Lactic acidosis and mitochondrial myopathy associated with deficiency of several components of complex III of the respiratory chain

Nancy G. Kennaway, Neil R.M. Buist, Victor M. Darley-Usmar, Alexander Papadimitriou, Salvatore Dimauro, Richard I. Kelley, Roderick A. Capaldi, Nathan K. Blank, Anthony D'agostino

Research output: Contribution to journalArticlepeer-review

Abstract

We have studied a 17–year–old girl with lactic acidosis (3–18 mEq/liter) and progressive muscle weakness since 9 years of age. Morphological findings in muscle were of a typical ragged red myopathy with multiple collections of bizarre mitochondria, some containing paracrystalline inclusions. The carnitine content of serum and muscle was normal, as were the activities of carnitine palmitoyltransferase, carnitine octanoyltransferase, and carnitine acetyltransferase in the patient's muscle. Measurement of the enzymes of oxidative phosphorylation in both crude muscle homogenates and mitochondrial fractions showed close to normal activities of cytochrome c oxidase, succinate dehydrogenase, and ATPase. In contrast, succinate cytochrome c reductase activity was greatly reduced in the patient, being 0.035 μmol/min/g tissue in whole muscle (controls 1.16 ± 0.47 μmol/min/g tissue) and 8 nmol/min/mg protein in the mitochondria (control, 340 nmol/min/mg protein). Rotenonesensitive NADH–cytochrome c reductase was also undetectable in the patient's mitochondria. Spectral analysis of cytochromes showed decrease of reducible cytochrome b to 16% of the control. These results indicate a defect of ubiquinol–cytochrome c reductase or the cytochrome bc 1 segment (complex III) of the electron transport chain. Antibody–binding studies of the individual components of complex III showed additional deficiencies of core proteins I and II and peptide VI, indicating a more widespread defect of complex III than was evident from spectral analysis and enzyme activity measurements alone. Urine organic acid analysis after fasting and following a medium chain triglyceride load showed unusually high levels of lactate and 3–hydroxybutyrate, lower than expected levels of acetoacetate and dicarboxylic acids, and the presence of several other metabolites suggesting a disturbed citric acid cycle and redox state. Thus, the defect in this patient may be more widespread than is apparent from the clinical presentation.

Original languageEnglish (US)
Pages (from-to)991-999
Number of pages9
JournalPediatric research
Volume18
Issue number10
DOIs
StatePublished - Oct 1984
Externally publishedYes

ASJC Scopus subject areas

  • Pediatrics, Perinatology, and Child Health

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