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一种新型强心药物阿克里林对窦房结及心脏浦肯野纤维当前潜在起搏活动的影响。

The influence of a new cardiotonic drug, acrihellin, on sinus node and the current underlying pacemaker activity of cardiac Purkinje fibres.

作者信息

Ziskoven R, Wiemer J, Achenbach C

出版信息

Arzneimittelforschung. 1983;33(8):1106-13.

PMID:6685487
Abstract

The spontaneous beating frequency of guinea pig sino-atrial preparations was observed under the influence of 3 beta, 5, 14-trihydroxy-19-oxo-5 beta-bufa-20,22-dienolide-3-(3-methylcrotonate (D 12316, acrihellin), a new cardiotonic drug. There was a slight acceleration of spontaneous frequency after administering rather high doses (10(-6) mol/l) of the drug. Voltage clamp experiments were performed in sheep cardiac Purkinje fibres. AcriheLlin strongly affected the current underlying pacemaker activity, ik2. The kinetic parameter s infinity of this current system was shifted in the hyperpolarizing direction by 4-13 mV. The amplitude of the pacemaker current in Purkinje fibres was reduced by up to 25% in voltage clamp experiments, but the reversal potential and the inward going rectification were left unchanged. After exposure to adrenaline (epinephrine) the well-known depolarizing shift of s infinity was partially restored by acrihellin. This can be interpreted as an antiadrenergic effect of the drug similar to that of beta-adrenoceptor antagonists. However, beta-blockers do not affect the pacemaker kinetics of fibres untreated with adrenaline as does acrihellin. This suggests that the interplay of acrihellin and adrenaline is not that of an agonist and antagonist at a membrane receptor but rather the overlapping of two separate membrane effects.

摘要

在新型强心药3β,5,14 - 三羟基 - 19 - 氧代 - 5β - 蟾蜍 - 20,22 - 二烯内酯 - 3 -(3 - 甲基巴豆酸酯)(D 12316,阿克里林)的影响下,观察豚鼠窦房结制剂的自发搏动频率。给予较高剂量(10^(-6) mol/l)的该药物后,自发频率有轻微加快。在绵羊心脏浦肯野纤维上进行了电压钳实验。阿克里林强烈影响起搏点活动的基础电流ik2。该电流系统的动力学参数s无穷大向超极化方向移动了4 - 13 mV。在电压钳实验中,浦肯野纤维中起搏电流的幅度降低了高达25%,但反转电位和内向整流未发生变化。暴露于肾上腺素后,阿克里林部分恢复了s无穷大的去极化偏移。这可以解释为该药物的抗肾上腺素能作用,类似于β - 肾上腺素能受体拮抗剂的作用。然而,β - 阻滞剂不像阿克里林那样影响未用肾上腺素处理的纤维的起搏动力学。这表明阿克里林和肾上腺素之间的相互作用不是膜受体上激动剂与拮抗剂的相互作用,而是两种独立膜效应的重叠。

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