Literature DB >> 3022724

Deficiency of subunits in heart mitochondrial NADH-ubiquinone oxidoreductase of a patient with mitochondrial encephalomyopathy and cardiomyopathy.

M Tanaka, M Nishikimi, H Suzuki, T Ozawa, M Nishizawa, K Tanaka, T Miyatake.   

Abstract

The heart mitochondria isolated from a patient with hypertrophic cardiomyopathy associated with mitochondrial encephalomyopathy were analyzed by immunoblotting using specific antibody against each of the purified mitochondrial energy transducing complexes from beef heart. Subunits of NADH-ubiquinone oxidoreductase (Complex I) were markedly decreased and those of cytochrome c oxidase (Complex IV) were decreased to some extent, but the deficiency of any of these subunits was only partial. On the other hand, the contents of subunits of ubiquinol-cytochrome c oxidoreductase (Complex III) were normal. These results suggest that the decreased levels of some of the Complex I subunits might be the primary cause of disorder in this patient.

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Year:  1986        PMID: 3022724     DOI: 10.1016/0006-291x(86)91061-2

Source DB:  PubMed          Journal:  Biochem Biophys Res Commun        ISSN: 0006-291X            Impact factor:   3.575


  7 in total

1.  Multiple respiratory chain abnormalities associated with hypertrophic cardiomyopathy and 3-methylglutaconic aciduria.

Authors:  H Ibel; W Endres; H B Hadorn; T Deufel; I Paetzke; M Duran; N G Kennaway; K M Gibson
Journal:  Eur J Pediatr       Date:  1993-08       Impact factor: 3.183

2.  Deficiency of subunits of complex I or IV in mitochondrial myopathies: immunochemical and immunohistochemical study.

Authors:  M Tanaka; M Nishikimi; H Suzuki; M Tada; T Ozawa; Y Koga; I Nonaka
Journal:  J Inherit Metab Dis       Date:  1987       Impact factor: 4.982

Review 3.  Molecular defects of NADH-ubiquinone oxidoreductase (complex I) in mitochondrial diseases.

Authors:  J A Morgan-Hughes; A H Schapira; J M Cooper; J B Clark
Journal:  J Bioenerg Biomembr       Date:  1988-06       Impact factor: 2.945

4.  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

5.  Fatal infantile mitochondrial cardiomyopathy and myopathy with heterogeneous tissue expression of combined respiratory chain deficiencies.

Authors:  J Müller-Höcker; H Ibel; I Paetzke; T Deufel; W Endres; B Kadenbach; J M Gokel; G Hübner
Journal:  Virchows Arch A Pathol Anat Histopathol       Date:  1991

6.  Chronic progressive external ophthalmoplegia in patients with large heteroplasmic mitochondrial DNA deletions: an immunocytochemical study.

Authors:  S Collins; X Dennett; E Byrne; S Marzuki
Journal:  Acta Neuropathol       Date:  1991       Impact factor: 17.088

Review 7.  The biochemical basis of mitochondrial diseases.

Authors:  H R Scholte
Journal:  J Bioenerg Biomembr       Date:  1988-04       Impact factor: 2.945

  7 in total

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