Improved guinea-pig ventricular cell model incorporating a diadic space, IKr and IKs, and length- and tension-dependent processes.

The guinea-pig ventricular cell model, originally developed by Noble et al in 1991, has been greatly extended to include accumulation and depletion of calcium in a diadic space between the sarcolemma and the sarcoplasmic reticulum where, according to contempory understanding, the majority of calcium-induced calcium release is triggered. The calcium in this space is also assumed to play the major role in calcium-induced inactivation of the calcium current. Delayed potassium current equations have been developed to include the rapid (IKr) and slow (IKs) components of the delayed rectifier current based on the data of of Heath and Terrar, along with data from Sanguinetti and Jurkiewicz. Length- and tension-dependent changes in mechanical and electrophysiological processes have been incorporated as described recently by Kohl et al. Drug receptor interactions have started to be developed, using the sodium channel as the first target. The new model has been tested against experimental data on action potential clamp, and on force-interval and duration-interval relations; it has been found to reliably reproduce experimental observations.

[1]  J. Koch-weser,et al.  THE INFLUENCE OF THE INTERVAL BETWEEN BEATS ON MYOCARDIAL CONTRACTILITY. , 1963, Pharmacological reviews.

[2]  B. Katzung,et al.  Time- and voltage-dependent interactions of antiarrhythmic drugs with cardiac sodium channels. , 1977, Biochimica et biophysica acta.

[3]  D. Noble,et al.  Excitation-contraction coupling and extracellular calcium transients in rabbit atrium: reconstruction of basic cellular mechanisms , 1987, Proceedings of the Royal Society of London. Series B. Biological Sciences.

[4]  D. Noble,et al.  A model of the single atrial cell: relation between calcium current and calcium release , 1990, Proceedings of the Royal Society of London. B. Biological Sciences.

[5]  M. Sanguinetti,et al.  Two components of cardiac delayed rectifier K+ current. Differential sensitivity to block by class III antiarrhythmic agents , 1990, The Journal of general physiology.

[6]  D. Noble,et al.  The Role of Sodium ‐ Calcium Exchange during the Cardiac Action Potential a , 1991, Annals of the New York Academy of Sciences.

[7]  P. Gage,et al.  A persistent sodium current in rat ventricular myocytes. , 1992, The Journal of physiology.

[8]  R L Winslow,et al.  Generation and propagation of ectopic beats induced by spatially localized Na–K pump inhibition in atrial network models , 1993, Proceedings of the Royal Society of London. Series B: Biological Sciences.

[9]  Y. Lai,et al.  Generation and propagation of normal and abnormal pacemaker activity in network models of cardiac sinus node and atrium , 1995 .

[10]  M. Boyett,et al.  The role of the Na(+)‐Ca2+ exchanger in the rate‐dependent increase in contraction in guinea‐pig ventricular myocytes. , 1995, The Journal of physiology.

[11]  D A Terrar,et al.  Separation of the components of the delayed rectifier potassium current using selective blockers of IKr and IKs in guinea‐pig isolated ventricular myocytes , 1996, Experimental physiology.

[12]  G. Gintant,et al.  Two components of delayed rectifier current in canine atrium and ventricle. Does IKs play a role in the reverse rate dependence of class III agents? , 1996, Circulation research.

[13]  D A Terrar,et al.  The deactivation kinetics of the delayed rectifier components IKr and IKs in guinea‐pig isolated ventricular myocytes , 1996, Experimental physiology.

[14]  M. Cannell,et al.  Ca2+ influx during the cardiac action potential in guinea pig ventricular myocytes. , 1996, Circulation research.

[15]  G. Langer,et al.  Calcium concentration and movement in the diadic cleft space of the cardiac ventricular cell. , 1996, Biophysical journal.

[16]  K. Linz,et al.  Modulation of L-type calcium current by internal potassium in guinea pig ventricular myocytes. , 1997, Cardiovascular research.

[17]  D. Noble,et al.  Modeling of internal pH, ion concentration, and bioenergetic changes during myocardial ischemia. , 1997, Advances in experimental medicine and biology.

[18]  P Kohl,et al.  Cellular mechanisms of cardiac mechano-electric feedback in a mathematical model. , 1998, The Canadian journal of cardiology.

[19]  D Noble,et al.  Modelling of sodium-overload arrhythmias and their suppression. , 1998, The Canadian journal of cardiology.