Ransy 2020 Int J Mol Sci: Difference between revisions

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{{Publication
{{Publication
|title=Ransy C, Vaz C, Lombรจs A, Bouillaud F (2020) Use of H2O2 to cause oxidative stress, the catalase issue. Int J Mol Sci 21:9149. https://doi.org/10.3390/ijms21239149
|title=Ransy C, Vaz C, Lombรจs A, Bouillaud F (2020) Use of H<sub>2</sub>O<sub>2</sub> to cause oxidative stress, the catalase issue. Int J Mol Sci 21:9149. https://doi.org/10.3390/ijms21239149
|info=[https://pubmed.ncbi.nlm.nih.gov/33266350/ PMID: 33266350 Open Access]
|info=[https://pubmed.ncbi.nlm.nih.gov/33266350/ PMID: 33266350 Open Access]
|authors=Ransy C, Vaz C, Lombรจs A, Bouillaud F
|authors=Ransy C, Vaz C, Lombรจs A, Bouillaud F
|year=2020
|year=2020
|journal=Int J Mol Sci
|journal=Int J Mol Sci
|abstract=Addition of hydrogen peroxide (H2O2) 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 H2O2 addition results in O2 release as expected from catalase reaction. This reaction is fast enough to, within seconds, decrease drastically H2O2 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 (H2O2) defense. Thirdly, it complicates the interpretation of experiments as subsequent observations might result from high/transient H2O2 exposure and/or from the diverse possible consequences of the O2 release.
|abstract=Addition of hydrogen peroxide (H<sub>2</sub>O<sub>2</sub>) 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<sub>2</sub>O<sub>2</sub> addition results in O<sub>2</sub> release as expected from catalase reaction. This reaction is fast enough to, within seconds, decrease drastically H<sub>2</sub>O<sub>2</sub> 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<sub>2</sub>O<sub>2</sub>) defense. Thirdly, it complicates the interpretation of experiments as subsequent observations might result from high/transient H2O2 exposure and/or from the diverse possible consequences of the O<sub>2</sub> release.
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|editor=Gnaiger E
|editor=Gnaiger E
|mipnetlab=FR Paris Bouillaud F
|mipnetlab=FR Paris Bouillaud F
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|couplingstates=ROUTINE
|couplingstates=ROUTINE
|instruments=Oxygraph-2k
|instruments=Oxygraph-2k
|additional=Catalase
}}
}}

Latest revision as of 10:13, 7 March 2024

Publications in the MiPMap
Ransy C, Vaz C, Lombรจs A, Bouillaud F (2020) Use of H2O2 to cause oxidative stress, the catalase issue. Int J Mol Sci 21:9149. https://doi.org/10.3390/ijms21239149

ยป PMID: 33266350 Open Access

Ransy C, Vaz C, Lombรจs A, Bouillaud F (2020) Int J Mol Sci

Abstract: Addition of hydrogen peroxide (H2O2) 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 H2O2 addition results in O2 release as expected from catalase reaction. This reaction is fast enough to, within seconds, decrease drastically H2O2 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 (H2O2) defense. Thirdly, it complicates the interpretation of experiments as subsequent observations might result from high/transient H2O2 exposure and/or from the diverse possible consequences of the O2 release.

โ€ข Bioblast editor: Gnaiger E โ€ข O2k-Network Lab: FR Paris Bouillaud F


Labels: MiParea: Respiration 

Stress:Oxidative stress;RONS 

Tissue;cell: CHO  Preparation: Permeabilized cells, Intact cells 


Coupling state: ROUTINE 

HRR: Oxygraph-2k 

Catalase 

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