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, O.; Omurtag, G. Z.; Yurdun, T.
dc.date.accessioned2022-03-15T11:11:40Z
dc.date.accessioned2026-01-11T07:58:53Z
dc.date.available2022-03-15T11:11:40Z
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 mumol 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 micrograms/ml and 10.7 +/- 2.8 micrograms/ml, respectively.
dc.identifier.doi10.1515/dmdi.1998.14.4.251
dc.identifier.issn0792-5077
dc.identifier.pubmedPMID: 10694932
dc.identifier.urihttps://hdl.handle.net/11424/248955
dc.language.isoeng
dc.relation.ispartofDrug Metabolism and Drug Interactions
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectAnimals
dc.subjectMale
dc.subjectRats
dc.subjectRats, Wistar
dc.subjectGlutathione
dc.subjectLiver
dc.subjectAnticonvulsants
dc.subjectChromatography, High Pressure Liquid
dc.subjectCarbamazepine
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.startPage251
oaire.citation.titleDrug Metabolism and Drug Interactions
oaire.citation.volume4

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