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Combined Effect of AMPK/PPAR Agonists and Exercise Training in mdx Mice Functional Performance

The present investigation was undertaken to test whether exercise training (ET) associated with AMPK/PPAR agonists (EM) would improve skeletal muscle function in mdx mice. These drugs have the potential to improve oxidative metabolism. This is of particular interest because oxidative muscle fibers a...

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Autores principales: Bueno Júnior, Carlos R., Pantaleão, Lucas C., Voltarelli, Vanessa A., Bozi, Luiz Henrique M., Brum, Patricia Chakur, Zatz, Mayana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3448675/
https://www.ncbi.nlm.nih.gov/pubmed/23029189
http://dx.doi.org/10.1371/journal.pone.0045699
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author Bueno Júnior, Carlos R.
Pantaleão, Lucas C.
Voltarelli, Vanessa A.
Bozi, Luiz Henrique M.
Brum, Patricia Chakur
Zatz, Mayana
author_facet Bueno Júnior, Carlos R.
Pantaleão, Lucas C.
Voltarelli, Vanessa A.
Bozi, Luiz Henrique M.
Brum, Patricia Chakur
Zatz, Mayana
author_sort Bueno Júnior, Carlos R.
collection PubMed
description The present investigation was undertaken to test whether exercise training (ET) associated with AMPK/PPAR agonists (EM) would improve skeletal muscle function in mdx mice. These drugs have the potential to improve oxidative metabolism. This is of particular interest because oxidative muscle fibers are less affected in the course of the disease than glycolitic counterparts. Therefore, a cohort of 34 male congenic C57Bl/10J mdx mice included in this study was randomly assigned into four groups: vehicle solution (V), EM [AICAR (AMPK agonist, 50 mg/Kg-1.day-1, ip) and GW 1516 (PPARδ agonist, 2.5 mg/Kg-1.day-1, gavage)], ET (voluntary running on activity wheel) and EM+ET. Functional performance (grip meter and rotarod), aerobic capacity (running test), muscle histopathology, serum creatine kinase (CK), levels of ubiquitined proteins, oxidative metabolism protein expression (AMPK, PPAR, myoglobin and SCD) and intracellular calcium handling (DHPR, SERCA and NCX) protein expression were analyzed. Treatments started when the animals were two months old and were maintained for one month. A significant functional improvement (p<0.05) was observed in animals submitted to the combination of ET and EM. CK levels were decreased and the expression of proteins related to oxidative metabolism was increased in this group. There were no differences among the groups in the intracellular calcium handling protein expression. To our knowledge, this is the first study that tested the association of ET with EM in an experimental model of muscular dystrophy. Our results suggest that the association of ET and EM should be further tested as a potential therapeutic approach in muscular dystrophies.
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spelling pubmed-34486752012-10-01 Combined Effect of AMPK/PPAR Agonists and Exercise Training in mdx Mice Functional Performance Bueno Júnior, Carlos R. Pantaleão, Lucas C. Voltarelli, Vanessa A. Bozi, Luiz Henrique M. Brum, Patricia Chakur Zatz, Mayana PLoS One Research Article The present investigation was undertaken to test whether exercise training (ET) associated with AMPK/PPAR agonists (EM) would improve skeletal muscle function in mdx mice. These drugs have the potential to improve oxidative metabolism. This is of particular interest because oxidative muscle fibers are less affected in the course of the disease than glycolitic counterparts. Therefore, a cohort of 34 male congenic C57Bl/10J mdx mice included in this study was randomly assigned into four groups: vehicle solution (V), EM [AICAR (AMPK agonist, 50 mg/Kg-1.day-1, ip) and GW 1516 (PPARδ agonist, 2.5 mg/Kg-1.day-1, gavage)], ET (voluntary running on activity wheel) and EM+ET. Functional performance (grip meter and rotarod), aerobic capacity (running test), muscle histopathology, serum creatine kinase (CK), levels of ubiquitined proteins, oxidative metabolism protein expression (AMPK, PPAR, myoglobin and SCD) and intracellular calcium handling (DHPR, SERCA and NCX) protein expression were analyzed. Treatments started when the animals were two months old and were maintained for one month. A significant functional improvement (p<0.05) was observed in animals submitted to the combination of ET and EM. CK levels were decreased and the expression of proteins related to oxidative metabolism was increased in this group. There were no differences among the groups in the intracellular calcium handling protein expression. To our knowledge, this is the first study that tested the association of ET with EM in an experimental model of muscular dystrophy. Our results suggest that the association of ET and EM should be further tested as a potential therapeutic approach in muscular dystrophies. Public Library of Science 2012-09-21 /pmc/articles/PMC3448675/ /pubmed/23029189 http://dx.doi.org/10.1371/journal.pone.0045699 Text en © 2012 Bueno Júnior et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Bueno Júnior, Carlos R.
Pantaleão, Lucas C.
Voltarelli, Vanessa A.
Bozi, Luiz Henrique M.
Brum, Patricia Chakur
Zatz, Mayana
Combined Effect of AMPK/PPAR Agonists and Exercise Training in mdx Mice Functional Performance
title Combined Effect of AMPK/PPAR Agonists and Exercise Training in mdx Mice Functional Performance
title_full Combined Effect of AMPK/PPAR Agonists and Exercise Training in mdx Mice Functional Performance
title_fullStr Combined Effect of AMPK/PPAR Agonists and Exercise Training in mdx Mice Functional Performance
title_full_unstemmed Combined Effect of AMPK/PPAR Agonists and Exercise Training in mdx Mice Functional Performance
title_short Combined Effect of AMPK/PPAR Agonists and Exercise Training in mdx Mice Functional Performance
title_sort combined effect of ampk/ppar agonists and exercise training in mdx mice functional performance
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3448675/
https://www.ncbi.nlm.nih.gov/pubmed/23029189
http://dx.doi.org/10.1371/journal.pone.0045699
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