Hepatic enzymatic metabolism alterations and oxidative stress during the onset of carcinogenesis: Protective role of α-tocopherol

Oxidants play a role in several stages of carcinogenesis. A high antioxidant capacity is expected to protect 'initiated' cells from excessive oxidant toxicity. The aim of this study was to determine the chemopreventive effect of α-tocopherol (α-T) on the hepatocarcinogenesis induced with p...

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Autores principales: Gerez, Esther Noemí, Vázquez, Elba Susana, Batlle, Alcira María del Carmen
Publicado: 1998
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Acceso en línea:https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_09598278_v7_n1_p69_Gerez
http://hdl.handle.net/20.500.12110/paper_09598278_v7_n1_p69_Gerez
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spelling paper:paper_09598278_v7_n1_p69_Gerez2023-06-08T15:57:12Z Hepatic enzymatic metabolism alterations and oxidative stress during the onset of carcinogenesis: Protective role of α-tocopherol Gerez, Esther Noemí Vázquez, Elba Susana Batlle, Alcira María del Carmen α-Tocopherol Drug metabolizing enzyme system Heme metabolism Hepatocarcinogenesis Oxidative stress p-dimethylaminoazobenzene 4 dimethylaminoazobenzene 5 aminolevulinate synthase alpha tocopherol antioxidant cytochrome p450 glutathione transferase heme animal experiment animal model animal tissue antioxidant activity article controlled study liver cancer liver carcinogenesis liver metabolism male mouse nonhuman oxidative stress priority journal vitamin metabolism xenobiotic metabolism 5-Aminolevulinate Synthetase Animals Antioxidants Carcinogens Enzyme Induction Glutathione Transferase Liver Neoplasms, Experimental Male Mice Oxidative Stress p-Dimethylaminoazobenzene Vitamin E Oxidants play a role in several stages of carcinogenesis. A high antioxidant capacity is expected to protect 'initiated' cells from excessive oxidant toxicity. The aim of this study was to determine the chemopreventive effect of α-tocopherol (α-T) on the hepatocarcinogenesis induced with p- dimethylaminoazobenzene (DAB) in mice. The dietary administration of α-T completely reversed the induction of δ-aminolevulinate synthetase and glutathione-S-transferase (the tumoral marker enzyme). α-T greatly enhanced P 450 levels, which were even higher in animals exposed to DAB. Indirect evidence for the involvement of oxygen radicals in the DAB model of hepatocarcinogenesis was provided by increased levels of thiobarbituric acid reactive species, which were detected in animals with severe liver damage and were assessed by histological analysis. α-T reduced the degree of hepatic injury, although this vitamin produced only slight changes in the oxidative parameters evaluated. The use of α-T as a potential chemopreventive agent, particularly during the initiation stage of carcinogenesis provoked by DAB, is worthy of further study. 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:Del C. Batlle, A.M. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. 1998 https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_09598278_v7_n1_p69_Gerez http://hdl.handle.net/20.500.12110/paper_09598278_v7_n1_p69_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 α-Tocopherol
Drug metabolizing enzyme system
Heme metabolism
Hepatocarcinogenesis
Oxidative stress
p-dimethylaminoazobenzene
4 dimethylaminoazobenzene
5 aminolevulinate synthase
alpha tocopherol
antioxidant
cytochrome p450
glutathione transferase
heme
animal experiment
animal model
animal tissue
antioxidant activity
article
controlled study
liver cancer
liver carcinogenesis
liver metabolism
male
mouse
nonhuman
oxidative stress
priority journal
vitamin metabolism
xenobiotic metabolism
5-Aminolevulinate Synthetase
Animals
Antioxidants
Carcinogens
Enzyme Induction
Glutathione Transferase
Liver Neoplasms, Experimental
Male
Mice
Oxidative Stress
p-Dimethylaminoazobenzene
Vitamin E
spellingShingle α-Tocopherol
Drug metabolizing enzyme system
Heme metabolism
Hepatocarcinogenesis
Oxidative stress
p-dimethylaminoazobenzene
4 dimethylaminoazobenzene
5 aminolevulinate synthase
alpha tocopherol
antioxidant
cytochrome p450
glutathione transferase
heme
animal experiment
animal model
animal tissue
antioxidant activity
article
controlled study
liver cancer
liver carcinogenesis
liver metabolism
male
mouse
nonhuman
oxidative stress
priority journal
vitamin metabolism
xenobiotic metabolism
5-Aminolevulinate Synthetase
Animals
Antioxidants
Carcinogens
Enzyme Induction
Glutathione Transferase
Liver Neoplasms, Experimental
Male
Mice
Oxidative Stress
p-Dimethylaminoazobenzene
Vitamin E
Gerez, Esther Noemí
Vázquez, Elba Susana
Batlle, Alcira María del Carmen
Hepatic enzymatic metabolism alterations and oxidative stress during the onset of carcinogenesis: Protective role of α-tocopherol
topic_facet α-Tocopherol
Drug metabolizing enzyme system
Heme metabolism
Hepatocarcinogenesis
Oxidative stress
p-dimethylaminoazobenzene
4 dimethylaminoazobenzene
5 aminolevulinate synthase
alpha tocopherol
antioxidant
cytochrome p450
glutathione transferase
heme
animal experiment
animal model
animal tissue
antioxidant activity
article
controlled study
liver cancer
liver carcinogenesis
liver metabolism
male
mouse
nonhuman
oxidative stress
priority journal
vitamin metabolism
xenobiotic metabolism
5-Aminolevulinate Synthetase
Animals
Antioxidants
Carcinogens
Enzyme Induction
Glutathione Transferase
Liver Neoplasms, Experimental
Male
Mice
Oxidative Stress
p-Dimethylaminoazobenzene
Vitamin E
description Oxidants play a role in several stages of carcinogenesis. A high antioxidant capacity is expected to protect 'initiated' cells from excessive oxidant toxicity. The aim of this study was to determine the chemopreventive effect of α-tocopherol (α-T) on the hepatocarcinogenesis induced with p- dimethylaminoazobenzene (DAB) in mice. The dietary administration of α-T completely reversed the induction of δ-aminolevulinate synthetase and glutathione-S-transferase (the tumoral marker enzyme). α-T greatly enhanced P 450 levels, which were even higher in animals exposed to DAB. Indirect evidence for the involvement of oxygen radicals in the DAB model of hepatocarcinogenesis was provided by increased levels of thiobarbituric acid reactive species, which were detected in animals with severe liver damage and were assessed by histological analysis. α-T reduced the degree of hepatic injury, although this vitamin produced only slight changes in the oxidative parameters evaluated. The use of α-T as a potential chemopreventive agent, particularly during the initiation stage of carcinogenesis provoked by DAB, is worthy of further study.
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 Hepatic enzymatic metabolism alterations and oxidative stress during the onset of carcinogenesis: Protective role of α-tocopherol
title_short Hepatic enzymatic metabolism alterations and oxidative stress during the onset of carcinogenesis: Protective role of α-tocopherol
title_full Hepatic enzymatic metabolism alterations and oxidative stress during the onset of carcinogenesis: Protective role of α-tocopherol
title_fullStr Hepatic enzymatic metabolism alterations and oxidative stress during the onset of carcinogenesis: Protective role of α-tocopherol
title_full_unstemmed Hepatic enzymatic metabolism alterations and oxidative stress during the onset of carcinogenesis: Protective role of α-tocopherol
title_sort hepatic enzymatic metabolism alterations and oxidative stress during the onset of carcinogenesis: protective role of α-tocopherol
publishDate 1998
url https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_09598278_v7_n1_p69_Gerez
http://hdl.handle.net/20.500.12110/paper_09598278_v7_n1_p69_Gerez
work_keys_str_mv AT gerezesthernoemi hepaticenzymaticmetabolismalterationsandoxidativestressduringtheonsetofcarcinogenesisprotectiveroleofatocopherol
AT vazquezelbasusana hepaticenzymaticmetabolismalterationsandoxidativestressduringtheonsetofcarcinogenesisprotectiveroleofatocopherol
AT batllealciramariadelcarmen hepaticenzymaticmetabolismalterationsandoxidativestressduringtheonsetofcarcinogenesisprotectiveroleofatocopherol
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