A mitochondrial myopathy with a deficiency of respiratory chain NADH-CoQ reductase activity

J Neurol Sci. 1979 Sep;43(1):27-46. doi: 10.1016/0022-510x(79)90071-6.

Abstract

This paper presents data on two sisters with a mitochondrial myopathy characterised by weakness, marked exercise intolerance and a fluctuating lactic acidaemia. Both patients also experienced episodes of increased weakness which could be brought on by unaccustomed activity, going without food or by taking small quantities of alcohol. Metabolic studies during exercise showed a marked and sudden rise in blood lactate and pyruvate levels. Biochemical studies in one case showed that mitochondrial respiratory rates were markedly decreased with all NAD-linked substrates tested but were normal with succinate and with TMPD + ascorbate. The mitochondrial cytochrome components were normal as determined by low temperature spectroscopy and the addition of uncoupler did not enhance state 3 respiratory rates utilising NAD-linked substrates. It was concluded, therefore, that the mitochondrial lesion was located at the level of the NADH-CoQ reductase complex.

Publication types

  • Case Reports

MeSH terms

  • Adult
  • Chemical Phenomena
  • Chemistry
  • Cytochrome Reductases / deficiency*
  • Electron Transport
  • Female
  • Humans
  • Mitochondria, Muscle / enzymology*
  • Mitochondria, Muscle / ultrastructure
  • Muscular Diseases / enzymology*
  • Muscular Diseases / genetics
  • Muscular Diseases / pathology
  • NADH, NADPH Oxidoreductases / deficiency*
  • Physical Exertion
  • Quinone Reductases / deficiency*
  • Ubiquinone

Substances

  • Ubiquinone
  • NADH, NADPH Oxidoreductases
  • Cytochrome Reductases
  • Quinone Reductases