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Effect of Ranolazine, an Antianginal Agent With Novel Electrophysiological Properties, on the Incidence of Arrhythmias in Patients With Non–ST-Segment–Elevation Acute Coronary Syndrome
Author(s) -
Benjamin M. Scirica,
David A. Morrow,
Hanoch Hod,
Sabina A. Murphy,
Luiz Belardinelli,
Chester M. Hedgepeth,
Peter Molhoek,
Freek W.A. Verheugt,
Bernard J. Gersh,
Carolyn H. McCabe,
Eugene Braunwald
Publication year - 2007
Publication title -
circulation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 7.795
H-Index - 607
eISSN - 1524-4539
pISSN - 0009-7322
DOI - 10.1161/circulationaha.107.724880
Subject(s) - ranolazine , medicine , cardiology , timi , atrial fibrillation , myocardial infarction , afterdepolarization , acute coronary syndrome , ventricular tachycardia , repolarization , percutaneous coronary intervention , electrophysiology
Ranolazine, a piperazine derivative, reduces ischemia via inhibition of the late phase of the inward sodium current (late I(Na)) during cardiac repolarization, with a consequent reduction in intracellular sodium and calcium overload. Increased intracellular calcium leads to both mechanical dysfunction and electric instability. Ranolazine reduces proarrhythmic substrate and triggers such as early afterdepolarization in experimental models. However, the potential antiarrhythmic actions of ranolazine have yet to be demonstrated in humans.

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