Ranolazine, an antianginal agent, markedly reduces ventricular arrhythmias induced by ischemia and ischemia-reperfusion

被引:63
作者
Dhalla, Arvinder K. [1 ]
Wang, Wei-Qun
Dow, Joan [2 ]
Shryock, John C.
Belardinelli, Luiz
Bhandari, Anil [2 ]
Kloner, Robert A. [2 ,3 ]
机构
[1] CV Therapeut Inc, Dept Pharmacol, Palo Alto, CA 94304 USA
[2] Hosp Good Samaritan, Inst Heart, Los Angeles, CA 90017 USA
[3] Univ So Calif, Keck Sch Med, Los Angeles, CA 90033 USA
来源
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY | 2009年 / 297卷 / 05期
关键词
arrhythmias; ranolazine; myocardial ischemia-reperfusion; ventricular tachycardia; ventricular fibrillation; LATE SODIUM CURRENT; HYDROGEN-PEROXIDE; CONTROLLED-TRIAL; ANGINA-PECTORIS; CHANNEL; RAT; ISCHEMIA/REPERFUSION; PATHOPHYSIOLOGY; DYSFUNCTION; INHIBITOR;
D O I
10.1152/ajpheart.00173.2009
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Dhalla AK, Wang WQ, Dow J, Shryock JC, Belardinelli L, Bhandari A, Kloner RA. Ranolazine, an antianginal agent, markedly reduces ventricular arrhythmias induced by ischemia and ischemia-reperfusion. Am J Physiol Heart Circ Physiol 297: H1923-H1929, 2009. First published September 18, 2009; doi:10.1152/ajpheart.00173.2009.-We tested the effect of the antianginal agent ranolazine on ventricular arrhythmias in an ischemic model using two protocols. In protocol 1, anesthetized rats received either vehicle or ranolazine (10 mg/kg, iv bolus) and were subjected to 5 min of left coronary artery (LCA) occlusion and 5 min of reperfusion with electrocardiogram and blood pressure monitoring. In protocol 2, rats received either vehicle or three doses of ranolazine (iv bolus followed by infusion) and 20 min of LCA occlusion. With protocol 1, ventricular tachycardia (VT) occurred in 9/12 (75%) vehicle-treated rats and 1/11 (9%) ranolazine-treated rats during reperfusion (P = 0.003). Sustained VT occurred in 5/12 (42%) vehicle-treated but 0/11 in ranolazine-treated rats (P = 0.037). The median number of episodes of VT during reperfusion in vehicle and ranolazine groups was 5.5 and 0, respectively (P = 0.0006); median duration of VT was 22.2 and 0 s in vehicle and ranolazine rats, respectively (P = 0.0006). With protocol 2, mortality in the vehicle group was 42 vs. 17% (P = 0.371), 10% (P = 0.162) and 0% (P = 0.0373) with ranolazine at plasma concentrations of 2, 4, and 8 mu M, respectively. Ranolazine significantly reduced the incidence of ventricular fibrillation [67% in controls vs. 42% (P = 0.414), 30% (P = 0.198) and 8% (P = 0.0094) in ranolazine at 2, 4, and 8 mu M, respectively]. Median number (2.5 vs. 0; P = 0.0431) of sustained VT episodes, incidence of sustained VT (83 vs. 33%, P = 0.0361), and the duration of VT per animal (159 vs. 19 s; P = 0.0410) were also significantly reduced by ranolazine at 8 mu M. Ranolazine markedly reduced ischemia-reperfusion induced ventricular arrhythmias. Ranolazine demonstrated promising anti-arrhythmic properties that warrant further investigation.
引用
收藏
页码:H1923 / H1929
页数:7
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