Literature DB >> 75952

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

G Souweine, M O Rolland, I Maire, M C Donas.   

Abstract

Erythrocyte ghost (Na+ + K+) ATPase activity was studied in mice with hereditary muscular dystrophy (strain C 57 BL 6J/dy) and appropriate controls. No difference was observed in the enzymatic activity between dystrophic and any of the healthy genotypes. Ouabain 5 mM and 0.1 mM inhibited the enzymatic activity and no difference was observed between dystrophic and control animals. The results are discussed in the light of the literature.

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Year:  1978        PMID： 75952     DOI： 10.1007/BF00312959

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


  44 in total

1.  Erythrocyte deformation in duchenne muscular dystrophy.

Authors:  E M Lumb; A E Emery
Journal:  Br Med J       Date:  1975-08-23

2.  [Aldolase excess in blood in myopathic mice].

Authors:  F SCHAPIRA; G SCHAPIRA; J C DREYFUS
Journal:  C R Hebd Seances Acad Sci       Date:  1957-08-05

3.  Concentrations of K and Na in skeletal muscle of mice with a hereditary myopathy (Dystrophia muscularis).

Authors:  N BAKER; W H BLAHD; P HART
Journal:  Am J Physiol       Date:  1958-06

4.  Apparent alterations of erythrocyte acetylcholinesterase and other membrane proteins in Duchenne muscular dystrophy: a further example of a generalized membrane defect associated with hereditary muscular dystrophy.

Authors:  P K Das; D Graesslin; H W Goedde
Journal:  Biochem Soc Trans       Date:  1976       Impact factor: 5.407

5.  Erythrocytes in human muscular dystrophy.

Authors:  T D Miale; J L Frias; D L Lawson
Journal:  Science       Date:  1975-02-07       Impact factor: 47.728

6.  Scanning electron microscopy studies in muscular dystrophy.

Authors:  S E Miller; A D Roses; S H Appel
Journal:  Arch Neurol       Date:  1976-03

7.  An altered erythrocyte acetylcholinesterase associated with hereditary muscular dystrophy in mice.

Authors:  P K Das; R L Watts; D C Watts
Journal:  Biochem J       Date:  1971-07       Impact factor: 3.857

8.  Erythrocyte shape in Duchenne muscular dystrophy.

Authors:  D W Matheson; W K Engel; E C Derrer
Journal:  Neurology       Date:  1976-12       Impact factor: 9.910

9.  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

10.  Membrane adenosine triphosphatase as a participant in the active transport of sodium and potassium in the human erythrocyte.

Authors:  R L POST; C R MERRITT; C R KINSOLVING; C D ALBRIGHT
Journal:  J Biol Chem       Date:  1960-06       Impact factor: 5.157
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  2 in total

Review 1.  Role of intracellular calcium in promoting muscle damage: a strategy for controlling the dystrophic condition.

Authors:  C J Duncan
Journal:  Experientia       Date:  1978-12-15

2.  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
  2 in total

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