Sugiyama A, Ni C, Arita J, Eto K, Xue Y X, Hashimoto K
Department of Pharmacology, Yamanashi Medical University Tamaho-cho, Japan.
Toxicol Appl Pharmacol. 1996 Jul;139(1):109-14. doi: 10.1006/taap.1996.0148.
The cardiovascular effects of the antihypoxic and neuroprotective drug, lubeluzole, were investigated using beagle dogs anesthetized with halothane. Endocardial-contact electrode catheter was used for continuous monitoring of monophasic action potential (MAP), which could provide a precise information of repolarization phase. Intravenous administration of an efficacious dose of lubeluzole (0.63 mg/kg, n = 6) slightly decreased both the heart rate and the blood pressure. It did not change PQ interval and QRS width, while it significantly prolonged QT interval, corrected QT (QTc) and the duration of the MAP during the observation period over 60 min. The effects of drug on repolarization phase were late-onset and long-lasting compared with the time course of plasma drug concentrations, which changed as predicted by the two-compartment theory of pharmacokinetics. Additional injection of lubeluzole (2.5 mg/kg, n = 6) showed qualitatively similar changes to those of lower dose, and did not induce the cardiovascular collapse in any dog. Neither afterdepolarization nor ventricular escaped beat was detected during the observation period. The drug concentration in cardiac tissue was correlated linearly with the plasma drug concentration at 60 min after the second drug administration. These results indicate that lubeluzole exerts only minor cardiovascular effects except the prolongation of the repolarization period. The monitoring of plasma drug concentration may be helpful to estimate the steady-state distribution of drug to the heart, but less helpful to predict the QT prolongation. In future clinical trials, care must be taken with patients, especially those at risk to have prolonged repolarization.
使用氟烷麻醉的比格犬研究了抗缺氧和神经保护药物鲁贝唑的心血管作用。采用心内膜接触电极导管连续监测单相动作电位(MAP),其可提供复极化阶段的精确信息。静脉注射有效剂量的鲁贝唑(0.63mg/kg,n = 6)可使心率和血压略有下降。它不改变PQ间期和QRS宽度,而在超过60分钟的观察期内,它可显著延长QT间期、校正QT(QTc)和MAP的持续时间。与血浆药物浓度的时间进程相比,药物对复极化阶段的影响起效较晚且持续时间长,血浆药物浓度的变化符合药代动力学的二室理论预测。额外注射鲁贝唑(2.5mg/kg,n = 6)显示出与低剂量时定性相似的变化,且未在任何犬只中诱发心血管衰竭。在观察期内未检测到后去极化或室性逸搏。第二次给药后60分钟时,心脏组织中的药物浓度与血浆药物浓度呈线性相关。这些结果表明,除了延长复极化期外,鲁贝唑仅产生轻微的心血管作用。监测血浆药物浓度可能有助于估计药物在心脏中的稳态分布,但对预测QT延长的帮助较小。在未来的临床试验中,必须对患者,尤其是那些有复极化延长风险的患者加以关注。