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Título: | Response of the antioxidant defense system to tert-butyl hydroperoxide and hydrogen peroxide in a human hepatoma cell line (HepG2) |
Autor: | Alía, Mario; Ramos, Sonia CSIC ORCID ; Mateos, Raquel CSIC ORCID ; Bravo, Laura CSIC ORCID; Goya, Luis CSIC ORCID | Palabras clave: | Malondialdehyde Antioxidant enzymes Reduced Glutathione Reactive Oxygen Species Cytotoxicity Human Hepatoma Cells Pro-Oxidants |
Fecha de publicación: | 2005 | Editor: | Wiley-Blackwell | Citación: | Journal of Biochemical and Molecular Toxicology 19(2): 119-128 (2005) | Resumen: | The aim of this work was to investigate the response of the antioxidant defense system to two oxidative stressors, hydrogen peroxide and tert-butyl hydroperoxide, in HepG2 cells in culture. The parameters evaluated included enzyme activity and gene expression of superoxide dismutase, catalase, glutathione peroxidase, and activity of glutathione reductase. Besides, markers of the cell damage and oxidative stress evoked by the stressors such as cell viability, intracellular reactive oxygen species generation, malondialdehyde levels, and reduced glutathione concentration were evaluated. Both stressors, hydrogen peroxide and tert-butyl hydroperoxide, enhanced cell damage and reactive oxygen species generation at doses above 50 μM. The concentration of reduced glutathione decreased, and levels of malondialdehyde and activity of the antioxidant enzymes consistently increased only when HepG2 cells were treated with tert-butyl hydroperoxide but not when hydrogen peroxide was used. A slight increase in the gene expression of Cu/Zn superoxide dismutase and catalase with 500 μM tert-butyl hydroperoxide and of catalase with 200 μM hydrogen peroxide was observed. The response of the components of the antioxidant defense system evaluated in this study indicates that tert-butyl hydroperoxide evokes a consistent cellular stress in HepG2. © 2005 Wiley Periodicals, Inc. | URI: | http://hdl.handle.net/10261/88618 | DOI: | 10.1002/jbt.20061 | Identificadores: | doi: 10.1002/jbt.20061 issn: 1095-6670 |
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