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

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...

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Veröffentlicht in:Journal of neuroimmunology 2011-03, Vol.232 (1), p.145-150
Hauptverfasser: Machado, Rafael Ventura, Mauricio, Adriana Fogagnolo, Taniguti, Ana Paula Tiemi, Ferretti, Renato, Neto, Humberto Santo, Marques, Maria Julia
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Sprache:eng
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Zusammenfassung: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.
ISSN:0165-5728
1872-8421
DOI:10.1016/j.jneuroim.2010.10.032