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首页> 外文期刊>Circulation. Heart failure >Irregular rhythm adversely influences calcium handling in ventricular myocardium: implications for the interaction between heart failure and atrial fibrillation.
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Irregular rhythm adversely influences calcium handling in ventricular myocardium: implications for the interaction between heart failure and atrial fibrillation.

机译:不规则的节律会对心室心肌的钙处理产生不利影响:对心力衰竭和心房颤动之间相互作用的影响。

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Despite adequate rate control, the combination of atrial fibrillation with heart failure (HF) has been shown, in a number of studies, to hasten HF progression. In this context, we aimed to test the hypothesis that an irregular ventricular rhythm causes an alteration in ventricular cardiomyocyte excitation-contraction coupling which contributes to the progression of HF.We investigated the effects of electrical field stimulation (average frequency 2 Hz) in an irregular versus regular drive train pattern on the expression of calcium-handling genes and proteins in rat ventricular myocytes. The effect of rhythm on intracellular calcium transients was examined using Fura-2AM fluorescence spectroscopy. In conjunction, calcium-handling protein expression was examined in left ventricular samples obtained from end-stage HF patients, in patients with either persistent atrial fibrillation or sinus rhythm. Compared with regularly paced ventricular cardiomyocytes, in cells paced irregularly for 24 hours, there was a significant reduction in the expression of sarcoplasmic reticulum calcium (Ca(2+)) ATPase together with reduced serine-16 phosphorylation of phospholamban. These findings were accompanied by a 59% reduction (P<0.01) in the peak Ca2+ transient in irregulary paced myocytes compared with those with regular pacing. Consistent with these observations, we observed a 54% (P<0.05) decrease in sarcoplasmic reticulum Ca(2+)ATPase protein expression and an 85% (P<0.01) reduction in the extent of phosphorylation of phospholamban in the left ventricular myocardium of HF patients in atrial fibrillation compared with those in sinus rhythm.Together, these data demonstrate that ventricular rhythmicity contributes significantly to excitation-contraction coupling by altering the expression and activity of key calcium-handling proteins. These data suggest that control of rhythm may be of benefit in patients with HF.
机译:尽管有足够的心率控制,但多项研究显示房颤与心力衰竭(HF)的结合可加快HF的进展。在这种情况下,我们旨在检验假说,即不规则的心律会导致心室心肌细胞的兴奋-收缩耦合改变,从而导致HF的进展。我们研究了电场刺激(平均频率2 Hz)在不规则的情况下的作用。与常规传动系统模式相比,大鼠心室肌细胞中钙处理基因和蛋白质的表达使用Fura-2AM荧光光谱仪检查了节律对细胞内钙瞬变的影响。同时,在患有持续性心房颤动或窦性心律的心房纤颤末期患者的左心室样本中检查了钙处理蛋白的表达。与定期起搏的心室心肌细胞相比,在不规则起搏24小时的细胞中,肌浆网钙(Ca(2+))ATPase的表达显着减少,同时磷酸lamban的丝氨酸-16磷酸化也降低。与常规起搏相比,这些发现伴随着不规则起搏的心肌细胞中Ca2 +瞬时峰值降低了59%(P <0.01)。与这些观察结果一致,我们观察到肌浆网Ca(2+)ATPase蛋白表达降低了54%(P <0.05),而左室心肌磷脂酰肌醇的磷酸化程度降低了85%(P <0.01)。与窦性心律相比,心房颤动的心衰患者总体而言,这些数据表明,心律性通过改变关键的钙处理蛋白的表达和活性,对激发-收缩偶联起重要作用。这些数据表明,控制心律对HF患者可能有益。

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