Literature DB >> 6821580

Mitochondrial functions in chronic spinal muscular atrophy.

J M Gobernado, M Gosalvez, C Cortina, M Lousa, C Riva, A Gimeno.   

Abstract

We determined the respiration rate, respiratory control and ADP/O ratios, with different substrates in mitochondria isolated from seven patients with chronic spinal muscular atrophy and compared them with normal human muscle. In all cases studied, a severe alteration of the respiratory control with variable derangement of oxidative phosphorylation was found. Similar findings have been described in other neuromuscular disorders including the so-called "mitochondrial myopathy". We believe that this disturbance of mitochondrial function is non specific and only the hypermetabolic syndrome of Luft could be considered biochemically as a "mitochondrial myopathy", a disorder selectively involving mitochondria of skeletal muscle.

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Year:  1980        PMID: 6821580      PMCID: PMC490598          DOI: 10.1136/jnnp.43.6.546

Source DB:  PubMed          Journal:  J Neurol Neurosurg Psychiatry        ISSN: 0022-3050            Impact factor:   10.154


  15 in total

1.  Familial non-progressive myopathy with muscle cramps after exercise. A new disease associated with cores in the muscle fibres.

Authors:  J Bethlem; J van Gool; W C Hülsmann; A E Meijer
Journal:  Brain       Date:  1966-09       Impact factor: 13.501

2.  Severe hypermetabolism with primary abnormality of skeletal muscle mitochondria.

Authors:  N A Haydar; H L Conn; A Afifi; N Wakid; S Ballas; K Fawaz
Journal:  Ann Intern Med       Date:  1971-04       Impact factor: 25.391

3.  A new mitochondrial myopathy in a patient with salt craving.

Authors:  A J Spiro; J W Prineas; C L Moore
Journal:  Arch Neurol       Date:  1970-03

4.  Familial "mitochondrial" myopathy. A myopathy associated with disordered oxidative metabolism in muscle fibres. 2. Biochemical findings.

Authors:  M Worsfold; D C Park; R J Pennington
Journal:  J Neurol Sci       Date:  1973-07       Impact factor: 3.181

5.  Mitochondrial functions in five cases of human neuromuscular disorders.

Authors:  A Gimeno; J L Trueba; M Blanco; M Gosalvez
Journal:  J Neurol Neurosurg Psychiatry       Date:  1973-10       Impact factor: 10.154

6.  Respiratory control and oxidative phosphorylation in the denervated muscle of patients with amyotrophic lateral sclerosis. Biochemical comparison with diabetes mellitus.

Authors:  V Ionăşescu; N Luca; O Vuia; V Popa
Journal:  Acta Neurol Scand       Date:  1968       Impact factor: 3.209

7.  Respiratory control and oxidative phosphorylation in the dystrophic muscle.

Authors:  V Ionăşescu; N Luca; O Vuia
Journal:  Acta Neurol Scand       Date:  1967       Impact factor: 3.209

8.  Myopathy with abnormal structure and function of muscle mitochondria.

Authors:  W C Hulsmann; J Bethlem; A E Meijer; P Fleury; J P Schellens
Journal:  J Neurol Neurosurg Psychiatry       Date:  1967-12       Impact factor: 10.154

9.  Skeletal muscle disease with abnormal mitochondria.

Authors:  G K van Wijngaarden; J Bethlem; A E Meijer; W C Hülsmann; C A Feltkamp
Journal:  Brain       Date:  1967-09       Impact factor: 13.501

10.  Ragged-red fibers. A biochemical and morphological study.

Authors:  J T Black; D Judge; L Demers; S Gordon
Journal:  J Neurol Sci       Date:  1975-12       Impact factor: 3.181

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  2 in total

Review 1.  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

2.  Altered intracellular Ca2+ homeostasis in nerve terminals of severe spinal muscular atrophy mice.

Authors:  Rocío Ruiz; Juan José Casañas; Laura Torres-Benito; Raquel Cano; Lucía Tabares
Journal:  J Neurosci       Date:  2010-01-20       Impact factor: 6.167

  2 in total

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