Screening for Acute I-Kr Block Is Insufficient to Detect Torsades de Pointes Liability Role of Late Sodium Current

Article

关键词: LONG QT SYNDROME;    REDUCED REPOLARIZATION RESERVE;    CELL-DERIVED CARDIOMYOCYTES;    RECTIFIER POTASSIUM CURRENT;    INTERVAL PROLONGATION;    VENTRICULAR MYOCYTES;    LENGTHENS REPOLARIZATION;    CARDIAC REPOLARIZATION;    ATRIAL-FIBRILLATION;    CURRENT CONTRIBUTES;   

DOI  :  10.1161/CIRCULATIONAHA.113.007765

来源: SCIE

【 摘 要 】

Background-New drugs are routinely screened for I-Kr blocking properties thought to predict QT prolonging and arrhythmogenic liability. However, recent data suggest that chronic (hours) drug exposure to phosphoinositide 3-kinase inhibitors used in cancer can prolong QT by inhibiting potassium currents and increasing late sodium current (INa-L) in cardiomyocytes. We tested the extent to which I-Kr blockers with known QT liability generate arrhythmias through this pathway. Methods and Results-Acute exposure to dofetilide, an I-Kr blocker without other recognized electropharmacologic actions, produced no change in ion currents or action potentials in adult mouse cardiomyocytes, which lack I-Kr. By contrast, 2 to 48 hours of exposure to the drug generated arrhythmogenic afterdepolarizations and >= 15-fold increases in INa-L. Including phosphatidylinositol 3,4,5-trisphosphate, a downstream effector for the phosphoinositide 3-kinase pathway, in the pipette inhibited these effects. INa-L was also increased, and inhibitable by phosphatidylinositol 3,4,5-trisphosphate, with hours of dofetilide exposure in human-induced pluripotent stem cell-derived cardiomyocytes and in Chinese hamster ovary cells transfected with SCN5A, encoding sodium current. Cardiomyocytes from dofetilide-treated mice similarly demonstrated increased INa-L and afterdepolarizations. Other agents with variable I-Kr -blocking potencies and arrhythmia liability produced a range of effects on INa-L, from marked increases (E-4031, d-sotalol, thioridazine, and erythromycin) to little or no effect (haloperidol, moxifloxacin, and verapamil). Conclusions-Some but not all drugs designated as arrhythmogenic I-Kr blockers can generate arrhythmias by augmenting INa-L through the phosphoinositide 3-kinase pathway. These data identify a potential mechanism for individual susceptibility to proarrhythmia and highlight the need for a new paradigm to screen drugs for QT prolonging and arrhythmogenic liability.

【 授权许可】

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