Literature DB >> 8107707

Skeletal muscle mitochondrial myopathy as a cause of exercise intolerance in a horse.

S J Valberg1, G P Carlson, G H Cardinet, E K Birks, J H Jones, A Chomyn, S DiMauro.   

Abstract

Although exertional myopathies are commonly recognized in horses, specific etiologies have not been identified. This is the first report in the horse of a deficiency of Complex I respiratory chain enzyme associated with profound exercise intolerance. Physical examination, routine blood tests, endoscopy, and ultrasonograms of the heart and iliac arteries were unremarkable. With slow, incremental exercise (speeds 1.5-7 m/s), the Arabian mare showed a marked lactic acidosis, increased mixed venous PVO2, and little change in oxygen consumption. Muscle biopsies contained large accumulations of mitochondria with bizarre cristae formations. Biochemical analyses revealed a very low activity of the first enzyme complex in the mitochondrial respiratory chain (NADH CoQ reductase). The exercise intolerance and muscle stiffness in this horse were attributed to a profound lactic acidosis resulting from impaired oxidative energy metabolism during exercise.

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Year:  1994        PMID: 8107707     DOI: 10.1002/mus.880170308

Source DB:  PubMed          Journal:  Muscle Nerve        ISSN: 0148-639X            Impact factor:   3.217


  1 in total

1.  Altered mitochondrial oxidative phosphorylation capacity in horses suffering from polysaccharide storage myopathy.

Authors:  Irene Tosi; Tatiana Art; Dominique Cassart; Frédéric Farnir; Justine Ceusters; Didier Serteyn; Hélène Lemieux; Dominique-Marie Votion
Journal:  J Bioenerg Biomembr       Date:  2018-08-24       Impact factor: 2.945

  1 in total

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