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. 2021 Nov 12;12:755782. doi: 10.3389/fimmu.2021.755782

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Copyright © 2021 Teixeira, Ducret, Langen, Nogoceke, Santos, Silva Nunes, Benvenuti, Levy, Bydlowski, Bocchi, Kuramoto Takara, Fiorelli, Stolf, Pomeranzeff, Chevillard, Kalil and Cunha-Neto

This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

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Analysis of antioxidant enzyme Catalase and lipid peroxidation status. (A) Catalase protein levels measured by immunoblotting; the densitometric values were normalized by the total protein for each sample (One-Way ANOVA p = 0.0008). (B) Malondialdehyde (MDA) production, measured by the thiobarbituric acid reactive substances (TBARS) assay (One-Way ANOVA p = 0.0113). The horizontal lines show statistically significant changes between groups by the Tukey-Kramer test: **p < 0.01; ***p < 0.001.