Pre-exercise low-level laser therapy improves performance and levels of oxidative stress markers in mdx mice subjected to muscle fatigue by high-intensity exercise
This study was designed to determine if the levels of oxidative stress markers are influenced by low-level laser therapy (LLLT) in mdx mice subjected to high-intensity exercise training on an electric treadmill. We used 21 C57BL/10ScSn-Dmdmdx/J mice and 7 C57BL/10ScSn mice, all aged 4 weeks. The mic...
Gespeichert in:
Veröffentlicht in: | Lasers in medical science 2015-08, Vol.30 (6), p.1719-1727 |
---|---|
Hauptverfasser: | , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
Zusammenfassung: | This study was designed to determine if the levels of oxidative stress markers are influenced by low-level laser therapy (LLLT) in
mdx
mice subjected to high-intensity exercise training on an electric treadmill. We used 21 C57BL/10ScSn-Dmdmdx/J mice and 7 C57BL/10ScSn mice, all aged 4 weeks. The mice were divided into four groups: a positive control group of normal, wild-type mice (WT); a negative control group of untreated
mdx
mice; a group of
mdx
mice that underwent forced high-intensity exercise on a treadmill (
mdx
fatigue); and another group of
mdx
mice with the same characteristics that were treated with LLLT at a single point on the gastrocnemius muscle of the hind paw and underwent forced high-intensity exercise on a treadmill. The
mdx
mice treated with LLLT showed significantly lower levels of creatine kinase (CK) and oxidative stress than
mdx
mice that underwent forced high-intensity exercise on a treadmill. The activities of the antioxidant enzyme superoxide dismutase (SOD) were higher in control
mdx
mice than in WT mice. LLLT also significantly reduced the level of this marker. LLLT had a beneficial effect also on the skeletal muscle performance of
mdx
mice. However, the single application of LLLT and the dose parameters used in this study were not able to change the morphology of a dystrophic muscle. |
---|---|
ISSN: | 0268-8921 1435-604X |
DOI: | 10.1007/s10103-015-1777-7 |