Computational methods for simulating biophysically detailed, large-sca
le models of mammalian cardiac sinus and atrial networks on the massiv
ely parallel Connection Machine CM-2, and techniques for visualization
of simulation data, are presented. Individual cells are modeled using
the formulations of Noble et al. Models incorporate properties of vol
tage-dependent membrane currents, ion pumps and exchangers, and intern
al calcium sequestering and release mechanisms. Network models are use
d to investigate factors determining the site of generation and direct
ion of propagation of the pacemaker potential. Models of the isolated
sinus node are used to show that very few gap junction channels are re
quired to support frequency entrainment. When cell membrane properties
in the isolated sinus node models are modified to reproduce regional
differences in oscillation properties, as described by the data of Kod
ama and Boyett, an excitatory wave is generated in the node periphery
which propagates towards the node center. This agrees with activation
patterns measured in the isolated sinus node by Kirchoff. When the mod
el sinus node is surrounded by a region of atrial cells, the site of p
acemaker potential generation is shifted away from the periphery towar
ds the node center. This is in agreement with activation patterns meas
ured by Kirchoff in the intact sinus node of the rabbit heart, and dem
onstrates the importance of sinus node boundary conditions on shaping
the site of generation and direction of propagation of the pacemaker p
otential.