Literature DB >> 3406942

Ultrastructural changes in the cardiomyopathy of dystrophic hamsters and mice.

M F Rudge1, C J Duncan.   

Abstract

Changes in the ultrastructure of the cardiac muscle cells have been followed in dystrophic mice and hamsters (22-40 weeks of age) and in both species a severe cardiomyopathy accompanies the cellular damage of the skeletal muscle. The degradative changes of the myofilament apparatus of the heart cells and the specific changes in mitochondrial ultrastructure (including swelling, septation and apparent division) are characteristic of the cellular damage of both the dystrophic skeletal muscle and of normal cardiac muscle in which [Ca]i has been experimentally raised, confirming the suggestions that (i) the same gene is responsible for the myopathy of skeletal and cardiac muscle in animal dystrophy and (ii) that changes in [Ca]i are implicated in the degradative changes of muscle cells.

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Year:  1988        PMID: 3406942     DOI: 10.1016/0040-8166(88)90046-8

Source DB:  PubMed          Journal:  Tissue Cell        ISSN: 0040-8166            Impact factor:   2.466


  1 in total

1.  Dystrophin deficiency in Drosophila reduces lifespan and causes a dilated cardiomyopathy phenotype.

Authors:  Ouarda Taghli-Lamallem; Takeshi Akasaka; Grant Hogg; Uri Nudel; David Yaffe; Jeffrey S Chamberlain; Karen Ocorr; Rolf Bodmer
Journal:  Aging Cell       Date:  2008-01-23       Impact factor: 9.304

  1 in total

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