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

被引:32
作者
Sapp, JL
Bobet, J
Howlett, SE
机构
[1] DALHOUSIE UNIV,DEPT PHARMACOL,HALIFAX,NS B3H 4H7,CANADA
[2] UNIV ALBERTA,DEPT PHYS THERAPY,EDMONTON,AB T6G 2G4,CANADA
基金
英国医学研究理事会;
关键词
mdx mouse; dystrophin; muscular dystrophy; cardiac muscle; force-interval relation;
D O I
10.1016/0022-510X(96)00167-0
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
The objective of this study was to determine whether cardiac contractile force is altered in the dystrophin-deficient mdr 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.
引用
收藏
页码:17 / 24
页数:8
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