesized analogs of NFPS was determined in CHO cells stably expressing human glycine transporter type-1b isoform. Compounds, which failed to inhibit glycine transporter type-1, also did not have effect on retinal spreading depression. These experiments indicate that the spreading depression model in chicken retina is a useful in vitro test to determine activity of glycine transporter type-1 inhibitors. In addition, our data serve further evidence for the role of glycine transporter type-1 in retinal neurotransmission and light processing. © 2012 Elsevier B.V.
dc.relation.ispartof urn:issn:0006-8993
dc.title Temporal alteration of spreading depression by the glycine transporter type-1 inhibitors NFPS and Org-24461 in chicken retina
dc.type Journal Article
dc.date.updated 2014-08-18T18:51:13Z
dc.language.rfc3066 en
dc.identifier.mtmt 2165087
dc.identifier.wos 000314321800001
dc.identifier.pubmed 23178696
dc.contributor.department SE/GYTK/Szerves Vegytani Intézet
dc.contributor.department SE/ETK2007/AEI/Morfológiai és Fiziológiai Tanszék
dc.contributor.department SE/AOK/I/Farmakológiai és Farmakoterápiás Intézet
dc.contributor.institution Semmelweis Egyetem


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