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PMID: 6093035 Published · ppublish English Case Reports Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

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

Pediatric research ·Vol. 18 ·No. 10 ·1984-10-00 ·Pages 991-9

Kennaway NG, Buist NR, Darley-Usmar VM, Papadimitriou A, Dimauro S, Kelley RI, Capaldi RA, Blank NK, D'Agostino A

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 mumol/min/g tissue in whole muscle (controls 1.16 +/- 0.47 mumol/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 bc1 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.(ABSTRACT TRUNCATED AT 250 WORDS)

MeSH Terms
Acidosis/enzymology Adolescent Biopsy Electron Transport Complex III Female Humans Lactates/blood Microscopy, Electron Mitochondria, Muscle/enzymology,ultrastructure Multienzyme Complexes/deficiency Muscles/enzymology,pathology Muscular Diseases/enzymology,pathology NADH Dehydrogenase/deficiency NADH, NADPH Oxidoreductases/deficiency Quinone Reductases/deficiency Succinate Cytochrome c Oxidoreductase/deficiency Succinate Dehydrogenase/deficiency
Chemicals
Lactates Multienzyme Complexes Succinate Cytochrome c Oxidoreductase Succinate Dehydrogenase NADH, NADPH Oxidoreductases Quinone Reductases NADH Dehydrogenase Electron Transport Complex III
Authors & Affiliations
9 authors, click to expand affiliations / ORCID
Kennaway N G
Buist N R
Darley-Usmar V M
Papadimitriou A
Dimauro S
Kelley R I
Capaldi R A
Blank N K
D'Agostino A
Article Info
Journal
Pediatric research
Abbr.
Pediatr Res
ISSN
0031-3998
Published
1984-10-00
Pages
991-9
Language
English
Region
United States
NLM ID
0100714
Subset
IM
Grants
NHLBI NIH HHS · HC-22050 · United States
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