Can photobiomodulation therapy be an alternative to pharmacological therapies in decreasing the progression of skeletal muscle impairments of mdx mice?

Objective To compare the effects of photobiomodulation therapy (PBMT) and pharmacological therapy (glucocorticoids and non-steroidal anti-inflammatory drugs) applied alone and in different combinations in mdx mice. Methods The animals were randomized and divided into seven experimental groups treate...

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Veröffentlicht in:PloS one 2020-08, Vol.15 (8), p.e0236689-e0236689
Hauptverfasser: Tomazoni, Shaiane Silva, Casalechi, Heliodora Leao, Ferreira, Cheila de Sousa Bacelar, Serra, Andrey Jorge, Dellê, Humberto, Brito, Rodrigo Barbosa de Oliveira, de Melo, Brunno Lemes, Vanin, Adriane Aver, Ribeiro, Neide Firmo, Pereira, Amanda Lima, Monteiro, Kadma Karenina Damasceno Soares, Marcos, Rodrigo Labat, de Carvalho, Paulo de Tarso Camillo, Frigo, Lucio, Leal-Junior, Ernesto Cesar Pinto
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Sprache:eng
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Zusammenfassung:Objective To compare the effects of photobiomodulation therapy (PBMT) and pharmacological therapy (glucocorticoids and non-steroidal anti-inflammatory drugs) applied alone and in different combinations in mdx mice. Methods The animals were randomized and divided into seven experimental groups treated with placebo, PBMT, prednisone, non-steroidal anti-inflammatory drug (NSAIDs), PBMT plus prednisone and PBMT plus NSAID. Wild type animals were used as control. All treatments were performed during 14 consecutive weeks. Muscular morphology, protein expression of dystrophin and functional performance were assessed at the end of the last treatment. Results Both treatments with prednisone and PBMT applied alone or combined, were effective in preserving muscular morphology. In addition, the treatments with PBMT (p = 0.0005), PBMT plus prednisone (p = 0.0048) and PBMT plus NSAID (p = 0.0021) increased dystrophin gene expression compared to placebo-control group. However, in the functional performance the PBMT presented better results compared to glucocorticoids (p
ISSN:1932-6203
1932-6203
DOI:10.1371/journal.pone.0236689