Literature DB >> 62828

Erythrocyte ghosts (Na+ + K+) ATPase activity in Duchenne's dystrophy and myotonia.

I Niebrój-Dobosz.   

Abstract

In Duchenne muscular dystrophy the activity of (Na+ + K+)ATPase in erythrocyte ghosts is reduced and its reaction to ouabain is paradoxical both in low sodium and high sodium systems. No such changes were seen in a case of Becker dystrophy, in limb-girdle dystrophy, and in neurogenic atrophy of muscles. In myotonic dystrophy and congenital myotonia the activity of ATPase and its inhibition by ouabain were depressed.

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Year:  1976        PMID: 62828     DOI: 10.1007/BF00313489

Source DB:  PubMed          Journal:  J Neurol        ISSN: 0340-5354            Impact factor:   4.849


  57 in total

1.  Abnormalities in membrane microviscosity and ion transport in genetic muscular dystrophy.

Authors:  R I Sha'afi; S B Rodan; R L Hintz; S M Fernandez; G A Rodan
Journal:  Nature       Date:  1975-04-10       Impact factor: 49.962

2.  Lipoprotein nature of red cell adenosine triphosphatase.

Authors:  H J SCHATZMANN
Journal:  Nature       Date:  1962-11-17       Impact factor: 49.962

3.  Electron spin resonance studies of erythrocytes from patients with myotonic muscular dystrophy.

Authors:  D A Butterfield; D B Chesnut; A D Roses; S H Appel
Journal:  Proc Natl Acad Sci U S A       Date:  1974-03       Impact factor: 11.205

4.  The effect of phospholipids on the apparent activation energy of (Na+-K+)-ATPase.

Authors:  K Taniguchi; S Iida
Journal:  Biochim Biophys Acta       Date:  1972-08-09

Review 5.  Membrane phenomena.

Authors:  A Rothstein
Journal:  Annu Rev Physiol       Date:  1968       Impact factor: 19.318

6.  Myotonia induced by diazacholesterol: increased (Na+ + K+)-ATPase activity of erythrocyte ghosts and development of cataracts.

Authors:  J B Peter; R M Andiman; R L Bowman; T Nagatomo
Journal:  Exp Neurol       Date:  1973-12       Impact factor: 5.330

7.  Effects of cations on ouabain binding by intact human erythrocytes.

Authors:  J D Gardner; C Frantz
Journal:  J Membr Biol       Date:  1974       Impact factor: 1.843

8.  Protein kinase activity in erythrocyte ghosts of patients with myotonic muscular dystrophy.

Authors:  A D Roses; S H Appel
Journal:  Proc Natl Acad Sci U S A       Date:  1973-06       Impact factor: 11.205

9.  Erythrocyte abnormality in human myopathy.

Authors:  H D Brown; S K Chattopadhyay; A B Patel
Journal:  Science       Date:  1967-09-29       Impact factor: 47.728

10.  Sodium, potassium, and chloride fluxes in intercostal muscle from normal goats and goats with hereditary myotonia.

Authors:  R J Lipicky; S H Bryant
Journal:  J Gen Physiol       Date:  1966-09       Impact factor: 4.086

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  3 in total

Review 1.  Duchenne muscular dystrophy: pathogenetic aspects and genetic prevention.

Authors:  H Moser
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

2.  Erythrocyte ghost (Na+ + K+) ATPase activity in mice with hereditary muscular dystrophy (strain C57 BL/64J/dy).

Authors:  G Souweine; M O Rolland; I Maire; M C Donas
Journal:  J Neurol       Date:  1978-02-14       Impact factor: 4.849

3.  The sodium pump of erythrocytes from patients with Duchenne muscular dystrophy: effect of ouabain on the active sodium flux and on (Na+, K+)ATPase.

Authors:  G Souweine; J C Bernard; Y Lasne; J Lachanat
Journal:  J Neurol       Date:  1978-03-09       Impact factor: 4.849

  3 in total

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