Contractile properties of myocardium are altered in dystrophin-deficient mdx mice

John L. Sapp, Jacques Bobet, Susan E. Howlett

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33 Citas (Scopus)

Resumen

The objective of this study was to determine whether cardiac contractile force is altered in the dystrophin-deficient mdx mouse model of muscular dystrophy. Left atria from 12-14-week-old control and mdx mice were paced at 1 Hz in 1.25 mM external Ca2+ buffer. Twitch properties and effects of interposing intervals of 0.3 to 600 s on the force of subsequent beats (force-interval curves) were examined. Peak force and time-to-peak force were similar in both groups, but half-relaxation time was significantly prolonged in mdx heart. In control hearts, force-interval curves increased to an inflection point at about 1 s, then rose to a second peak near 60 s. In mdx heart, curves reached the early inflection more quickly, the second peak was diminished in magnitude and force was greatly depressed at long intervals. Curves were fitted to a four-parameter equation to quantify differences in shape. The parameter a, which reflects rate of rise to the first inflection, was significantly increased in mdx atria, while the parameter B, which reflects amplitude of the late peak, was significantly reduced. These differences in force production were more marked when external Ca2+ was raised to 2.5 mM. Results show contractile properties are markedly altered in atria from dystrophin-deficient mdx mice. These findings are consistent with the hypothesis that dystrophin deficiency affects cardiac contractile function, possibly through effects on SR function.

Idioma originalEnglish
Páginas (desde-hasta)17-24
Número de páginas8
PublicaciónJournal of the Neurological Sciences
Volumen142
N.º1-2
DOI
EstadoPublished - oct. 1996

Nota bibliográfica

Funding Information:
These studies were funded by the Heart and Stroke Foundation of Canada, the Muscular Dystrophy Association of Canada and the MRC. S.E.H. was a Scholar of the Heart and Stroke Foundation of Canada during the period of this study. J.L.S. was partially funded through a Dalhousie Faculty of Medicine summer studentship award. The authors wish to thank Peter Nicholl for excellent technical assistance and Dr. G.R. Ferrier for helpful comments.

ASJC Scopus Subject Areas

  • Neurology
  • Clinical Neurology

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