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spelling paper:paper_03063623_v29_n2_p207_Polo2023-06-08T15:31:08Z Griseofulvin-induced hepatopathy due to abnormalities in heme pathways Buzaleh, Ana María Vázquez, Elba Susana Afonso, Susana Graciela Batlle, Alcira María del Carmen Cholestasis Griseofulvan Heme pathway Hepatopathy alkaline phosphatase aspartate aminotransferase bilirubin bilirubin glucuronide griseofulvin heme porphyrin xenobiotic agent animal experiment animal tissue article cholestasis controlled study liver disease liver injury liver level long term exposure male microscopy mouse nonhuman priority journal topical drug administration Administration, Topical Animals Antibiotics, Antifungal Biological Markers Griseofulvin Heme Liver Liver Function Tests Male Mice 1. The effect of long term griseofulvin (GRIS) topical administration on some indica tors of liver damage was examined. 2. Liver porphyrin accumulation was significant; however, no porphyrin crystals were observed under light microscopy, 3. An earlier onset of hepatopathy was established (3-fold) increase of direct bilirubin values after 7 days of treatment; hepatic injury was confirmed by measuring a g fold increase of free bilirubin. 4. Enhanced values of alkaline phosphatase and glutamic oxalacetic transaminase (GOT) confirmed the onset of cholestasis. 5. Topical application of GRIS induced measurable hepatopathy. Nevertheless, we cannot discard the possibility that this hepatopathy could also be attributed in part to a direct reaction to xenobiotics. Fil:Buzaleh, A.M. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Vazquez, E.S. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Afonso, S.G. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Del Carmen Batlle, A.M. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. 1997 https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_03063623_v29_n2_p207_Polo http://hdl.handle.net/20.500.12110/paper_03063623_v29_n2_p207_Polo
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic Cholestasis
Griseofulvan
Heme pathway
Hepatopathy
alkaline phosphatase
aspartate aminotransferase
bilirubin
bilirubin glucuronide
griseofulvin
heme
porphyrin
xenobiotic agent
animal experiment
animal tissue
article
cholestasis
controlled study
liver disease
liver injury
liver level
long term exposure
male
microscopy
mouse
nonhuman
priority journal
topical drug administration
Administration, Topical
Animals
Antibiotics, Antifungal
Biological Markers
Griseofulvin
Heme
Liver
Liver Function Tests
Male
Mice
spellingShingle Cholestasis
Griseofulvan
Heme pathway
Hepatopathy
alkaline phosphatase
aspartate aminotransferase
bilirubin
bilirubin glucuronide
griseofulvin
heme
porphyrin
xenobiotic agent
animal experiment
animal tissue
article
cholestasis
controlled study
liver disease
liver injury
liver level
long term exposure
male
microscopy
mouse
nonhuman
priority journal
topical drug administration
Administration, Topical
Animals
Antibiotics, Antifungal
Biological Markers
Griseofulvin
Heme
Liver
Liver Function Tests
Male
Mice
Buzaleh, Ana María
Vázquez, Elba Susana
Afonso, Susana Graciela
Batlle, Alcira María del Carmen
Griseofulvin-induced hepatopathy due to abnormalities in heme pathways
topic_facet Cholestasis
Griseofulvan
Heme pathway
Hepatopathy
alkaline phosphatase
aspartate aminotransferase
bilirubin
bilirubin glucuronide
griseofulvin
heme
porphyrin
xenobiotic agent
animal experiment
animal tissue
article
cholestasis
controlled study
liver disease
liver injury
liver level
long term exposure
male
microscopy
mouse
nonhuman
priority journal
topical drug administration
Administration, Topical
Animals
Antibiotics, Antifungal
Biological Markers
Griseofulvin
Heme
Liver
Liver Function Tests
Male
Mice
description 1. The effect of long term griseofulvin (GRIS) topical administration on some indica tors of liver damage was examined. 2. Liver porphyrin accumulation was significant; however, no porphyrin crystals were observed under light microscopy, 3. An earlier onset of hepatopathy was established (3-fold) increase of direct bilirubin values after 7 days of treatment; hepatic injury was confirmed by measuring a g fold increase of free bilirubin. 4. Enhanced values of alkaline phosphatase and glutamic oxalacetic transaminase (GOT) confirmed the onset of cholestasis. 5. Topical application of GRIS induced measurable hepatopathy. Nevertheless, we cannot discard the possibility that this hepatopathy could also be attributed in part to a direct reaction to xenobiotics.
author Buzaleh, Ana María
Vázquez, Elba Susana
Afonso, Susana Graciela
Batlle, Alcira María del Carmen
author_facet Buzaleh, Ana María
Vázquez, Elba Susana
Afonso, Susana Graciela
Batlle, Alcira María del Carmen
author_sort Buzaleh, Ana María
title Griseofulvin-induced hepatopathy due to abnormalities in heme pathways
title_short Griseofulvin-induced hepatopathy due to abnormalities in heme pathways
title_full Griseofulvin-induced hepatopathy due to abnormalities in heme pathways
title_fullStr Griseofulvin-induced hepatopathy due to abnormalities in heme pathways
title_full_unstemmed Griseofulvin-induced hepatopathy due to abnormalities in heme pathways
title_sort griseofulvin-induced hepatopathy due to abnormalities in heme pathways
publishDate 1997
url https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_03063623_v29_n2_p207_Polo
http://hdl.handle.net/20.500.12110/paper_03063623_v29_n2_p207_Polo
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AT afonsosusanagraciela griseofulvininducedhepatopathyduetoabnormalitiesinhemepathways
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