Calmodulin inhibitor W-7 unmasks a novel electrocardiographic parameter that predicts initiation of Torsade de Pointes

Article

关键词: LONG QT SYNDROME;    DE-POINTES;    HEART-FAILURE;    CARDIOVASCULAR MORTALITY;    VENTRICULAR-TACHYCARDIA;    MYOCARDIAL-INFARCTION;    CARDIAC-ARRHYTHMIA;    POTASSIUM CHANNEL;    LOOP MORPHOLOGY;    PROTEIN-KINASE;   

DOI  :  10.1161/hc0602.103724

来源: SCIE

【 摘 要 】

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 TO 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 mumol/kg), an inhibitor of the intracellular Ca2+-binding protein calmodulin, significantly suppressed TdP induction (1 of 11 rabbits with UP. P<0.001). W-7 did not affect heart rate, increases in QT intervals, or dispersion compared with measurements in vehicle-treated control animals. However, a progressive and significant increase in the ratio of U-wave to T-wave amplitude (UTA) occurred before TdP onset in control animals, and this was prevented by W-7. Conclusions-Selective suppression of UP inducibility by W-7, without shortening the duration of cardiac repolarization, allowed identification of the UTA ratio as a new electrocardiographic index for predicting TO 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 Ca2+/calmodulin-dependent processes that are required for triggering UP in this model.

【 授权许可】

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