Eicosapentaenoic acid decreases TNF-α and protects dystrophic muscles of mdx mice from degeneration

J Neuroimmunol. 2011 Mar;232(1-2):145-50. doi: 10.1016/j.jneuroim.2010.10.032. Epub 2010 Dec 4.

Abstract

In dystrophin-deficient fibers of mdx mice and in Duchenne muscular dystrophy, inflammation and increased production of tumor necrosis factor alpha (TNF-α) contribute to myonecrosis. We examined the effects of eicosapentaenoic acid (EPA) on dystrophic muscle degeneration. Mdx mice (14 days old) received EPA for 16 days. The sternomastoid, diaphragm and biceps brachii muscles were removed. Control mdx mice received vehicle. EPA decreased creatine kinase and myonecrosis and reduced the levels of TNF-α. These results suggest that EPA plays a protective role in dystrophic muscle degeneration, possibly by reducing TNF-α, and support further investigations of EPA as a potential therapy for dystrophinopathies.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Blotting, Western
  • Creatine Kinase / analysis
  • Creatine Kinase / metabolism
  • Eicosapentaenoic Acid / therapeutic use*
  • Female
  • Male
  • Mice
  • Mice, Inbred mdx
  • Muscle, Skeletal / drug effects
  • Muscle, Skeletal / pathology
  • Muscular Dystrophy, Animal / drug therapy*
  • Muscular Dystrophy, Animal / metabolism
  • Muscular Dystrophy, Animal / pathology*
  • Necrosis / pathology
  • Tumor Necrosis Factor-alpha / biosynthesis*
  • Tumor Necrosis Factor-alpha / drug effects

Substances

  • Tumor Necrosis Factor-alpha
  • Eicosapentaenoic Acid
  • Creatine Kinase