A mathematical model of action potentials of mouse sinoatrial node cells with molecular bases

Sanjay Kharche, Jian Yu, Ming Lei, Henggui Zhang

    Research output: Contribution to journalArticlepeer-review


    Genetically modified mice are popular experimental models for studying the molecular bases and mechanisms of cardiac arrhythmia. A postgenome challenge is to classify the functional roles of genes in cardiac function. To unveil the functional role of various genetic isoforms of ion channels in generating cardiac pacemaking action potentials (APs), a mathematical model for spontaneous APs of mouse sinoatrial node (SAN) cells was developed. The model takes into account the biophysical properties of membrane ionic currents and intracellular mechanisms contributing to spontaneous mouse SAN APs. The model was validated by its ability to reproduce the physiological exceptionally short APs and high pacing rates of mouse SAN cells. The functional roles of individual membrane currents were evaluated by blocking their coding channels. The roles of intracellular Ca2+ handling mechanisms on cardiac pacemaking were also investigated in the model. The robustness of model pacemaking behavior was evaluated by means of one-and two-parameter analyses in wide parameter value ranges. This model provides a predictive tool for cellular level outcomes of electrophysiological experiments. It forms the basis for future model development and further studies into complex pacemaking mechanisms as more quantitative experimental data become available. © 2011 the American Physiological Society.
    Original languageEnglish
    Pages (from-to)H945-H963
    JournalAmerican Journal of Physiology: Heart and Circulatory Physiology
    Issue number3
    Publication statusPublished - Sept 2011


    • Cardiac action potential
    • Computer modeling
    • Genetic isoforms
    • Pacemaking mechanisms


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