Spence S G, Vetter C, Hoe C M
Department of Safety Assessment, Merck Research Laboratories, West Point, Pennsylvania 19486.
Teratology. 1994 Apr;49(4):282-92. doi: 10.1002/tera.1420490408.
Gestation day 11 (GD11) and 14 (GD14) embryos were cultured for up to 4 hours in the presence of Dofetilide (0.01-0.50 microgram/ml), a potent Class III Antiarrhythmic which selectively inhibits the rapid component of the time dependent outward potassium current (IKr). Significant (P < or = 0.05) reductions in heart rate (HR) as measured over a 4 hour period were dose dependent and reversible. The sensitivity of the GD11 embryos was greater than GD14 embryos (14-64% decrease in HR vs. an 11-43% decrease in HR, respectively) at the same concentrations tested. These in vitro results support the hypothesis that the embryo-lethality of Class III Antiarrhythmics observed in vivo may be a class effect of the IKr subtype potassium channel blockers. The data suggest a possible mechanism of embryotoxicity is to lower embryonic HR resulting in subsequent hypoxia and death. Dofetilide's effects on GD11 HR were partially reversible by the sequential addition of Isoproterenol or Theophylline.
在存在多非利特(0.01 - 0.50微克/毫升)的情况下,将妊娠第11天(GD11)和第14天(GD14)的胚胎培养长达4小时。多非利特是一种强效III类抗心律失常药物,可选择性抑制时间依赖性外向钾电流(IKr)的快速成分。在4小时期间测量的心率(HR)显著(P≤0.05)降低,呈剂量依赖性且可逆。在相同测试浓度下,GD11胚胎的敏感性高于GD14胚胎(HR分别降低14 - 64%和11 - 43%)。这些体外结果支持以下假设:在体内观察到的III类抗心律失常药物的胚胎致死性可能是IKr亚型钾通道阻滞剂的类效应。数据表明胚胎毒性的一种可能机制是降低胚胎心率,导致随后的缺氧和死亡。通过依次添加异丙肾上腺素或茶碱,多非利特对GD11心率的影响部分可逆。