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dc.contributor.authorTuran, Mehmet İbrahim
dc.contributor.authorTan, Hüseyin
dc.contributor.authorÇetin, Nihal
dc.contributor.authorSüleyman, Halis
dc.contributor.authorÇayır, Atilla
dc.date.accessioned2020-12-19T20:03:21Z
dc.date.available2020-12-19T20:03:21Z
dc.date.issued2014
dc.identifier.citationTuran, M.I., Tan, H., Cetin, N., Suleyman, H., Cayir, A. (2014). Effects of thiamine and thiamine pyrophosphate on epileptic episode model established with caffeine in rats. Epilepsy Research, 108(3), 405-410. https://doi.org/10.1016/j.eplepsyres.2013.12.006en_US
dc.identifier.issn0920-1211
dc.identifier.issn1872-6844
dc.identifier.urihttps://doi.org/10.1016/j.eplepsyres.2013.12.006
dc.identifier.urihttps://hdl.handle.net/11436/3150
dc.descriptionCetin, Nihal/0000-0003-3233-8009;en_US
dc.descriptionWOS: 000334476300006en_US
dc.descriptionPubMed: 24434003en_US
dc.description.abstractThis study examines the effect of thiamine (TH) and thiamine pyrophosphate (TPP) on epileptic episode model induced in rats with caffeine. Animals were divided into groups and given TH or TPP at doses of 10, 30 or 50 mg/kg intraperitoneally. Subsequently, all animal groups were injected intraperjtoneally with caffeine at a dose of 300 mg/kg. Time of onset of epileptic episode was recorded, and the latent period was calculated in seconds. At the end of the experiment, tGSH and MDA levels and SOD and MPO enzyme activities in extracted brain tissues were measured. Latent period duration in rats in the control group was 134 +/- 3.2 s, compared to 144 +/- 13.9, 147 +/- 14.5 and 169 +/- 15.1 s, respectively, in the TH10, TH30 and TH50 groups and 184 +/- 8.54, 197 +/- 9.1, 225 +/- 8.37 s, respectively, in the TPP10, TPP30 and TPP50 groups. Latent period duration was 236 +/- 6.7 in the diazepam group. Oxidant products were significantly lower in the TPP10, TPP30, TPP50 and diazepam groups compared to the control group (P < 0.05), while SOD activity and tGSH levels were significantly higher (P< 0.05). There was no significant difference between the TH10, TH30, TH50 groups and the control group in terms of oxidant and antioxidant levels (P > 0.05). in conclusions, TPP, especially at a dose of 50 mg/kg, significantly prolonged the latent period from administration of caffeine to time of episode and prevented oxidative damage. (C) 2013 Elsevier B.V. All rights reserved.en_US
dc.language.isoengen_US
dc.publisherElsevieren_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectRaten_US
dc.subjectSeizureen_US
dc.subjectThiamineen_US
dc.subjectThiamine pyrophosphateen_US
dc.subjectOxidanten_US
dc.titleEffects of thiamine and thiamine pyrophosphate on epileptic episode model established with caffeine in ratsen_US
dc.typearticleen_US
dc.contributor.departmentRTEÜ, Tıp Fakültesi, Dahili Tıp Bilimleri Bölümüen_US
dc.contributor.institutionauthorÇetin, Nihal
dc.contributor.institutionauthorSüleyman, Halis
dc.identifier.doi10.1016/j.eplepsyres.2013.12.006
dc.identifier.volume108en_US
dc.identifier.issue3en_US
dc.identifier.startpage405en_US
dc.identifier.endpage410en_US
dc.relation.journalEpilepsy Researchen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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