Naito H, Furukawa Y, Chino D, Yamada C, Hashimoto K
Department of Pharmacology, Yamanashi Medical University, Tamaho-cho, Nakakoma-gun, Yamanashi, 409-3898, Japan.
Eur J Pharmacol. 2000 Jan 28;388(2):171-6. doi: 10.1016/s0014-2999(99)00845-6.
1,3,4,5-Tetrahydro-7,8-dimethoxy-3[3-[[2-(3, 4-dimethoxyphenyl)-ethyl]methylamino]propyl]-2H-3-benzazepin-2-one -hy drochloride (Zatebradine) is a specific bradycardiac agent, blocking the hyperpolarization-activated pacemaker current (I(f)), and thus has no negative inotropic effect. The purpose of this study was to examine whether zatebradine is effective against ischemia and reperfusion-induced arrhythmias in dogs compared to propranolol. Arrhythmia was induced by ligation of the left anterior descending coronary artery followed by reperfusion. Ischemia-induced biphasic arrhythmias were suppressed in both zatebradine and propranolol groups. During ischemia, fatal ventricular fibrillation occurred in four dogs in the control group, 0 in the zatebradine group, and two dogs in the propranolol group. Of the 31 dogs subjected to reperfusion, mortality rates in the zatebradine, propranolol, and control groups were 56%, 75%, and 86%, respectively, and there were no significant differences. In the heart beating 10 beats/min faster than the predrug heart rate by atrial pacing, both zatebradine and propranolol attenuated ischemia-induced arrhythmias but did not affect reperfusion arrhythmias. Our results suggest that I(f) and/or beta-adrenoceptors rather than the bradycardiac action might be related to the antiarrhythmic effects during ischemia, but that they do not play a role in the generation of the reperfusion-induced ventricular arrhythmias.
1,3,4,5-四氢-7,8-二甲氧基-3-[3-[[2-(3,4-二甲氧基苯基)乙基]甲基氨基]丙基]-2H-3-苯并氮杂卓-2-酮盐酸盐(扎替雷定)是一种特异性的减慢心率药物,可阻断超极化激活的起搏电流(I(f)),因此没有负性肌力作用。本研究的目的是检验与普萘洛尔相比,扎替雷定对犬缺血及再灌注诱导的心律失常是否有效。通过结扎左冠状动脉前降支然后再灌注诱导心律失常。扎替雷定组和普萘洛尔组中缺血诱导的双相性心律失常均受到抑制。在缺血期间,对照组有4只犬发生致命性室颤,扎替雷定组为0只,普萘洛尔组为2只。在31只接受再灌注的犬中,扎替雷定组、普萘洛尔组和对照组的死亡率分别为56%、75%和86%,且无显著差异。在通过心房起搏使心率比用药前心率快10次/分钟的心脏中,扎替雷定和普萘洛尔均减轻了缺血诱导的心律失常,但不影响再灌注心律失常。我们的结果表明,I(f)和/或β-肾上腺素能受体而非减慢心率作用可能与缺血期间的抗心律失常作用有关,但它们在再灌注诱导的室性心律失常的发生中不起作用。