Calmodulin Inhibitor W-7 Unmasks a Novel Electrocardiographic Parameter That Predicts Initiation of Torsade de Pointes
- 12 February 2002
- journal article
- other
- Published by Wolters Kluwer Health in Circulation
- Vol. 105 (6) , 770-774
- https://doi.org/10.1161/hc0602.103724
Abstract
Background — We have shown that the calmodulin inhibitor W-7 suppresses torsade de pointes (TdP) without shortening the QT interval, which is consistent with other findings that QT prolongation, per se, is insufficient to generate TdP. ECGs were analyzed from a well-characterized animal model of TdP to identify more reliable predictors of this life-threatening ventricular arrhythmia. Methods and Results — TdP was induced using methoxamine and clofilium in 12 of 14 rabbits pretreated with vehicle control, whereas pretreatment with W-7 (50 μmol/kg), an inhibitor of the intracellular Ca 2+ -binding protein calmodulin, significantly suppressed TdP induction (1 of 11 rabbits with TdP, P Conclusions — Selective suppression of TdP inducibility by W-7, without shortening the duration of cardiac repolarization, allowed identification of the UTA ratio as a new electrocardiographic index for predicting TdP onset. These findings are consistent with the idea that prolonged repolarization is not the proximate cause of arrhythmia initiation, and they suggest that an increased UTA ratio reflects activation of intracellular Ca 2+ /calmodulin–dependent processes that are required for triggering TdP in this model.Keywords
This publication has 23 references indexed in Scilit:
- Measurement and interpretation of QT dispersionProgress in Cardiovascular Diseases, 2000
- QT dispersion as a predictor of long-term mortality in patients with acute myocardial infarction and clinical evidence of heart failureEuropean Heart Journal, 1999
- A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange-Nielsen cardioauditory syndromeNature Genetics, 1997
- A mechanistic link between an inherited and an acquird cardiac arrthytmia: HERG encodes the IKr potassium channelCell, 1995
- A molecular basis for cardiac arrhythmia: HERG mutations cause long QT syndromeCell, 1995
- The Effect of Flunarizine and Ryanodine on Acquired Torsades de Pointes Arrhythmias in the Intact Canine HeartJournal of Cardiovascular Electrophysiology, 1995
- Clinical relevance of cardiac arrhythmias generated by afterdepolarizationsJournal of the American College of Cardiology, 1994
- Proarrhythmic effects of the class III agent almokalant: importance of infusion rate, QT dispersion, and early afterdepolarisationsCardiovascular Research, 1993
- Duration of the QT interval and total and cardiovascular mortality in healthy persons (The Framingham heart study experience)The American Journal of Cardiology, 1991
- QTU-Prolongation and Torsades de Pointes Induced by Putative Class III Antiarrhythmic Agents in the RabbitJournal of Cardiovascular Pharmacology, 1990