N-Acetylcysteine Reduces Skeletal Muscles Oxidative Stress and Improves Grip Strength in Dysferlin-Deficient Bla/J Mice.
Paz García-CamposXimena Báez-MatusCarlos Jara-GutiérrezMarilyn Paz-AraosCésar AstorgaLuis A CeaViviana RodríguezJorge A BevilacquaPablo CaviedesAna María CárdenasPublished in: International journal of molecular sciences (2020)
Dysferlinopathy is an autosomal recessive muscular dystrophy resulting from mutations in the dysferlin gene. Absence of dysferlin in the sarcolemma and progressive muscle wasting are hallmarks of this disease. Signs of oxidative stress have been observed in skeletal muscles of dysferlinopathy patients, as well as in dysferlin-deficient mice. However, the contribution of the redox imbalance to this pathology and the efficacy of antioxidant therapy remain unclear. Here, we evaluated the effect of 10 weeks diet supplementation with the antioxidant agent N-acetylcysteine (NAC, 1%) on measurements of oxidative damage, antioxidant enzymes, grip strength and body mass in 6 months-old dysferlin-deficient Bla/J mice and wild-type (WT) C57 BL/6 mice. We found that quadriceps and gastrocnemius muscles of Bla/J mice exhibit high levels of lipid peroxidation, protein carbonyls and superoxide dismutase and catalase activities, which were significantly reduced by NAC supplementation. By using the Kondziela's inverted screen test, we further demonstrated that NAC improved grip strength in dysferlin deficient animals, as compared with non-treated Bla/J mice, without affecting body mass. Together, these results indicate that this antioxidant agent improves skeletal muscle oxidative balance, as well as muscle strength and/or resistance to fatigue in dysferlin-deficient animals.
Keyphrases
- wild type
- oxidative stress
- skeletal muscle
- high fat diet induced
- transcription factor
- muscular dystrophy
- klebsiella pneumoniae
- dna damage
- multiple sclerosis
- end stage renal disease
- ischemia reperfusion injury
- type diabetes
- stem cells
- genome wide
- induced apoptosis
- high throughput
- depressive symptoms
- dna methylation
- physical activity
- weight loss
- smoking cessation
- binding protein
- multidrug resistant