首页> 外文期刊>European journal of heart failure: journal of the Working Group on Heart Failure of the European Society of Cardiology >Age-dependent changes in contractile function and passive elastic properties of myocardium from mice lacking muscle LIM protein (MLP)
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Age-dependent changes in contractile function and passive elastic properties of myocardium from mice lacking muscle LIM protein (MLP)

机译:缺乏肌肉LIM蛋白(MLP)的小鼠心肌收缩功能和被动被动弹性的年龄依赖性变化

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Aims: Muscle LIM protein (MLP) null mice are often used as a model for human dilated cardiomyopathy. So far, little is known about the time course and pathomechanisms leading to the development of the adult phenotype. Methods and results: We systematically analysed the contractile phenotype, myofilament calcium (Ca 2) responsiveness, passive myocardial mechanics, histology, and mRNA expression in mice aged 4 and 12 weeks. In 4-week-old animals, there was no significant difference in the forcefrequency relationship (FFR) and catecholamine response of intact isolated papillary muscles between wild-type (WT) and MLP null myocardium. In 12-week-old animals, WT myocardium exhibited a significantly positive FFR, while that of MLP null mice was significantly negative, and the inotropic response to catecholamines was significantly reduced in MLP null mice. This time course of decline in contractile function was confirmed in vivo by echocardiography. Whereas at 4 weeks of age MLP null mice and WT littermates showed similar levels of SERCA2a (sarcoplasmic reticulum Ca 2 ATPase) expression, the expression was significantly lower in 12-week-old MLP null mice compared with littermate controls. Myofilament Ca 2 responsiveness was not affected by the lack of MLP, irrespective of age. Whereas in 4-week-old animals MLP null myocardium showed a trend to an increased compliance compared with the WT, myocardium of 12-week-old MLP null mice was significantly less compliant than WT myocardium. Parallel to the decrease in compliance there was an increase in fibrosis in the MLP null animals. Conclusion: Our data suggest that MLP deficiency does not primarily influence myocardial contractility. A lack of MLP leads to an age-dependent impairment of excitationcontraction coupling with resulting contractile dysfunction and secondary fibrosis. Published on behalf of the European Society of Cardiology. All rights reserved.
机译:目的:肌肉LIM蛋白(MLP)无效的小鼠通常被用作人类扩张型心肌病的模型。迄今为止,关于导致成人表型发展的时间过程和致病机理知之甚少。方法和结果:我们系统地分析了4周和12周龄小鼠的收缩表型,肌丝钙(Ca 2)反应性,被动心肌力学,组织学和mRNA表达。在4周龄的动物中,野生型(WT)和MLP无效心肌之间完整的孤立乳头肌的力频率关系(FFR)和儿茶酚胺反应无明显差异。在12周龄的动物中,WT心肌表现出明显的FFR阳性,而MLP缺失小鼠的FFR显着阴性,MLP缺失小鼠对儿茶酚胺的肌力反应显着降低。通过超声心动图在体内证实了收缩功能下降的这个时间过程。在4周龄时,MLP缺失小鼠和WT同窝小鼠的SERCA2a(肌浆网Ca 2 ATPase)表达水平相似,而在12周龄的MLP缺失小鼠中,该表达水平明显低于同窝对照。不论年龄大小,缺乏MLP均不会影响肌丝Ca 2反应性。与WT相比,在4周龄动物中MLP无效心肌显示出顺应性增加的趋势,而12周龄MLP null小鼠的心肌的顺应性明显低于WT心肌。与顺应性降低平行的是,MLP无效动物的纤维化增加。结论:我们的数据表明MLP缺乏并不主要影响心肌收缩力。缺乏MLP会导致与年龄相关的兴奋收缩功能受损,并导致收缩功能障碍和继发性纤维化。代表欧洲心脏病学会出版。版权所有。

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