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dc.contributor.authorSURMEN, E
dc.contributor.authorERYUREK, FG
dc.date.accessioned2021-03-03T15:01:41Z
dc.date.available2021-03-03T15:01:41Z
dc.date.issued1992
dc.identifier.citationSURMEN E., ERYUREK F., "LIVER DELTA-AMINOLEVULINATE DEHYDRATASE ACTIVITY IN AMITRIPTYLINE-TREATED OR CHLORPROMAZINE-TREATED RATS", TOXICOLOGY, cilt.75, sa.1, ss.63-69, 1992
dc.identifier.issn0300-483X
dc.identifier.otherav_3cca08ce-5ab0-4eaa-8eec-8b0e4fc869f6
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/44776
dc.identifier.urihttps://doi.org/10.1016/0300-483x(92)90126-y
dc.description.abstractAmitriptyline (AMT) and chlorpromazine (CPZ) (0.5 mg per animal, i.p.) were injected into rats separately for 30 days and their effects on heme metabolism in liver were examined. Significant decreases in the delta-aminolevulinate dehydratase activity were observed following the administration of both drugs (mean value of AMT-group: 6.58 U/g tissue; and CPZ-group: 7.04 U/g tissue) in comparison to that of controls (11.71 U/g tissue); however total liver heme content was not altered. When 24-h urinary excretions of delta-aminolevulinate (ALA) and porphobilinogen (PBG) were measured on the last day of the experiment, a slight (AMT-group: 38.40 mug/day) to distinct (CPZ-group: 59.11 mug/day) increase of urinary ALA was observed, while PBG excretion tended to decline only moderately under CPZ (3.52 mug/day), but significantly in presence of AMT (2.16 mug/day). Mean values obtained from control group were 32.12 mug/day for ALA and 4.25 mug/day for PBG.
dc.language.isoeng
dc.subjectFarmasötik Toksikoloji
dc.subjectYaşam Bilimleri
dc.subjectTemel Bilimler
dc.subjectEczacılık
dc.subjectMeslek Bilimleri
dc.subjectTemel Eczacılık Bilimleri
dc.subjectSağlık Bilimleri
dc.subjectTOKSİKOLOJİ
dc.subjectYaşam Bilimleri (LIFE)
dc.subjectFarmakoloji ve Toksikoloji
dc.subjectFARMAKOLOJİ VE ECZACILIK
dc.titleLIVER DELTA-AMINOLEVULINATE DEHYDRATASE ACTIVITY IN AMITRIPTYLINE-TREATED OR CHLORPROMAZINE-TREATED RATS
dc.typeMakale
dc.relation.journalTOXICOLOGY
dc.contributor.department, ,
dc.identifier.volume75
dc.identifier.issue1
dc.identifier.startpage63
dc.identifier.endpage69
dc.contributor.firstauthorID113771


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