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Circulation. 2002;106:1859-1866
Published online before print September 9, 2002, doi: 10.1161/01.CIR.0000031334.49170.FB
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(Circulation. 2002;106:1859.)
© 2002 American Heart Association, Inc.


Basic Science Reports

Two Types of Ventricular Fibrillation in Isolated Rabbit Hearts

Importance of Excitability and Action Potential Duration Restitution

Tsu-Juey Wu, MD; Shien-Fong Lin, PhD; James N. Weiss, MD; Chih-Tai Ting, MD, PhD; Peng-Sheng Chen, MD

From the Division of Cardiology, Department of Medicine, Taichung Veterans General Hospital and Institute of Clinical Medicine, Cardiovascular Research Center, National Yang-Ming University School of Medicine, Taipei, Taiwan (T.-J.W., C.-T.T.); the Division of Cardiology, Department of Medicine, Cedars-Sinai Medical Center, Los Angeles, Calif (S.-F.L., P.-S.C.); and the Division of Cardiology, Department of Medicine, Cardiovascular Research Laboratory (J.N.W.), UCLA School of Medicine, Los Angeles, Calif.

Correspondence to Tsu-Juey Wu, MD, Division of Cardiology, Department of Medicine, Taichung Veterans General Hospital, 160, Section 3, Chung-Kang Road, Taichung, Taiwan. E-mail tjwu{at}vghtc.vghtc.gov.tw

Background— The combined effects of excitability and action potential duration (APD) restitution on wavefront dynamics remain unclear.

Methods and Results— 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 S1 pacing cycle lengths over which CT-1 decreased, converting VT to slow VF.

Conclusions— 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.


Key Words: arrhythmia • fibrillation • mapping • ventricles




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