Dynamical mechanisms of pacemaker generation in IK1- downregulated human ventricular myocytes: Insights from bifurcation analyses of a mathematical model

Abstract

Dynamical mechanisms of the biological pacemaker (BP) generation in human ventricular myocytes were investigated by bifurcation analyses of a mathematical model. Equilibrium points (EPs), periodic orbits, stability of EPs, and bifurcation points were determined as functions of bifurcation parameters, such as the maximum conductance of inward-rectifier K+ current (I K1), for constructing bifurcation diagrams. Stable limit cycles (BP activity) abruptly appeared around an unstable EP via a saddle-node bifurcation when IK1 was suppressed by 84.6%. After the bifurcation at which a stable EP disappears, the IK1-reduced system has an unstable EP only, which is essentially important for stable pacemaking. To elucidate how individual sarcolemmal currents contribute to EP instability and BP generation, we further explored the bifurcation structures of the system during changes in L-type Ca2+ channel current (ICa,L), delayed-rectifier K+ currents (IK), or Na+/Ca2+ exchanger current (INaCa). Our results suggest that 1), I Ca,L is, but IK or INaCa is not, responsible for EP instability as a requisite to stable BP generation; 2), IK is indispensable for robust pacemaking with large amplitude, high upstroke velocity, and stable frequency; and 3), INaCa is the dominant pacemaker current but is not necessarily required for the generation of spontaneous oscillations. © 2005 by the Biophysical Society.