王 萌, 张季谦, 马文洋, 李 翔. 计算机模拟异常血钾浓度对兔窦房结起搏活性的影响及其调控[J]. 心脏杂志, 2012, 24(2): 146-149.
    引用本文: 王 萌, 张季谦, 马文洋, 李 翔. 计算机模拟异常血钾浓度对兔窦房结起搏活性的影响及其调控[J]. 心脏杂志, 2012, 24(2): 146-149.
    Effect of abnormal K+ concentration on pacemaker activity of rabbit sinoatrial node and its control by computer simulation[J]. Chinese Heart Journal, 2012, 24(2): 146-149.
    Citation: Effect of abnormal K+ concentration on pacemaker activity of rabbit sinoatrial node and its control by computer simulation[J]. Chinese Heart Journal, 2012, 24(2): 146-149.

    计算机模拟异常血钾浓度对兔窦房结起搏活性的影响及其调控

    Effect of abnormal K+ concentration on pacemaker activity of rabbit sinoatrial node and its control by computer simulation

    • 摘要: 目的:研究不同血钾浓度水平对窦房结电生理活性的影响,以及在血钾异常条件下,钠、钙离子浓度及钙电流对窦房结起搏的调控作用。方法:以Zhang构建的兔子窦房结仿真模型为研究对象,通过改变模型中钾、钠、钙离子通道的电导及钾、钠离子的浓度等参数,对模型满足的微分方程进行数值计算。结果:检验了异常血钾浓度对窦房结电生理活性的影响;发现在高血钾条件下,血钠变化对起搏活性有明显的调节作用;在血钾浓度异常条件下,增大L和T型钙电流,可以有效地恢复窦房结活性。结论:模拟实验显示,适当提高血钠的浓度,可以调控高血钾条件下的窦房结活性;提高钙通道的活性,可以有效地改善血钾浓度异常条件下的窦房结起搏活动。

       

      Abstract: AIM:To study the effect of different potassium ion concentrations on the electrophysiological activity of the sinoatrial node (SAN) and the control of Na+ and Ca2+ on the pacemaker activity of SAN under the condition of abnormal K+ concentration. METHODS: We used the Zhang model of the rabbit SAN. By changing the conductance of K+, Na+ and Ca2+, as well as their concentration, numerical calculations were then performed on the differential equations for this dynamic model. RESULTS: The effect of abnormal K+ concentration on electrophysiology of SAN was confirmed. It was found that under the hyperkalemia condition, changes in serum Na+ induced a significant regulating effect on pacing activity. Under the condition of abnormal K+ concentration, it restored pacemaker and conduction activity of SAN when increasing the L- and T-type Ca2+ current. CONCLUSION: Elevating Na+ concentration can enhance the activity of the SAN. Furthermore, pacemaker activity of SAN with abnormal K+ concentration can be effectively improved by increasing the activity of Ca2+ channels.

       

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