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Isolation of Human Atrial Myocytes for Simultaneous Measurements of Ca2+ Transients and Membrane Currents
Published on: July 3, 2013
Intracellular Ca dynamics in ventricular fibrillation
Chikaya Omichi1, Scott T Lamp, Shien-Fong Lin
1Division of Cardiology, Cedars-Sinai Medical Center and Center for Health Sciences, University of California-Los Angeles Cardiovascular Research Laboratory, David Geffen School of Medicine, UCLA, Los Angeles, California 90095-1760, USA.
Insights
During ventricular fibrillation (VF), intracellular calcium (Cai) dynamics become uncoupled from membrane voltage (Vm). This suggests non-voltage-gated calcium release may disrupt cardiac electrical activity and wave propagation.
Area of Science:
- Cardiac Electrophysiology
- Calcium Signaling
- Arrhythmia Mechanisms
Background:
- Membrane voltage (Vm) and intracellular calcium (Cai) are coupled in the heart, influencing action potential duration (APD).
- At rapid heart rates, sarcoplasmic reticulum Cai cycling may exhibit independent dynamics.
- Non-voltage-gated Cai release could alter local APD and refractoriness, potentially causing wavebreak during ventricular fibrillation (VF).
Purpose of the Study:
- To investigate the association between intracellular calcium (Cai) and membrane voltage (Vm) during ventricular fibrillation (VF).
- To determine if Cai dynamics are voltage-dependent during rapid cardiac rhythms.
Main Methods:
- Optical mapping of Cai transients using rhod 2 AM in isolated swine right ventricles.
- Simultaneous intracellular membrane potential recording via microelectrodes or voltage-sensitive dye RH-237.
- Quantitative analysis using mutual information (MI) to assess Vm-Cai association and frequency analysis (fast Fourier transform).
Main Results:
- Mutual information between Vm and Cai significantly decreased during VF compared to pacing and ventricular tachycardia (VT).
- Spatial correlation between Cai waves and Vm depolarization waves was lost during VF.
- Dominant frequencies of Vm and Cai signals differed significantly during VF, unlike during VT.
Conclusions:
- Intracellular calcium (Cai) is closely associated with membrane voltage (Vm) during normal pacing and VT, but not during VF.
- Findings suggest the occurrence of non-voltage-gated Cai release events during VF.
- These localized Cai releases may contribute to wavebreak by locally altering Vm and APD.
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.
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