Hála O, Németh M, Varró A, Papp J G
Department of Pharmacology, Albert Szent-Györgyi Medical University, Szeged, Hungary.
J Cardiovasc Pharmacol. 1994 Oct;24(4):559-65. doi: 10.1097/00005344-199410000-00006.
We studied the electrophysiologic effects of the antiarrhythmic compound detajmium (Tachmalcor) on isolated dog and rabbit cardiac preparations, applying the conventional intracellular microelectrode techniques. In dog ventricular muscle fibers (37 degrees C, stimulation frequency 1 Hz), 1 microM detajmium did not change resting potential (RP), action potential amplitude (APA), AP duration measured at 90% of repolarization (APD90), or effective refractory period (ERP) significantly, but reduced maximum rate of depolarization (Vmax) significantly from 236.7 +/- 28.9 to 177.3 +/- 22.5 V/s (n = 6, p < 0.01). In dog Purkinje fibers (37 degrees C, stimulation frequency 1 Hz), 1 microM detajmium significantly decreased APA from 111.1 +/- 12.3 to 100.0 +/- 2.5 mV (n = 8, p < 0.003), APD90 from 359.0 +/- 17.5 to 262.1 +/- 12.3 ms (n = 8, p < 0.001) and Vmax from 687.5 +/- 57.2 to 523.7 +/- 58.2 V/s (n = 8, p < 0.001) without changing maximal diastolic potential or ERP/APD ratio significantly. The effect of detajmium on Vmax in both dog ventricular muscle and Purkinje fibers was frequency dependent. Fractional Vmax block was 0.185 +/- 0.008 1/AP. The recovery kinetics of Vmax (offset kinetics) was extremely slow (time constant = 348.16 +/- 57.43 s) considerably slower than most of those of other antiarrhythmic drugs yet reported. Detajmium in concentration < 32 microM did not influence the beta-adrenoceptors or slow response APs in dog ventricular tissue significantly. On the basis of its electrophysiologic effects, detajmium, like prajmaline, encainide, or flecainide, can be best classified as a class I/C antiarrhythmic drug according to the Vaughan Williams' classification scheme.
我们采用传统的细胞内微电极技术,研究了抗心律失常化合物德他米姆(Tachmalcor)对离体犬和兔心脏标本的电生理作用。在犬心室肌纤维(37℃,刺激频率1Hz)中,1μM德他米姆对静息电位(RP)、动作电位幅度(APA)、复极化90%时测量的动作电位时程(APD90)或有效不应期(ERP)无显著影响,但最大去极化速率(Vmax)从236.7±28.9显著降低至177.3±22.5V/s(n = 6,p < 0.01)。在犬浦肯野纤维(37℃,刺激频率1Hz)中,1μM德他米姆使APA从111.1±12.3显著降低至100.0±2.5mV(n = 8,p < 0.003),APD90从359.0±17.5显著降低至262.1±12.3ms(n = 8,p < 0.001),Vmax从687.5±57.2显著降低至523.7±58.2V/s(n = 8,p < 0.001),而最大舒张电位或ERP/APD比值无显著变化。德他米姆对犬心室肌和浦肯野纤维Vmax的影响具有频率依赖性。Vmax的分数阻滞为0.185±0.008 1/AP。Vmax的恢复动力学(抵消动力学)极其缓慢(时间常数 = 348.16±57.43s),比迄今报道的大多数其他抗心律失常药物的恢复动力学慢得多。浓度<32μM的德他米姆对犬心室组织中的β - 肾上腺素能受体或慢反应动作电位无显著影响。根据其电生理作用,按照Vaughan Williams分类方案,德他米姆与普拉马林、恩卡胺或氟卡胺一样,最好归类为I/C类抗心律失常药物。