Publication:
Effects of carbamazepine on hepatic glutathione level in rats and determination of carbamazepine and its epoxide metabolite in plasma by HPLC

dc.contributor.authorsYeşilaltay A.K., Ersoy Ö., Omurtag G.Z., Yurdun T.
dc.date.accessioned2022-03-15T01:53:37Z
dc.date.accessioned2026-01-10T20:28:40Z
dc.date.available2022-03-15T01:53:37Z
dc.date.issued1998
dc.description.abstractWe investigated whether carbamazepine, which is known to be metabolized to an electrophilic epoxide derivative in the body, causes any decrease, analogous to the action of epoxides, of hepatic glutathione (GSH) level in rats. Carbamazepine was administered to rats and liver GSH levels were determined spectrophotometrically. Neither a single low nor repeated low doses (30 mg/kg) of carbamazepine (CBZ) produced a statistically significant difference in GSH levels relative to controls. A single high dose of CBZ (100 mg/kg) produced a large and significant decrease relative to control (GSH level 3.82 ± 0.64 vs 6.54 ± 0.45 μmol GSH/g liver). CBZ and its metabolite carbamazepine-10,11-epoxide were determined in plasma by HPLC after the high dose of carbamazepine administration. The concentrations of carbamazepine and carbamazepine-10,11-epoxide were 18.9 ± 2.9 μg/ml and 10.7 ± 2.8 μg/ml, respectively.
dc.identifier.doi10.1515/DMDI.1998.14.4.251
dc.identifier.issn7925077
dc.identifier.pubmed10694932
dc.identifier.urihttps://hdl.handle.net/11424/246368
dc.language.isoeng
dc.publisherWalter de Gruyter GmbH
dc.relation.ispartofDrug Metabolism and Drug Interactions
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectCarbamazepine
dc.subjectCarbamazepine-10,11-epoxide
dc.subjectGlutathione
dc.subjectHPLC
dc.subjectLiver
dc.titleEffects of carbamazepine on hepatic glutathione level in rats and determination of carbamazepine and its epoxide metabolite in plasma by HPLC
dc.typearticle
dspace.entity.typePublication
oaire.citation.endPage258
oaire.citation.issue4
oaire.citation.startPage251
oaire.citation.titleDrug Metabolism and Drug Interactions
oaire.citation.volume14

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