Cimini M G, Brunden M N, Gibson J K
Cardiovascular Diseases Research, Upjohn Company, Kalamazoo, MI 49001.
Eur J Pharmacol. 1992 Nov 3;222(1):93-8. doi: 10.1016/0014-2999(92)90467-i.
Ibutilide fumarate is currently in Phase II clinical trials for the treatment of life-threatening cardiac arrhythmias. The cardiovascular effects of ibutilide and its d- and l-stereoisomers, U82208E and U82209E were tested in an isolated rabbit myocardium system. In a series of repeated measures experiments, threshold, effective refractory period, force of contraction, conduction time and rate were measured at various pacing frequencies in isolated papillary muscles, ventricular muscle strips and right atria exposed to 10(-7), 10(-6) and 10(-5) M drug. Although there were occasional instances where one form had a greater or lesser effect on a given parameter, overall there was little pharmacological difference between the racemic mixture and its constituent forms. At the highest dose, effective refractory periods at 1 and 3 Hz increased by 18-32 ms, conduction times measured at 3 Hz increased by 27-30% and atrial rate decreased by 19-32%, while threshold and force of contraction were generally unaffected. In this study there were no clear cut pharmacologic differences between the three forms of this class III antiarrhythmic agent. Parallel studies to determine pA2 values of ibutilide and sotalol demonstrated that ibutilide possesses weak beta-adrenoceptor blocking properties.
富马酸伊布利特目前正处于治疗危及生命的心律失常的II期临床试验阶段。在离体兔心肌系统中测试了伊布利特及其d-和l-立体异构体U82208E和U82209E的心血管效应。在一系列重复测量实验中,在暴露于10(-7)、10(-6)和10(-5) M药物的离体乳头肌、心室肌条和右心房中,于不同起搏频率下测量阈值、有效不应期、收缩力、传导时间和心率。尽管偶尔会出现一种形式对某一特定参数的影响较大或较小的情况,但总体而言,外消旋混合物与其组成形式之间在药理学上几乎没有差异。在最高剂量下,1 Hz和3 Hz时的有效不应期增加18 - 32 ms,3 Hz时测量的传导时间增加27 - 30%,心房率降低19 - 32%,而阈值和收缩力通常未受影响。在本研究中,这种III类抗心律失常药物的三种形式之间没有明显的药理学差异。确定伊布利特和索他洛尔pA2值的平行研究表明,伊布利特具有较弱的β-肾上腺素能受体阻断特性。