Exercise increases utrophin protein expression in the mdx mouse model of Duchenne muscular dystrophy

Muscle Nerve. 2014 Jun;49(6):915-8. doi: 10.1002/mus.24151.

Abstract

Introduction: Duchenne muscular dystrophy (DMD) is a lethal genetic disease caused by mutations in the dystrophin gene resulting in chronic muscle damage, muscle wasting, and premature death. Utrophin is a dystrophin protein homologue that increases dystrophic muscle function and reduces pathology. Currently, no treatments that increase utrophin protein expression exist. However, exercise increases utrophin mRNA expression in healthy humans. Therefore, the purpose was to determine whether exercise increases utrophin protein expression in dystrophic muscle.

Methods: Utrophin protein was measured in the quadriceps and soleus muscles of mdx mice after 12 weeks of voluntary wheel running exercise or sedentary controls. Muscle pathology was measured in the quadriceps.

Results: Exercise increased utrophin protein expression 334 ± 63% in the quadriceps relative to sedentary controls. Exercise increased central nuclei 4 ± 1% but not other measures of pathology.

Conclusions: Exercise may be an intervention that increases utrophin expression in patients with DMD.

Keywords: dystrophin; genetic disease; skeletal muscle; therapy; treatment.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • Disease Models, Animal
  • Female
  • Gene Expression
  • Male
  • Mice
  • Mice, Inbred mdx
  • Muscle, Skeletal / metabolism*
  • Muscle, Skeletal / pathology
  • Muscle, Skeletal / physiopathology
  • Muscular Dystrophy, Duchenne / metabolism*
  • Muscular Dystrophy, Duchenne / pathology
  • Muscular Dystrophy, Duchenne / physiopathology
  • Physical Conditioning, Animal / physiology*
  • RNA, Messenger / metabolism
  • Utrophin / metabolism*

Substances

  • RNA, Messenger
  • Utrophin