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Swimming Improves Memory and Antioxidant Defense in an Animal Model of Duchenne Muscular Dystrophy

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Abstract

Duchenne muscular dystrophy (DMD) is a genetic disease associated with progressive skeletal muscle degeneration. In humans, DMD has an early onset, causes developmental delays, and is a devastating disease that drastically diminishes the quality of life of young individuals affected. The objective of this study was to evaluate the effects of a swimming protocol on memory and oxidative stress in an animal model of DMD. Male mdx and wild-type mice aged ≥ 28 days were used in this study. The animals were trained for a stepped swimming protocol for four consecutive weeks. The swimming protocol significantly reduced the levels of lipid peroxidation and protein carbonylation in the gastrocnemius, hippocampus, and striatum in the exercised animals. It also prevented lipid peroxidation in the diaphragm. Moreover, it increased the free thiol levels in the gastrocnemius, the diaphragm, and all central nervous system structures. The results showed that the protocol that applied swimming as a low-intensity aerobic exercise for 4 weeks prevented aversive memory and habituation in mdx mice.

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Funding

This research was supported by grants from Unisul (CMC) and the UNIEDU/FUMDES (AA).

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Priscila Mantovani Nocetti, Viviane Freiberger, and Letícia Ventura planned the experiments and wrote the paper. Clarissa Martinelli Comim managed the project and performed most of the experiments and analysis and provided input on statistical analysis and interpretation. Adriano Alberti provided substantial input for the manuscript and wrote the paper. Daniel Fernandes Martins, Leoberto Ricardo Grigollo, Cristina Salar Andreau, and Rudy José Nodari Junior provided technical guidance and supervision. All authors read and approved the final manuscript.

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Correspondence to Adriano Alberti.

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Nocetti, P.M., Alberti, A., Freiberger, V. et al. Swimming Improves Memory and Antioxidant Defense in an Animal Model of Duchenne Muscular Dystrophy. Mol Neurobiol 58, 5067–5077 (2021). https://doi.org/10.1007/s12035-021-02482-y

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