首页> 外文期刊>Journal of Molecular and Cellular Cardiology >Numerical models based on a minimal set of sarcolemmal electrogenic proteins and an intracellular Ca2+ clock generate robust, flexible, and energy-efficient cardiac pacemaking
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Numerical models based on a minimal set of sarcolemmal electrogenic proteins and an intracellular Ca2+ clock generate robust, flexible, and energy-efficient cardiac pacemaking

机译:基于最小数量的肌膜上的肌电蛋白和细胞内Ca2 +时钟的数值模型可生成强大,灵活且节能的心脏起搏器

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Recent evidence supports the idea that robust and, importantly, FLEXIBLE automaticity of cardiac pacemaker cells is conferred by a coupled system of membrane ion currents (an "M-clock") and a sarcoplasmic reticulum (SR)-based Ca2+ oscillator ("Ca2+clock") that generates spontaneous diastolic Ca2+ releases. This study identified numerical models of a human biological pacemaker that features robust and flexible automaticity generated by a minimal set of electrogenic proteins and a Ca2+clock. Following the Occam's razor principle (principle of parsimony), M-clock components of unknown molecular origin were excluded from Maltsev-Lakatta pacemaker cell model and thirteen different model types of only 4 or 5 components were derived and explored by a parametric sensitivity analysis. The extended ranges of SR Ca2+ pumping (i.e. Ca2+clock performance) and conductance of ion currents were sampled, yielding a large variety of parameter combination, i.e. specific model sets. We tested each set's ability to simulate autonomic modulation of human heart rate (minimum rate of 50 to 70bpm; maximum rate of 140 to 210bpm) in response to stimulation of cholinergic and β-adrenergic receptors. We found that only those models that include a Ca2+clock (including the minimal 4-parameter model "ICaL+IKr+INCX+Ca2+clock") were able to reproduce the full range of autonomic modulation. Inclusion of If or ICaT decreased the flexibility, but increased the robustness of the models (a relatively larger number of sets did not fail during testing). The new models comprised of components with clear molecular identity (i.e. lacking IbNa & Ist) portray a more realistic pacemaking: A smaller Na+ influx is expected to demand less energy for Na+ extrusion. The new large database of the reduced coupled-clock numerical models may serve as a useful tool for the design of biological pacemakers. It will also provide a conceptual basis for a general theory of robust, flexible, and energy-efficient pacemaking based on realistic components.
机译:最近的证据支持这样的想法,即心脏起搏器细胞的鲁棒性,而且很重要的是,它是由膜离子电流(“ M-clock”)和基于肌质网(SR)的Ca2 +振荡器(“ Ca2 +时钟”)生成自发的舒张期Ca2 +释放。这项研究确定了一种人类生物起搏器的数值模型,该模型具有通过最少的一组电动蛋白质和Ca2 +时钟生成的强大而灵活的自动化功能。遵循Occam的剃刀原理(简约原则),从Maltsev-Lakatta起搏器细胞模型中排除了分子来源未知的M-clock组件,并通过参数敏感性分析得出并探索了13种不同的模型类型,其中只有4或5种组件。采样了SR Ca2 +泵的扩展范围(即Ca2 +时钟性能)和离子电流的电导率,从而产生了各种各样的参数组合,即特定的模型集。我们测试了每组响应于胆碱能受体和β-肾上腺素能受体刺激而模拟人类心律自主调节的能力(最小速率为50至70bpm;最大速率为140至210bpm)。我们发现,只有那些包含Ca2 +时钟的模型(包括最小的4参数模型“ ICaL + IKr + INCX + Ca2 + clock”)才能再现整个自主调制范围。包含If或ICaT会降低灵活性,但会增加模型的健壮性(测试过程中相对较多的设置不会失败)。新的模型由具有清晰分子身份(即缺乏IbNa和Ist)的组分组成,描绘出了更加现实的节奏:预计较小的Na +流入量将需要较少的能量进行Na +挤压。减少了耦合时钟数字模型的新大型数据库可以用作设计生物起搏器的有用工具。它还将为基于实际组件的稳健,灵活和节能起搏的一般理论提供概念基础。

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