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

PLoS One. 2020 Aug 12;15(8):e0236689. doi: 10.1371/journal.pone.0236689. eCollection 2020.

Abstract

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<0.0001). In contrast, the use of NSAIDs did not appear to add benefits to skeletal muscle tissue in mdx mice.

Conclusion: We believe that the promising and optimistic results about the PBMT in skeletal muscle of mdx mice may in the future contribute to this therapy to be considered a safe alternative for patients with Duchenne Muscular Dystrophy (DMD) in a washout period (between treatment periods with glucocorticoids), allowing them to remain receiving effective and safe treatment in this period, avoiding at this way periods without administration of any treatment.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Anti-Inflammatory Agents, Non-Steroidal / pharmacology
  • Combined Modality Therapy
  • Disease Models, Animal
  • Disease Progression
  • Dystrophin / genetics*
  • Gene Expression Regulation / drug effects
  • Gene Expression Regulation / radiation effects
  • Glucocorticoids / pharmacology
  • Humans
  • Low-Level Light Therapy*
  • Mice
  • Mice, Inbred mdx
  • Muscle, Skeletal / drug effects*
  • Muscle, Skeletal / metabolism
  • Muscle, Skeletal / radiation effects*
  • Muscular Dystrophy, Duchenne / genetics
  • Muscular Dystrophy, Duchenne / metabolism
  • Muscular Dystrophy, Duchenne / physiopathology
  • Muscular Dystrophy, Duchenne / therapy*
  • Prednisone / pharmacology

Substances

  • Anti-Inflammatory Agents, Non-Steroidal
  • Dystrophin
  • Glucocorticoids
  • Prednisone

Grants and funding

This study was supported by research grants #310281/2017-2 and #429765/2018-5 from Brazilian Council of Science and Technology Development - CNPq (Professor Ernesto Cesar Pinto Leal-Junior), and #2015/21012-2, São Paulo Research Foundation (FAPESP) (Professor Lucio Frigo). The funders had no role in study design; data collection and analysis, decision to publish, or preparation of the manuscript.