Literature DB >> 6093035

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

N G Kennaway, N R Buist, V M Darley-Usmar, A Papadimitriou, S Dimauro, R I Kelley, R A Capaldi, N K Blank, A D'Agostino.   

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)

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Year:  1984        PMID: 6093035     DOI: 10.1203/00006450-198410000-00017

Source DB:  PubMed          Journal:  Pediatr Res        ISSN: 0031-3998            Impact factor:   3.756


  27 in total

Review 1.  Mitochondrial myopathies.

Authors:  S DiMauro; E Bonilla; M Zeviani; S Servidei; D C DeVivo; E A Schon
Journal:  J Inherit Metab Dis       Date:  1987       Impact factor: 4.982

2.  Fatal hepatic failure with lactic acidaemia, Fanconi syndrome and defective activity of succinate:cytochrome c reductase.

Authors:  M A Vilaseca; P Briones; A Ribes; E Carreras; A Llácer; J Querol
Journal:  J Inherit Metab Dis       Date:  1991       Impact factor: 4.982

3.  Deficiency of complex III of the mitochondrial respiratory chain in a patient with facioscapulohumeral disease.

Authors:  D M Slipetz; J R Aprille; P R Goodyer; R Rozen
Journal:  Am J Hum Genet       Date:  1991-03       Impact factor: 11.025

4.  Defective pattern of mitochondrial respiratory enzymes in mitochondrial myopathy.

Authors:  S Miyabayashi; K Haginoya; H Hanamizu; K Iinuma; K Narisawa; K Tada
Journal:  J Inherit Metab Dis       Date:  1989       Impact factor: 4.982

5.  Exercise increases mitochondrial complex I activity and DRP1 expression in the brains of aged mice.

Authors:  Aaron M Gusdon; Jason Callio; Giovanna Distefano; Robert M O'Doherty; Bret H Goodpaster; Paul M Coen; Charleen T Chu
Journal:  Exp Gerontol       Date:  2017-01-18       Impact factor: 4.032

6.  Immunochemical study in three patients with cytochrome c oxidase deficiency presenting Leigh's encephalomyelopathy.

Authors:  S Miyabayashi; T Ito; D Abukawa; K Narisawa; K Tada; M Tanaka; T Ozawa; M Droste; B Kadenbach
Journal:  J Inherit Metab Dis       Date:  1987       Impact factor: 4.982

Review 7.  Disorders of the mitochondrial respiratory chain: clinical manifestations and diagnostic approach.

Authors:  J M Trijbels; R C Sengers; W Ruitenbeek; J C Fischer; J A Bakkeren; A J Janssen
Journal:  Eur J Pediatr       Date:  1988-11       Impact factor: 3.183

8.  Clinical and biochemical phenotype of the MELAS mutation.

Authors:  S Miyabayashi; H Hanamizu; R Nakamura; J I Hayashi; K Tada
Journal:  J Inherit Metab Dis       Date:  1993       Impact factor: 4.982

9.  Stability of frozen muscle used for mitochondrial enzyme assays.

Authors:  D A Applegarth; T Tong; L A Clarke
Journal:  Eur J Pediatr       Date:  1994-02       Impact factor: 3.183

10.  Investigation of enzyme defects in children with lactic acidosis.

Authors:  B Merinero; C Pérez-Cerda; M Ugarte
Journal:  J Inherit Metab Dis       Date:  1992       Impact factor: 4.982

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