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Intracellular Ca dynamics in ventricular fibrillation

Authors
 Chikaya Omichi  ;  Scott T. Lamp  ;  James N. Weiss  ;  Peng-Sheng Chen  ;  Alan Garfinkel  ;  Zhilin Qu  ;  Boris Kogan  ;  Hrayr S. Karagueuzian  ;  Moon-Hyoung Lee  ;  Mina Attin  ;  Shengmei Zhou  ;  Ali Baher  ;  Junzhong Yang  ;  Shien-Fong Lin 
Citation
 AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, Vol.286(5) : 1836-1844, 2004 
Journal Title
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY
ISSN
 0363-6135 
Issue Date
2004
MeSH
Animals ; Calcium/metabolism* ; Cardiac Pacing, Artificial ; Electrophysiology ; Female ; Fluorescent Dyes ; Fourier Analysis ; Heterocyclic Compounds, 3-Ring ; Intracellular Membranes/metabolism* ; Male ; Membrane Potentials ; Models, Cardiovascular ; Pyridinium Compounds ; Swine ; Tachycardia, Ventricular/physiopathology ; Ventricular Fibrillation/metabolism ; Ventricular Fibrillation/physiopathology*
Keywords
calcium transient ; action potential ; cardiac restitution ; optical mapping
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.
Files in This Item:
T200404865.pdf Download
DOI
10.1152/ajpheart.00123.2003
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers
Yonsei Authors
Lee, Moon-Hyoung(이문형) ORCID logo https://orcid.org/0000-0002-7268-0741
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/113016
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