Literature DB >> 8051938

Mitochondrial creatine kinase activity in patients with disturbed energy generation in muscle mitochondria.

J Smeitink1, W Ruitenbeek, R Sengers, R Wevers, T van Lith, F Trijbels.   

Abstract

Eleven patients with an established disturbance in muscle mitochondrial energy generation, in whom no defect in the pyruvate dehydrogenase complex or in the complexes of the respiratory chain could be detected, were investigated for a possible deficiency of mitochondrial creatine kinase (Mi-CK) (EC 2.7.3.2). Four patients with a defect in one of the complexes of the respiratory chain were also investigated for Mi-CK activity. In none of the investigated patients was Mi-CK deficiency found. Surprisingly, two of the four patients with a defect in one of the respiratory chain complexes showed enhanced activity of Mi-CK. It is concluded that Mi-CK deficiency is not frequently found as a primary defect in patients with disturbance in mitochondrial energy generation, but more patients should be examined to allow a definite conclusion.

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Year:  1994        PMID: 8051938     DOI: 10.1007/bf00735397

Source DB:  PubMed          Journal:  J Inherit Metab Dis        ISSN: 0141-8955            Impact factor:   4.982


  13 in total

Review 1.  Mitochondrial creatine kinase: a key enzyme of aerobic energy metabolism.

Authors:  M Wyss; J Smeitink; R A Wevers; T Wallimann
Journal:  Biochim Biophys Acta       Date:  1992-09-25

2.  A microspectrophotometric method for the determination of cytochrome oxidase.

Authors:  S J COOPERSTEIN; A LAZAROW
Journal:  J Biol Chem       Date:  1951-04       Impact factor: 5.157

3.  Mitochondrial myopathies: multiple enzyme defects in the respiratory chain.

Authors:  W Ruitenbeek; J M Trijbels; J C Fischer; R C Sengers; A J Janssen; C M Kerkhof
Journal:  J Inherit Metab Dis       Date:  1989       Impact factor: 4.982

4.  The localization of mitochondrial creatine kinase, and its use for the determination of the sidedness of submitochondrial particles.

Authors:  H R Scholte; P J Weijers; E M Wit-Peeters
Journal:  Biochim Biophys Acta       Date:  1973-02-16

5.  Pyruvate oxidation in rat and human skeletal muscle mitochondria.

Authors:  H Bookelman; J M Trijbels; R C Sengers; A J Janssen; J H Veerkamp; A M Stadhouders
Journal:  Biochem Med       Date:  1978-12

Review 6.  Mitochondrial myopathies. Clinical, morphological and biochemical aspects.

Authors:  R C Sengers; A M Stadhouders; J M Trijbels
Journal:  Eur J Pediatr       Date:  1984-02       Impact factor: 3.183

7.  A method for quantitative measurement of mitochondrial creatine kinase in human skeletal muscle.

Authors:  J Smeitink; R Wevers; J Hulshof; W Ruitenbeek; T van Lith; R Sengers; F Trijbels; C Korenke; T Wallimann
Journal:  Ann Clin Biochem       Date:  1992-03       Impact factor: 2.057

8.  Isolated and combined deficiencies of NADH dehydrogenase (complex I) in muscle tissue of children with mitochondrial myopathies.

Authors:  G C Korenke; H A Bentlage; W Ruitenbeek; R C Sengers; W Sperl; J M Trijbels; F J Gabreels; F A Wijburg; V Wiedermann; F Hanefeld
Journal:  Eur J Pediatr       Date:  1990-12       Impact factor: 3.183

Review 9.  Deficiency of the alpha and beta subunits of pyruvate dehydrogenase in a patient with lactic acidosis and unexpected sudden death.

Authors:  W Sperl; W Ruitenbeek; C M Kerkhof; R C Sengers; J M Trijbels; J P Guggenbichler; A J Janssen; J A Bakkeren
Journal:  Eur J Pediatr       Date:  1990-04       Impact factor: 3.183

10.  A mitochondrial encephalomyopathy: the first case with an established defect at the level of coenzyme Q.

Authors:  J C Fischer; W Ruitenbeek; F J Gabreëls; A J Janssen; W O Renier; R C Sengers; A M Stadhouders; H J ter Laak; J M Trijbels; J H Veerkamp
Journal:  Eur J Pediatr       Date:  1986-02       Impact factor: 3.183

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