Spatiotemporal Relationship Between Intracellular Ca Dynamics and Wave Fragmentation During Ventricular Fibrillation in Isolated Blood-Perfused Pig Hearts

Normal “master–slave” relationship between the action potential (AP) and intracellular Ca transient (CaiT) is sometimes altered during ventricular fibrillation (VF). The nature of AP/CaiT dissociation during VF and its role in inducing wavebreaks (WBs) remain unclear. We simultaneously mapped AP (RH237) and CaiT (Rhod-2) during VF in blood-perfused pig hearts. We computed AP and CaiT dominant frequency (DF) and CaiT delay in each AP cycle. We identified WBs as singularity points in AP phase movies and sites of conduction block (CB) as sites where an AP wavefront failed to propagate. We analyzed spatiotemporal relationship between abnormal AP/CaiT sequences and CB sites. We used a calcium chelator (BAPTA-AM) to abolish CaiT and test its involvement in WB formation. During VF, the DF difference between AP and CaiT was 10% of the respective values in 95% of pixels, and 80% of all CaiT upstrokes occurred during the initial 25% of the excitation cycle. Aberrant sequences of AP and CaiT occurred almost exclusively near CB sites but could be traced to normal wavefront sequences away from CB sites. Thus, apparent AP/CaiT dissociation was largely attributable to spatial uncertainty of the absolute position of block of each wave. BAPTA-AM reduced CaiT amplitude to 30.5 12.9% of control and the DF of AP from 12.2 1.6 to 10.4 1.3Hz (P 0.01), but did not significantly alter WB incidence (0.76 0.19 versus 0.72 0.19SP/mm). These results do not support presence of spontaneous, non–voltage-gated CaiTs during VF and suggest that AP/CaiT dissociation is a consequence rather than a cause of wave fragmentation. (Circ Res. 2007;101:e90-e101.)