Simurda J, Simurdová M, Bravený P, Christé G
Department of Physiology, Masaryk University, Brno, Czech Republic.
Mol Cell Biochem. 1996 Jul-Aug;160-161:5-12. doi: 10.1007/BF00240025.
A quantitative model of Ca-turnover in cardiac cells that incorporates negative feedback modulation of sarcolemmal calcium transport (via Ca channels and Na/Ca exchange) has been designed. The Na/Ca exchange current was expressed as INaCa = INaCar + delta INaCa. The component INaCar reflects slow changes of Ca2+ and Na+ concentrations and depends on the Na/K pump. delta INaCa is the fast component related to the Ca2+ transient. The single input to the model is an arbitrary sequence of intervals between excitations; outputs are sequences of calcium amounts transferred among the compartments during individual intervals. The model operates with a combination of discrete variables (amounts of Ca transferred during contraction, relaxation and rest) and continuous variables - slow changes in ionic concentrations. Since the model is not formalistic but respects the nature of the underlying elements of the system, it enables us to stimulate the known effects of cardiotropic drugs or to predict their unknown mechanisms by visualizing the changes in individual Ca compartments. By altering the parameters, the model also stimulates the known species and tissue differences in rate-dependent phenomena.
已设计出一种心肌细胞钙周转的定量模型,该模型纳入了肌膜钙转运(通过钙通道和钠/钙交换)的负反馈调节。钠/钙交换电流表示为INaCa = INaCar + δINaCa。INaCar成分反映了Ca2+和Na+浓度的缓慢变化,并依赖于钠/钾泵。δINaCa是与钙瞬变相关的快速成分。该模型的唯一输入是兴奋之间任意的间隔序列;输出是各个间隔期间各隔室之间转移的钙量序列。该模型结合离散变量(收缩、舒张和静息期间转移的钙量)和连续变量——离子浓度的缓慢变化进行运作。由于该模型并非形式化的,而是尊重系统潜在元素的性质,因此它使我们能够通过可视化各个钙隔室的变化来模拟已知的强心药物效应或预测其未知机制。通过改变参数,该模型还能模拟已知的速率依赖性现象中的物种和组织差异。