Intracellular Ca dynamics in ventricular fibrillation
- 1 May 2004
- journal article
- research article
- Published by American Physiological Society in American Journal of Physiology-Heart and Circulatory Physiology
- Vol. 286 (5) , H1836-H1844
- https://doi.org/10.1152/ajpheart.00123.2003
Abstract
In the heart, membrane voltage (Vm) and intracellular Ca (Cai) are bidirectionally coupled, so that ionic membrane currents regulate Cai cycling and Cai affects ionic currents regulating action potential duration (APD). Although Cai reliably and consistently tracks Vm at normal heart rates, it is possible that at very rapid rates, sarcoplasmic reticulum Cai cycling may exhibit intrinsic dynamics. Non-voltage-gated Cai release might cause local alternations in APD and refractoriness that influence wavebreak during ventricular fibrillation (VF). In this study, we tested this hypothesis by examining the extent to which Cai is associated with Vm during VF. Cai transients were mapped optically in isolated arterially perfused swine right ventricles using the fluorescent dye rhod 2 AM while intracellular membrane potential was simultaneously recorded either locally with a microelectrode (5 preparations) or globally with the voltage-sensitive dye RH-237 (5 preparations). Mutual information (MI) is a quantitative statistical measure of the extent to which knowledge of one variable (Vm) predicts the value of a second variable (Cai). MI was high during pacing and ventricular tachycardia (VT; 1.13 ± 0.21 and 1.69 ± 0.18, respectively) but fell dramatically during VF (0.28 ± 0.06, P < 0.001). Cai at sites 4–6 mm apart also showed decreased MI during VF (0.63 ± 0.13) compared with pacing (1.59 ± 0.34, P < 0.001) or VT (2.05 ± 0.67, P < 0.001). Spatially, Cai waves usually bore no relationship to membrane depolarization waves during nonreentrant fractionated waves typical of VF, whereas they tracked each other closely during pacing and VT. The dominant frequencies of Vm and Cai signals analyzed by fast Fourier transform were similar during VT but differed significantly during VF. Cai is closely associated with Vm closely during pacing and VT but not during VF. These findings suggest that during VF, non-voltage-gated Cai release events occur and may influence wavebreak by altering Vm and APD locally.Keywords
This publication has 27 references indexed in Scilit:
- Frequency Analysis of Ventricular Fibrillation in Swine VentriclesCirculation Research, 2002
- Arrhythmia as a Result of Poor Intercellular Coupling in the Sinus Node: A Simulation StudyJournal of Theoretical Biology, 2001
- Spatiotemporal complexity of ventricular fibrillation revealed by tissue mass reduction in isolated swine right ventricle. Further evidence for the quasiperiodic route to chaos hypothesis.Journal of Clinical Investigation, 1997
- Conduction Block and Chaotic Dynamics in an Asymmetrical Model of Coupled Cardiac CellsJournal of Theoretical Biology, 1997
- Chaos in Weakly-coupled Pacemaker CellsJournal of Theoretical Biology, 1997
- Spontaneous Myocardial Calcium Oscillations:Journal of Cardiovascular Electrophysiology, 1993
- Statistical Data Analysis in the Computer AgeScience, 1991
- Role of calcium and the calcium channel in the initiation and maintenance of ventricular fibrillation.Circulation Research, 1990
- Calcium-dependent fluorescence transients during ventricular fibrillationAmerican Heart Journal, 1990
- Do calcium-dependent ionic currents mediate ischemic ventricular fibrillation?The American Journal of Cardiology, 1982