ranolazine is an antiischemic agent with novel mechanisms of action to decrease anginal frequency and to improve exercise capacity in patients with chronic stable angina.
basis for the improvement in myocardial ischemia appears to be inhibition of the late phase of the inward sodium current (INa) with consequent attenuation of intracellular calcium overload
at therapeutic concentrations, ranolazine also affects the delayed rectifier potassium current (IKr), which prolongs ventricular action potential duration (APD)
clinically, it has been observed in ambulatory ECG recordings from the MERLIN-TIMI 36 trial that ranolazine exerts significant antiarrhythmic effects, as evidenced by significantly fewer episodes of ventricular tachycardia
net effect in patients with chronic stable angina is a dose-related prolongation of the QT interval
therefore, for current clinical use, ranolazine is "contraindicated" in patients with preexisting QT prolongation and in combination with other QT-prolonging drugs due to concerns about possible proarrhythmias
shortening of action potential duration (and, possibly, antiarrhythmic effect) might be expected under conditions characterized by an abnormal increase in late INa: acute ischemia, some forms of long-QT syndrome type 3 (LQT3), and heart failure
2. Scirica BM, Morrow DA, Hod H, Murphy SA, Belardinelli L, Hedgepeth CM, Molhoek P, Verheugt FW, Gersh BJ, McCabe CH, Braunwald E: 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: Results from the Metabolic Efficiency with Ranolazine for Less Ischemia in Non ST-Elevation Acute Coronary Syndrome Thrombolysis in Myocardial Infarction 36 (MERLIN-TIMI 36) randomized controlled trial. Circulation 2007;116:1647-1652.
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