Modifications of drug metabolism by disulfiram and diethyldithiocarbamate. II. D-Glucuronic acid pathway

dc.contributor.authorMarselos, M.en
dc.contributor.authorLang, M.en
dc.contributor.authorTorronen, R.en
dc.date.accessioned2015-11-24T19:04:11Z
dc.date.available2015-11-24T19:04:11Z
dc.identifier.issn0009-2797-
dc.identifier.urihttps://olympias.lib.uoi.gr/jspui/handle/123456789/19989
dc.rightsDefault Licence-
dc.subjectAlcohol Oxidoreductases/metabolismen
dc.subjectAnimalsen
dc.subjectDisulfiram/*pharmacologyen
dc.subjectDitiocarb/*pharmacologyen
dc.subjectFemaleen
dc.subjectGlucosephosphate Dehydrogenase/metabolismen
dc.subjectGlucuronates/*metabolismen
dc.subjectGlucuronidase/metabolismen
dc.subjectGlucuronosyltransferase/metabolismen
dc.subjectLiver/drug effects/*enzymologyen
dc.subjectPhenobarbital/pharmacologyen
dc.subjectPyrophosphatases/metabolismen
dc.subjectRatsen
dc.subjectSugar Acidsen
dc.subjectThiocarbamates/*pharmacologyen
dc.subjectUridine Diphosphate Glucose Dehydrogenase/metabolismen
dc.subjectUridine Diphosphate Glucuronic Aciden
dc.titleModifications of drug metabolism by disulfiram and diethyldithiocarbamate. II. D-Glucuronic acid pathwayen
heal.abstractHepatic enzymes connected with the formation and metabolism of free D-glucuronic acid were affected in rats after treatment with disulfiram or diethyldithiocarbamate (300 mg/kg, intragastrically, per day, 4 X). The activities of UDPglucose dehydrogenase, UDPglucuronic acid pyrophosphatase, UDPglucuronosyltransferase and L-gulonate dehydrogenase were enhanced, while those of glucose-6-phosphate dehydrogenase, beta-glucuronidase and D-glucuronolactone dehydrogenase were inhibited. These changes were more pronounced with disulfiram than diethyldithiocarbamate. Treatment with phenobarbital (80 mg/kg, i.p., per day, 4 X) enhanced UDP glucuronosyl-transferase, but brought about different effects on the other enzymes. Concurrent administration of phenobarbital with disulfiram or diethyldithiocarbamate led to potentiation or antagonism of the primary effects of each compound when given alone. The results suggest that activation of the D-glucuronic acid pathway may proceed in various ways, and that it is not necessarily followed by a simultaneous induction of the microsomal mixed-function oxygenase activity.en
heal.accesscampus-
heal.fullTextAvailabilityTRUE-
heal.identifier.secondaryhttp://www.ncbi.nlm.nih.gov/pubmed/187353-
heal.identifier.secondaryhttp://ac.els-cdn.com/0009279776901538/1-s2.0-0009279776901538-main.pdf?_tid=c368daeb54f5eb6c3a434c7893fe07a9&acdnat=1332744205_035b04cd04fbe84891786c6874410ce8-
heal.journalNameChem Biol Interacten
heal.journalTypepeer-reviewed-
heal.languageen-
heal.publicationDate1976-
heal.recordProviderΠανεπιστήμιο Ιωαννίνων. Σχολή Επιστημών Υγείας. Τμήμα Ιατρικήςel
heal.typejournalArticle-
heal.type.elΆρθρο Περιοδικούel
heal.type.enJournal articleen

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