Department of Applied and Experimental Medicine, Chair of Cardiology University of Brescia, Brescia, Italy.
J Cardiovasc Pharmacol Ther. 2012 Dec;17(4):353-6. doi: 10.1177/1074248412442000. Epub 2012 Apr 6.
Ranolazine is an antianginal drug that inhibits a number of ion currents that are important for the genesis of transmembrane cardiac action potential. It was initially developed as an antianginal agent but was found to additionally exert antiarrhythmic actions, due to its multichannel-blocking properties. In recent years, several studies about the antiarrhythmic properties of ranolazine were conducted, demonstrating the beneficial effects of this drug in both atrial and ventricular arrhythmias, such as atrial fibrillation, ventricular premature beats, ventricular tachycardia, torsades de pointes, and ventricular fibrillation. Our aim is to briefly review the main points of these studies, most more experimental than clinical.
雷诺嗪是一种抗心绞痛药物,可抑制对跨膜心肌动作电位发生很重要的多种离子电流。它最初是作为一种抗心绞痛药物开发的,但由于其多通道阻断特性,被发现还具有抗心律失常作用。近年来,进行了多项关于雷诺嗪抗心律失常特性的研究,证明了该药在心房和室性心律失常中的有益作用,如心房颤动、室性早搏、室性心动过速、尖端扭转型室性心动过速和心室颤动。我们的目的是简要回顾这些研究的要点,其中大多数是实验性的而不是临床性的。