Oxidative Stress, Inflammation, and Activators of Mitochondrial Biogenesis: Tempol Targets in the Diaphragm Muscle of Exercise Trained-mdx Mice

The mdx mouse phenotype aggravated by chronic exercise on a treadmill makes this murine model more reliable for the study of muscular dystrophy. Thus, to better assess the Tempol effect on dystrophic pathways, the analyses in this study were performed in the blood samples and diaphragm muscle from t...

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Main Authors: Heloina Nathalliê Mariano da Silva, Caroline Covatti, Guilherme Luiz da Rocha, Daniela Sayuri Mizobuti, Rafael Dias Mâncio, Túlio de Almeida Hermes, Larissa Akemi Kido, Valéria Helena Alves Cagnon, Elaine Cristina Leite Pereira, Elaine Minatel
Format: Article
Language:English
Published: Frontiers Media S.A. 2021-04-01
Series:Frontiers in Physiology
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fphys.2021.649793/full
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author Heloina Nathalliê Mariano da Silva
Caroline Covatti
Guilherme Luiz da Rocha
Daniela Sayuri Mizobuti
Rafael Dias Mâncio
Túlio de Almeida Hermes
Larissa Akemi Kido
Valéria Helena Alves Cagnon
Elaine Cristina Leite Pereira
Elaine Cristina Leite Pereira
Elaine Minatel
author_facet Heloina Nathalliê Mariano da Silva
Caroline Covatti
Guilherme Luiz da Rocha
Daniela Sayuri Mizobuti
Rafael Dias Mâncio
Túlio de Almeida Hermes
Larissa Akemi Kido
Valéria Helena Alves Cagnon
Elaine Cristina Leite Pereira
Elaine Cristina Leite Pereira
Elaine Minatel
author_sort Heloina Nathalliê Mariano da Silva
collection DOAJ
description The mdx mouse phenotype aggravated by chronic exercise on a treadmill makes this murine model more reliable for the study of muscular dystrophy. Thus, to better assess the Tempol effect on dystrophic pathways, the analyses in this study were performed in the blood samples and diaphragm muscle from treadmill trained adult (7–11-weeks old) mdx animals. The mdx mice were divided into three groups: mdxSed, sedentary controls (n = 28); mdxEx, exercise-trained animals (n = 28); and mdxEx+T, exercise-trained animals with the Tempol treatment (n = 28). The results demonstrated that the Tempol treatment promoted muscle strength gain, prevented muscle damage, reduced the inflammatory process, oxidative stress, and angiogenesis regulator, and up regulated the activators of mitochondrial biogenesis. The main new findings of this study are that Tempol reduced the NF-κB and increased the PGC1-α and PPARδ levels in the exercise-trained-mdx mice, which are probably related to the ability of this antioxidant to scavenge excessive ROS. These results reinforce the use of Tempol as a potential therapeutic strategy in DMD.
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spelling doaj.art-5ed0933327f44dffa343afe6ec9bc76a2022-12-21T18:53:59ZengFrontiers Media S.A.Frontiers in Physiology1664-042X2021-04-011210.3389/fphys.2021.649793649793Oxidative Stress, Inflammation, and Activators of Mitochondrial Biogenesis: Tempol Targets in the Diaphragm Muscle of Exercise Trained-mdx MiceHeloina Nathalliê Mariano da Silva0Caroline Covatti1Guilherme Luiz da Rocha2Daniela Sayuri Mizobuti3Rafael Dias Mâncio4Túlio de Almeida Hermes5Larissa Akemi Kido6Valéria Helena Alves Cagnon7Elaine Cristina Leite Pereira8Elaine Cristina Leite Pereira9Elaine Minatel10Department of Structural and Functional Biology, Institute of Biology, State University of Campinas (UNICAMP), Campinas, BrazilDepartment of Structural and Functional Biology, Institute of Biology, State University of Campinas (UNICAMP), Campinas, BrazilDepartment of Structural and Functional Biology, Institute of Biology, State University of Campinas (UNICAMP), Campinas, BrazilDepartment of Structural and Functional Biology, Institute of Biology, State University of Campinas (UNICAMP), Campinas, BrazilDepartment of Structural and Functional Biology, Institute of Biology, State University of Campinas (UNICAMP), Campinas, BrazilDepartment of Structural and Functional Biology, Institute of Biology, State University of Campinas (UNICAMP), Campinas, BrazilDepartment of Structural and Functional Biology, Institute of Biology, State University of Campinas (UNICAMP), Campinas, BrazilDepartment of Structural and Functional Biology, Institute of Biology, State University of Campinas (UNICAMP), Campinas, BrazilDepartment of Structural and Functional Biology, Institute of Biology, State University of Campinas (UNICAMP), Campinas, BrazilFaculty of Ceilândia, University of Brasília (UnB), Brasília, BrazilDepartment of Structural and Functional Biology, Institute of Biology, State University of Campinas (UNICAMP), Campinas, BrazilThe mdx mouse phenotype aggravated by chronic exercise on a treadmill makes this murine model more reliable for the study of muscular dystrophy. Thus, to better assess the Tempol effect on dystrophic pathways, the analyses in this study were performed in the blood samples and diaphragm muscle from treadmill trained adult (7–11-weeks old) mdx animals. The mdx mice were divided into three groups: mdxSed, sedentary controls (n = 28); mdxEx, exercise-trained animals (n = 28); and mdxEx+T, exercise-trained animals with the Tempol treatment (n = 28). The results demonstrated that the Tempol treatment promoted muscle strength gain, prevented muscle damage, reduced the inflammatory process, oxidative stress, and angiogenesis regulator, and up regulated the activators of mitochondrial biogenesis. The main new findings of this study are that Tempol reduced the NF-κB and increased the PGC1-α and PPARδ levels in the exercise-trained-mdx mice, which are probably related to the ability of this antioxidant to scavenge excessive ROS. These results reinforce the use of Tempol as a potential therapeutic strategy in DMD.https://www.frontiersin.org/articles/10.3389/fphys.2021.649793/fulltempoldystrophic musclesexerciseoxidative stressinflammatory process
spellingShingle Heloina Nathalliê Mariano da Silva
Caroline Covatti
Guilherme Luiz da Rocha
Daniela Sayuri Mizobuti
Rafael Dias Mâncio
Túlio de Almeida Hermes
Larissa Akemi Kido
Valéria Helena Alves Cagnon
Elaine Cristina Leite Pereira
Elaine Cristina Leite Pereira
Elaine Minatel
Oxidative Stress, Inflammation, and Activators of Mitochondrial Biogenesis: Tempol Targets in the Diaphragm Muscle of Exercise Trained-mdx Mice
Frontiers in Physiology
tempol
dystrophic muscles
exercise
oxidative stress
inflammatory process
title Oxidative Stress, Inflammation, and Activators of Mitochondrial Biogenesis: Tempol Targets in the Diaphragm Muscle of Exercise Trained-mdx Mice
title_full Oxidative Stress, Inflammation, and Activators of Mitochondrial Biogenesis: Tempol Targets in the Diaphragm Muscle of Exercise Trained-mdx Mice
title_fullStr Oxidative Stress, Inflammation, and Activators of Mitochondrial Biogenesis: Tempol Targets in the Diaphragm Muscle of Exercise Trained-mdx Mice
title_full_unstemmed Oxidative Stress, Inflammation, and Activators of Mitochondrial Biogenesis: Tempol Targets in the Diaphragm Muscle of Exercise Trained-mdx Mice
title_short Oxidative Stress, Inflammation, and Activators of Mitochondrial Biogenesis: Tempol Targets in the Diaphragm Muscle of Exercise Trained-mdx Mice
title_sort oxidative stress inflammation and activators of mitochondrial biogenesis tempol targets in the diaphragm muscle of exercise trained mdx mice
topic tempol
dystrophic muscles
exercise
oxidative stress
inflammatory process
url https://www.frontiersin.org/articles/10.3389/fphys.2021.649793/full
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