Altered heme pathway regulation and drug metabolizing enzyme system in a mouse model of hepatocarcinogenesis: Effect of veronal

1. Male CF 1 mice were fed p-dimethylaminoazobenzene (DAB) for 35 days and received 5,5 diethylbarbituric acid, before or after DAB treatment, with the purpose of investigating whether the onset of the preinitiation stage of carcinogenesis alters the natural regulatory mechanism of the heme pathway....

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Autores principales: Gerez, Esther Noemí, Vázquez, Elba Susana, Batlle, Alcira María del Carmen
Publicado: 1997
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Acceso en línea:https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_03063623_v29_n4_p569_Gerez
http://hdl.handle.net/20.500.12110/paper_03063623_v29_n4_p569_Gerez
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spelling paper:paper_03063623_v29_n4_p569_Gerez2023-06-08T15:31:08Z Altered heme pathway regulation and drug metabolizing enzyme system in a mouse model of hepatocarcinogenesis: Effect of veronal Gerez, Esther Noemí Vázquez, Elba Susana Batlle, Alcira María del Carmen Azo-dye Drug metabolizing enzyme system Heme metabolism Hepatocarcinogenesis Porphyrinogen drug 4 dimethylaminoazobenzene 5 aminolevulinate synthase barbital cytochrome p450 heme oxygenase animal model animal tissue article controlled study enzyme activity heme synthesis liver carcinogenesis male mouse nonhuman priority journal 1. Male CF 1 mice were fed p-dimethylaminoazobenzene (DAB) for 35 days and received 5,5 diethylbarbituric acid, before or after DAB treatment, with the purpose of investigating whether the onset of the preinitiation stage of carcinogenesis alters the natural regulatory mechanism of the heme pathway. 2. Changes detected in drug metabolizing enzymes are likely to be the consequence of a primary deregulation mechanism of heme metabolism, shown by an increase in 6 aminolevulinic acid synthetase activity and a decrease in microsomal heme oxygenase, which would finally lead to a great enhancement of cytochrome P450 levels. 3. The alterations found here would give rise to a pattern distinctive to that usually observed in the so called resistant hepatocyte. Fil:Gerez, E. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Vazquez, E. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Batlle, A. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. 1997 https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_03063623_v29_n4_p569_Gerez http://hdl.handle.net/20.500.12110/paper_03063623_v29_n4_p569_Gerez
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic Azo-dye
Drug metabolizing enzyme system
Heme metabolism
Hepatocarcinogenesis
Porphyrinogen drug
4 dimethylaminoazobenzene
5 aminolevulinate synthase
barbital
cytochrome p450
heme oxygenase
animal model
animal tissue
article
controlled study
enzyme activity
heme synthesis
liver carcinogenesis
male
mouse
nonhuman
priority journal
spellingShingle Azo-dye
Drug metabolizing enzyme system
Heme metabolism
Hepatocarcinogenesis
Porphyrinogen drug
4 dimethylaminoazobenzene
5 aminolevulinate synthase
barbital
cytochrome p450
heme oxygenase
animal model
animal tissue
article
controlled study
enzyme activity
heme synthesis
liver carcinogenesis
male
mouse
nonhuman
priority journal
Gerez, Esther Noemí
Vázquez, Elba Susana
Batlle, Alcira María del Carmen
Altered heme pathway regulation and drug metabolizing enzyme system in a mouse model of hepatocarcinogenesis: Effect of veronal
topic_facet Azo-dye
Drug metabolizing enzyme system
Heme metabolism
Hepatocarcinogenesis
Porphyrinogen drug
4 dimethylaminoazobenzene
5 aminolevulinate synthase
barbital
cytochrome p450
heme oxygenase
animal model
animal tissue
article
controlled study
enzyme activity
heme synthesis
liver carcinogenesis
male
mouse
nonhuman
priority journal
description 1. Male CF 1 mice were fed p-dimethylaminoazobenzene (DAB) for 35 days and received 5,5 diethylbarbituric acid, before or after DAB treatment, with the purpose of investigating whether the onset of the preinitiation stage of carcinogenesis alters the natural regulatory mechanism of the heme pathway. 2. Changes detected in drug metabolizing enzymes are likely to be the consequence of a primary deregulation mechanism of heme metabolism, shown by an increase in 6 aminolevulinic acid synthetase activity and a decrease in microsomal heme oxygenase, which would finally lead to a great enhancement of cytochrome P450 levels. 3. The alterations found here would give rise to a pattern distinctive to that usually observed in the so called resistant hepatocyte.
author Gerez, Esther Noemí
Vázquez, Elba Susana
Batlle, Alcira María del Carmen
author_facet Gerez, Esther Noemí
Vázquez, Elba Susana
Batlle, Alcira María del Carmen
author_sort Gerez, Esther Noemí
title Altered heme pathway regulation and drug metabolizing enzyme system in a mouse model of hepatocarcinogenesis: Effect of veronal
title_short Altered heme pathway regulation and drug metabolizing enzyme system in a mouse model of hepatocarcinogenesis: Effect of veronal
title_full Altered heme pathway regulation and drug metabolizing enzyme system in a mouse model of hepatocarcinogenesis: Effect of veronal
title_fullStr Altered heme pathway regulation and drug metabolizing enzyme system in a mouse model of hepatocarcinogenesis: Effect of veronal
title_full_unstemmed Altered heme pathway regulation and drug metabolizing enzyme system in a mouse model of hepatocarcinogenesis: Effect of veronal
title_sort altered heme pathway regulation and drug metabolizing enzyme system in a mouse model of hepatocarcinogenesis: effect of veronal
publishDate 1997
url https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_03063623_v29_n4_p569_Gerez
http://hdl.handle.net/20.500.12110/paper_03063623_v29_n4_p569_Gerez
work_keys_str_mv AT gerezesthernoemi alteredhemepathwayregulationanddrugmetabolizingenzymesysteminamousemodelofhepatocarcinogenesiseffectofveronal
AT vazquezelbasusana alteredhemepathwayregulationanddrugmetabolizingenzymesysteminamousemodelofhepatocarcinogenesiseffectofveronal
AT batllealciramariadelcarmen alteredhemepathwayregulationanddrugmetabolizingenzymesysteminamousemodelofhepatocarcinogenesiseffectofveronal
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