Mitochondrial function is altered in horse atypical myopathy

Helene Lemieux, Francois Boemer, Gaby van Galen, Didier Serteyn, Helene Amory, Etienne Baise, Dominique Cassart, Gunther van Loon, Christel Marcillaud-Pitel, Dominique-Marie Votion

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningpeer review

17 Citationer (Scopus)

Abstract

Equine atypical myopathy in Europe is a fatal rhabdomyolysis syndrome that results from the ingestion of hypoglycin A contained in seeds and seedlings of Acer pseudoplatanus (sycamore maple). Acylcarnitine concentrations in serum and muscle OXPHOS capacity were determined in 15 atypical myopathy cases. All but one acylcarnitine were out of reference range and mitochondrial respiratory capacity was severely decreased up to 49% as compared to 10 healthy controls. The hallmark of atypical myopathy thus consists of a severe alteration in the energy metabolism including a severe impairment in muscle mitochondrial respiration that could contribute to its high death rate.
OriginalsprogEngelsk
TidsskriftMitochondrion
Vol/bind30
Sider (fra-til)35-41
Antal sider7
ISSN1567-7249
DOI
StatusUdgivet - sep. 2016
Udgivet eksterntJa

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