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Use of H(2)O(2) to Cause Oxidative Stress, the Catalase Issue

Addition of hydrogen peroxide (H(2)O(2)) is a method commonly used to trigger cellular oxidative stress. However, the doses used (often hundreds of micromolar) are disproportionally high with regard to physiological oxygen concentration (low micromolar). In this study using polarographic measurement...

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Detalles Bibliográficos
Autores principales: Ransy, Céline, Vaz, Clément, Lombès, Anne, Bouillaud, Frédéric
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7731207/
https://www.ncbi.nlm.nih.gov/pubmed/33266350
http://dx.doi.org/10.3390/ijms21239149
Descripción
Sumario:Addition of hydrogen peroxide (H(2)O(2)) is a method commonly used to trigger cellular oxidative stress. However, the doses used (often hundreds of micromolar) are disproportionally high with regard to physiological oxygen concentration (low micromolar). In this study using polarographic measurement of oxygen concentration in cellular suspensions we show that H(2)O(2) addition results in O(2) release as expected from catalase reaction. This reaction is fast enough to, within seconds, decrease drastically H(2)O(2) concentration and to annihilate it within a few minutes. Firstly, this is likely to explain why recording of oxidative damage requires the high concentrations found in the literature. Secondly, it illustrates the potency of intracellular antioxidant (H(2)O(2)) defense. Thirdly, it complicates the interpretation of experiments as subsequent observations might result from high/transient H(2)O(2) exposure and/or from the diverse possible consequences of the O(2) release.