Statements in which the resource exists.
SubjectPredicateObjectContext
pubmed-article:1505853rdf:typepubmed:Citationlld:pubmed
pubmed-article:1505853lifeskim:mentionsumls-concept:C0032659lld:lifeskim
pubmed-article:1505853lifeskim:mentionsumls-concept:C0162867lld:lifeskim
pubmed-article:1505853lifeskim:mentionsumls-concept:C0242184lld:lifeskim
pubmed-article:1505853lifeskim:mentionsumls-concept:C0017725lld:lifeskim
pubmed-article:1505853lifeskim:mentionsumls-concept:C1280500lld:lifeskim
pubmed-article:1505853lifeskim:mentionsumls-concept:C0205251lld:lifeskim
pubmed-article:1505853lifeskim:mentionsumls-concept:C0069772lld:lifeskim
pubmed-article:1505853lifeskim:mentionsumls-concept:C0547047lld:lifeskim
pubmed-article:1505853pubmed:issue3lld:pubmed
pubmed-article:1505853pubmed:dateCreated1992-9-21lld:pubmed
pubmed-article:1505853pubmed:abstractTextEvoked potentials were recorded in rat cerebral cortical slices. The amplitude of the evoked potential was reduced by perfusion with hypoxic (0-25%) or low glucose (0-5 mM) media in a concentration-dependent manner, and the evoked potentials disappeared under severe conditions (below 15% O2, below 3 mM glucose). We investigated the protective effects of oxiracetam on the decrease in evoked potentials under hypoxic (15% O2) and low glucose (3 mM glucose) conditions. Drugs were perfused from 45 min before hypoxic or low glucose perfusion to the end of the experiment. Oxiracetam (10(-6)-10(-5) M) dose-dependently minimized the amplitude reduction of evoked potentials and prolonged their disappearance time. At a concentration of 10(-5) M, oxiracetam protected against the disappearance of evoked potential in 5 of the 6 samples under hypoxic conditions and in all 6 samples under low glucose conditions. Indeloxazine (5 x 10(-6)-10(-5) M) and bifemelane (5 x 10(-6)-10(-5) M) prevented the reduction of the amplitude of evoked potentials under low glucose conditions. However, these drugs had no effect at a concentration of 10(-6) M. These data indicate that oxiracetam has a protective effect against neuronal dysfunction and that this effect develops at a lower concentration than those of indeloxazine and bifemelane.lld:pubmed
pubmed-article:1505853pubmed:languagejpnlld:pubmed
pubmed-article:1505853pubmed:journalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:1505853pubmed:citationSubsetIMlld:pubmed
pubmed-article:1505853pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:1505853pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:1505853pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:1505853pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:1505853pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:1505853pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:1505853pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:1505853pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:1505853pubmed:statusMEDLINElld:pubmed
pubmed-article:1505853pubmed:monthMarlld:pubmed
pubmed-article:1505853pubmed:issn0015-5691lld:pubmed
pubmed-article:1505853pubmed:authorpubmed-author:ShinodaYYlld:pubmed
pubmed-article:1505853pubmed:authorpubmed-author:HoriNNlld:pubmed
pubmed-article:1505853pubmed:authorpubmed-author:HokonoharaTTlld:pubmed
pubmed-article:1505853pubmed:issnTypePrintlld:pubmed
pubmed-article:1505853pubmed:volume99lld:pubmed
pubmed-article:1505853pubmed:ownerNLMlld:pubmed
pubmed-article:1505853pubmed:authorsCompleteYlld:pubmed
pubmed-article:1505853pubmed:pagination123-33lld:pubmed
pubmed-article:1505853pubmed:dateRevised2011-7-27lld:pubmed
pubmed-article:1505853pubmed:meshHeadingpubmed-meshheading:1505853-...lld:pubmed
pubmed-article:1505853pubmed:meshHeadingpubmed-meshheading:1505853-...lld:pubmed
pubmed-article:1505853pubmed:meshHeadingpubmed-meshheading:1505853-...lld:pubmed
pubmed-article:1505853pubmed:meshHeadingpubmed-meshheading:1505853-...lld:pubmed
pubmed-article:1505853pubmed:meshHeadingpubmed-meshheading:1505853-...lld:pubmed
pubmed-article:1505853pubmed:meshHeadingpubmed-meshheading:1505853-...lld:pubmed
pubmed-article:1505853pubmed:meshHeadingpubmed-meshheading:1505853-...lld:pubmed
pubmed-article:1505853pubmed:meshHeadingpubmed-meshheading:1505853-...lld:pubmed
pubmed-article:1505853pubmed:meshHeadingpubmed-meshheading:1505853-...lld:pubmed
pubmed-article:1505853pubmed:meshHeadingpubmed-meshheading:1505853-...lld:pubmed
pubmed-article:1505853pubmed:meshHeadingpubmed-meshheading:1505853-...lld:pubmed
pubmed-article:1505853pubmed:meshHeadingpubmed-meshheading:1505853-...lld:pubmed
pubmed-article:1505853pubmed:meshHeadingpubmed-meshheading:1505853-...lld:pubmed
pubmed-article:1505853pubmed:year1992lld:pubmed
pubmed-article:1505853pubmed:articleTitle[Effects of oxiracetam on the decrease in population spikes in hypoxic and low glucose media].lld:pubmed
pubmed-article:1505853pubmed:affiliationResearch Laboratories TOYO JOZO Co., Ltd., Shizuoka, Japan.lld:pubmed
pubmed-article:1505853pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:1505853pubmed:publicationTypeComparative Studylld:pubmed
pubmed-article:1505853pubmed:publicationTypeIn Vitrolld:pubmed
pubmed-article:1505853pubmed:publicationTypeEnglish Abstractlld:pubmed