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Effects of the antiarrhythmic drug dofetilide on myocardial electrical activity: a computer modelling study

机译:抗心律不齐药物多非利特对心肌电活动的影响:计算机模拟研究

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Dofetilide selectively inhibits the rapid component of the delayed potassium current (I/sub Kr/). In this work, a mathematical model of dofetilide effects on I/sub Kr/ has been developed. This model has been incorporated to the Luo and Rudy (II) model of guinea pig ventricular action potential and the effect of different dofetilide concentrations on the action potential characteristics has been studied. Our results show that the steady-state block of I/sub Kr/ is dose-dependent with a block of 10%, 53% and 92% for 1 nM, 10 nM and 100 nM of dofetilide respectively (IC/sub 50/=8.7 nM). This increment of I/sub Kr/ block when the concentration increases induces a prolongation of APD also in a dose-dependent way. We observed prolongations of APD/sub 90/ of 13% and 28% for 10 nM and 100 nM of dofetilide respectively. In agreement with experimental results, the interaction between dofetilide and the receptor in the channel presents slow kinetics and reverse use-dependence in our model.
机译:多非利特有选择地抑制延迟钾电流(I / sub Kr /)的快速成分。在这项工作中,已经开发了多芬替利对I / sub Kr /的影响的数学模型。该模型已被纳入豚鼠心室动作电位的Luo和Rudy(II)模型中,并且研究了不同多芬替利浓度对动作电位特性的影响。我们的结果表明,I / sub Kr /的稳态阻滞与剂量有关,多芬替利1nM,10 nM和100 nM的阻滞分别为10%,53%和92%(IC / sub 50 / = 8.7 nM)。当浓度增加时,I / sub Kr /阻滞的这种增加也以剂量依赖性方式引起APD的延长。我们观察到10 nM和100 nM多芬替利的APD / sub 90 /分别延长了13%和28%。与实验结果一致,多芬利特和通道中的受体之间的相互作用在我们的模型中呈现出缓慢的动力学和反向的使用依赖性。

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