Umetani K, Tamura K, Komori S, Watanabe A, Ishihara T, Mochizuki S, Li B, Ijiri H
Second Department of Internal Medicine, Yamanashi Medical University, Japan.
Jpn Circ J. 1996 Jun;60(6):349-54. doi: 10.1253/jcj.60.349.
The purpose of this study was to determine whether thromboxane A2 (TXA2) is involved in the development of ventricular arrhythmias produced by coronary artery occlusion. Ventricular arrhythmias were induced by coronary artery occlusion in 66 male Sprague-Dawley rats. Rats were separated into 4 groups, and saline (n = 19) or CV4151 (a TXA2 synthetase inhibitor)(10 mg/kg, n = 14; 30 mg/kg, n = 15; or 100 mg/kg, n = 18) was injected intravenously 5 min before coronary artery occlusion. The antiarrhythmic effect of CV4151 was assessed in terms of the number of ventricular premature complexes (VPCs), the combined duration of ventricular tachycardia (VT) and ventricular fibrillation (Vf), the incidence of Vf, and the mortality rate within 30 min after occlusion. The total number of VPCs was as follows; control: 1789 +/- 330 beats: 10 mg/kg group: 1289 +/- 302 beats: 30 mg/kg group: 1008 +/- 229 beats: 100 mg/kg group: 986 +/- 275 beats, with no significant differences between groups. The incidence of Vf was significantly reduced in the 30 mg/kg and 100 mg/kg groups, as was the combined duration of VT and Vf and the mortality rate. Our results indicate that the TXA2 synthetase inhibitor CV4151 reduces the incidence of lethal arrhythmias induced by coronary artery occlusion in rats.
本研究的目的是确定血栓素A2(TXA2)是否参与冠状动脉闭塞所致室性心律失常的发生。在66只雄性Sprague-Dawley大鼠中通过冠状动脉闭塞诱发室性心律失常。将大鼠分为4组,在冠状动脉闭塞前5分钟静脉注射生理盐水(n = 19)或CV4151(一种TXA2合成酶抑制剂)(10 mg/kg,n = 14;30 mg/kg,n = 15;或100 mg/kg,n = 18)。根据室性早搏(VPC)的数量、室性心动过速(VT)和心室颤动(Vf)的总持续时间、Vf的发生率以及闭塞后30分钟内的死亡率来评估CV4151的抗心律失常作用。VPC的总数如下:对照组:1789±330次搏动;10 mg/kg组:1289±302次搏动;30 mg/kg组:1008±229次搏动;100 mg/kg组:986±275次搏动,各组之间无显著差异。30 mg/kg和100 mg/kg组的Vf发生率、VT和Vf的总持续时间以及死亡率均显著降低。我们的结果表明,TXA2合成酶抑制剂CV4151可降低大鼠冠状动脉闭塞所致致死性心律失常的发生率。