Abstract

Reactive oxygen species (ROS) are generated in skeletal muscle both during the rest and contractile activity. Myogenic cells are equipped with antioxidant enzymes, like superoxide dismutase, catalase, glutathione peroxidase, γ-glutamylcysteine synthetase and heme oxygenase-1. These enzymes not only neutralise excessive ROS, but also affect myogenic regeneration at several stages: influence post-injury inflammatory reaction, enhance viability and proliferation of muscle satellite cells and myoblasts and affect their differentiation. Finally, antioxidant enzymes regulate also processes accompanying muscle regeneration—induce angiogenesis and reduce fibrosis. Elevated ROS production was also observed in Duchenne muscular dystrophy (DMD), a disease characterised by degeneration of muscle tissue and therefore—increased rate of myogenic regeneration. Antioxidant enzymes are consequently considered as target for therapies counteracting dystrophic symptoms. In this review we present current knowledge regarding the role of oxidative stress and systems of enzymatic antioxidant defence in muscular regeneration after both acute injury and persistent muscular degeneration.

Highlights

  • Reactive oxygen species (ROS) are generated in skeletal muscle both during the rest and contractile activity

  • Myogenic cells are equipped with antioxidant enzymes, like superoxide dismutase, catalase, glutathione peroxidase, c-glutamylcysteine synthetase and heme oxygenase-1

  • Elevated ROS production was observed in Duchenne muscular dystrophy (DMD), a disease characterised by degeneration of muscle tissue and — increased rate of myogenic regeneration

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Summary

REVIEW ARTICLE

The role of oxidative stress in skeletal muscle injury and regeneration: focus on antioxidant enzymes. This article is published with open access at Springerlink.com

Generation of reactive oxygen species in skeletal muscle
Major antioxidant systems in skeletal muscle
Oxidative stress in Duchenne muscular dystrophy
Antioxidant enzymes in DMD
Findings
Conclusions

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