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dc.contributor.author Tuboly, Eszter
dc.contributor.author Gáspár, Renáta
dc.contributor.author Ibor, Miguel Olias
dc.contributor.author Gömöri, Kamilla
dc.contributor.author Kiss, Bernadett
dc.contributor.author Strifler, Gerda
dc.contributor.author Hartmann, Petra
dc.contributor.author Ferdinandy, Péter
dc.contributor.author Bartekova, Monika
dc.contributor.author Boros, Mihály
dc.contributor.author Görbe, Anikó
dc.date.accessioned 2019-12-04T15:25:33Z
dc.date.available 2019-12-04T15:25:33Z
dc.date.issued 2019
dc.identifier 85068839340
dc.identifier.citation journalVolume=460;journalIssueNumber=1-2;journalTitle=MOLECULAR AND CELLULAR BIOCHEMISTRY;pagerange=195-203;journalAbbreviatedTitle=MOL CELL BIOCHEM;
dc.identifier.uri http://repo.lib.semmelweis.hu//handle/123456789/7995
dc.identifier.uri doi:10.1007/s11010-019-03580-1
dc.description.abstract L-Alpha-glycerylphosphorylcholine (GPC) is a widely used food supplement. GPC has been shown to exert beneficial effects in several organs; however, the cardiac effects of GPC have yet to be investigated. The aim of the present study was therefore to map out the effects of GPC on cardiac myocytes, with or without ischemia-reperfusion insult. Neonatal rat cardiac myocytes were treated with GPC at 1, 10, 80, and 100 µM concentrations for 15 min, 3 h, or 24 h, respectively. Cell viability by calcein assay and the degree of oxidative stress by DHE (superoxide level) and H2DCF (total ROS accumulation) staining were measured. In separate experiments, cardiomyocytes were pre-treated with the optimal concentration of GPC for 3 h and then cells were exposed to 4 h of simulated ischemia followed by 2 h of reperfusion (SI/R). Cell viability was measured at the end of the SI/R protocol. In normoxic conditions, the 15-min and the 3-h GPC treatment did not affect cell viability, total ROS, and superoxide levels. Under SI/R conditions, the 3-h GPC treatment protected the cardiac myocytes from SI/R-induced cell death and did not alter the level of oxidative stress. The 24-h GPC treatment in normoxic conditions resulted in significant cell death and increased oxidative stress at each concentration. Here we provide the first evidence for the cytoprotective effect of short-term GPC treatment. However, long-term administration of GPC may exert cytotoxicity in a wide concentration range in cardiac myocytes. These results may draw attention to a comprehensive cardiac safety protocol for the testing of GPC.
dc.format.extent 195-203
dc.relation.ispartof urn:issn:0300-8177
dc.title L-Alpha-glycerylphosphorylcholine can be cytoprotective or cytotoxic in neonatal rat cardiac myocytes
dc.type Journal Article
dc.date.updated 2019-11-25T08:46:40Z
dc.language.rfc3066 en
dc.rights.holder NULL
dc.identifier.mtmt 30733384
dc.identifier.wos 000485970900016
dc.identifier.pubmed 31280435
dc.contributor.department SE/AOK/I/Farmakológiai és Farmakoterápiás Intézet
dc.contributor.institution Semmelweis Egyetem
dc.mtmt.swordnote Eszter Tuboly and Renáta Gáspár have contributed equally to this work.


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