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J Neuroimmunol ; 232(1-2): 145-50, 2011 Mar.
Article in English | MEDLINE | ID: mdl-21131061

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.


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