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pubmed-article:20643531pubmed:abstractTextStatus epilepticus (SE) leads to upregulation of pro-inflammatory proteins including cyclooxygenase-2 (cox-2) which could be implicated in the epileptogenic process and epileptic seizures. Recent studies show that cox-2 can regulate expression of P-glycoprotein (P-gp) during epileptogenesis and epilepsy. P-gp could cause pharmacoresistance by reducing brain entry of anti-epileptic drugs such as phenytoin (PHT). Here we have investigated the effects of cox-2 inhibition on epileptogenesis, spontaneous seizures and PHT treatment in a rat model for temporal lobe epilepsy (TLE).lld:pubmed
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pubmed-article:20643531pubmed:authorpubmed-author:GorterJan AJAlld:pubmed
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pubmed-article:20643531pubmed:authorpubmed-author:HoltmanLindaLlld:pubmed
pubmed-article:20643531pubmed:copyrightInfoCopyright 2010 Elsevier B.V. All rights reserved.lld:pubmed
pubmed-article:20643531pubmed:issnTypeElectroniclld:pubmed
pubmed-article:20643531pubmed:volume91lld:pubmed
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pubmed-article:20643531pubmed:year2010lld:pubmed
pubmed-article:20643531pubmed:articleTitleCox-2 inhibition can lead to adverse effects in a rat model for temporal lobe epilepsy.lld:pubmed
pubmed-article:20643531pubmed:affiliationSwammerdam Institute for Life Sciences, Center for Neuroscience, University of Amsterdam, Science Park 904, 1098 XH Amsterdam, The Netherlands.lld:pubmed
pubmed-article:20643531pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:20643531pubmed:publicationTypeComparative Studylld:pubmed
pubmed-article:20643531pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed
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