Two types of ventricular fibrillation in isolated rabbit hearts: Importance of excitability and action potential duration restitution

The combined effects of excitability and action potential duration (APD) restitution on wavefront dynamics remain unclear. We used optical mapping techniques to study Langendorff-perfused rabbit hearts. In protocol IA (n=10), D600 at increasing concentrations was infused during ventricular fibrillat...

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Veröffentlicht in:Circulation (New York, N.Y.) N.Y.), 2002-10, Vol.106 (14), p.1859-1866
Hauptverfasser: WU, Tsu-Juey, LIN, Shien-Fong, WEISS, James N, TING, Chih-Tai, CHEN, Peng-Sheng
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container_issue 14
container_start_page 1859
container_title Circulation (New York, N.Y.)
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creator WU, Tsu-Juey
LIN, Shien-Fong
WEISS, James N
TING, Chih-Tai
CHEN, Peng-Sheng
description The combined effects of excitability and action potential duration (APD) restitution on wavefront dynamics remain unclear. We used optical mapping techniques to study Langendorff-perfused rabbit hearts. In protocol IA (n=10), D600 at increasing concentrations was infused during ventricular fibrillation (VF). With concentration increased to 0.5 mg/L, fast VF (dominant frequency, 19.1+/-1.8 Hz) was consistently converted to ventricular tachycardia (VT). However, increasing D600 further to 2.5 or 5.0 mg/L converted VT to slow VF (11.9+/-2.3 Hz, P=0.0011). In an additional 4 hearts (protocol IB), tetrodotoxin converted a preexisting VT to slow VF (11.0+/-1.4 Hz). Optical maps show wandering wavelets in fast VF, organized reentry in VT, and spatiotemporal periodicity in slow VF. In protocol II, we determined APD and conduction time(-1) (CT(-1)) restitutions during D600 infusion. CT(-1) was used as an estimate of excitability. At 0.1 mg/L, APD and CT(-1) restitutions were steep and flat, respectively. APD restitution became flattened when D600 increased to 0.5 mg/L, converting fast VF to VT. Further increasing D600 to 2.5 or 5.0 mg/L steepened CT(-1) restitution and widened the range of S(1) pacing cycle lengths over which CT(-1) decreased, converting VT to slow VF. Two types of VF exist in isolated rabbit hearts. Fast (type I) VF is associated with a steep APD restitution, a flat CT(-1) restitution, and wandering wavelets. Slow (type II) VF is associated with a flat APD restitution, a steep CT(-1) restitution, and spatiotemporal periodicity. Both excitability and APD restitution are important in VF maintenance.
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We used optical mapping techniques to study Langendorff-perfused rabbit hearts. In protocol IA (n=10), D600 at increasing concentrations was infused during ventricular fibrillation (VF). With concentration increased to 0.5 mg/L, fast VF (dominant frequency, 19.1+/-1.8 Hz) was consistently converted to ventricular tachycardia (VT). However, increasing D600 further to 2.5 or 5.0 mg/L converted VT to slow VF (11.9+/-2.3 Hz, P=0.0011). In an additional 4 hearts (protocol IB), tetrodotoxin converted a preexisting VT to slow VF (11.0+/-1.4 Hz). Optical maps show wandering wavelets in fast VF, organized reentry in VT, and spatiotemporal periodicity in slow VF. In protocol II, we determined APD and conduction time(-1) (CT(-1)) restitutions during D600 infusion. CT(-1) was used as an estimate of excitability. At 0.1 mg/L, APD and CT(-1) restitutions were steep and flat, respectively. APD restitution became flattened when D600 increased to 0.5 mg/L, converting fast VF to VT. Further increasing D600 to 2.5 or 5.0 mg/L steepened CT(-1) restitution and widened the range of S(1) pacing cycle lengths over which CT(-1) decreased, converting VT to slow VF. Two types of VF exist in isolated rabbit hearts. Fast (type I) VF is associated with a steep APD restitution, a flat CT(-1) restitution, and wandering wavelets. Slow (type II) VF is associated with a flat APD restitution, a steep CT(-1) restitution, and spatiotemporal periodicity. 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Vascular system ; Dose-Response Relationship, Drug ; Electrocardiography - drug effects ; Electrocardiography - methods ; Electrodes, Implanted ; Electrophysiologic Techniques, Cardiac ; Fluorescent Dyes ; Fourier Analysis ; Gallopamil - pharmacology ; Heart ; Heart - drug effects ; Heart - physiopathology ; In Vitro Techniques ; Light ; Medical sciences ; Optics and Photonics ; Pyridinium Compounds ; Rabbits ; Sodium Channel Blockers - pharmacology ; Tachycardia, Ventricular - drug therapy ; Tachycardia, Ventricular - physiopathology ; Tetrodotoxin - pharmacology ; Time Factors ; Ventricular Fibrillation - classification ; Ventricular Fibrillation - drug therapy ; Ventricular Fibrillation - physiopathology</subject><ispartof>Circulation (New York, N.Y.), 2002-10, Vol.106 (14), p.1859-1866</ispartof><rights>2002 INIST-CNRS</rights><rights>Copyright American Heart Association, Inc. 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We used optical mapping techniques to study Langendorff-perfused rabbit hearts. In protocol IA (n=10), D600 at increasing concentrations was infused during ventricular fibrillation (VF). With concentration increased to 0.5 mg/L, fast VF (dominant frequency, 19.1+/-1.8 Hz) was consistently converted to ventricular tachycardia (VT). However, increasing D600 further to 2.5 or 5.0 mg/L converted VT to slow VF (11.9+/-2.3 Hz, P=0.0011). In an additional 4 hearts (protocol IB), tetrodotoxin converted a preexisting VT to slow VF (11.0+/-1.4 Hz). Optical maps show wandering wavelets in fast VF, organized reentry in VT, and spatiotemporal periodicity in slow VF. In protocol II, we determined APD and conduction time(-1) (CT(-1)) restitutions during D600 infusion. CT(-1) was used as an estimate of excitability. At 0.1 mg/L, APD and CT(-1) restitutions were steep and flat, respectively. APD restitution became flattened when D600 increased to 0.5 mg/L, converting fast VF to VT. Further increasing D600 to 2.5 or 5.0 mg/L steepened CT(-1) restitution and widened the range of S(1) pacing cycle lengths over which CT(-1) decreased, converting VT to slow VF. Two types of VF exist in isolated rabbit hearts. Fast (type I) VF is associated with a steep APD restitution, a flat CT(-1) restitution, and wandering wavelets. Slow (type II) VF is associated with a flat APD restitution, a steep CT(-1) restitution, and spatiotemporal periodicity. Both excitability and APD restitution are important in VF maintenance.</abstract><cop>Hagerstown, MD</cop><pub>Lippincott Williams &amp; Wilkins</pub><pmid>12356642</pmid><doi>10.1161/01.CIR.0000031334.49170.FB</doi><tpages>8</tpages></addata></record>
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source MEDLINE; American Heart Association Journals; EZB-FREE-00999 freely available EZB journals; Journals@Ovid Complete
subjects Action Potentials - drug effects
Action Potentials - physiology
Animals
Biological and medical sciences
Body Surface Potential Mapping
Calcium Channel Blockers - pharmacology
Cardiac dysrhythmias
Cardiac Pacing, Artificial
Cardiology. Vascular system
Dose-Response Relationship, Drug
Electrocardiography - drug effects
Electrocardiography - methods
Electrodes, Implanted
Electrophysiologic Techniques, Cardiac
Fluorescent Dyes
Fourier Analysis
Gallopamil - pharmacology
Heart
Heart - drug effects
Heart - physiopathology
In Vitro Techniques
Light
Medical sciences
Optics and Photonics
Pyridinium Compounds
Rabbits
Sodium Channel Blockers - pharmacology
Tachycardia, Ventricular - drug therapy
Tachycardia, Ventricular - physiopathology
Tetrodotoxin - pharmacology
Time Factors
Ventricular Fibrillation - classification
Ventricular Fibrillation - drug therapy
Ventricular Fibrillation - physiopathology
title Two types of ventricular fibrillation in isolated rabbit hearts: Importance of excitability and action potential duration restitution
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