Dennis P D, Williams E M
Cardiovasc Res. 1986 May;20(5):375-8. doi: 10.1093/cvr/20.5.375.
Alinidine, the N-allyl derivative of clonidine, reduces heart rate in animals and man by a selective action on the sinoatrial node. In this study, in the presence of caesium, which blocks the time dependent inward current activated by hyperpolarisation (ih or if), alinidine still caused a concentration related bradycardia in the rabbit sinoatrial node. Within the clinical range of concentrations of alinidine the curve relating heart rate to alinidine concentration in the presence of caesium was parallel to that observed in its absence. It is concluded that the alinidine induced bradycardia cannot be attributed to blockade of ih.
阿利尼定是可乐定的N -烯丙基衍生物,通过对窦房结的选择性作用降低动物和人的心率。在本研究中,在存在铯的情况下(铯可阻断由超极化激活的时间依赖性内向电流(ih或if)),阿利尼定仍可在兔窦房结中引起浓度相关的心动过缓。在阿利尼定的临床浓度范围内,存在铯时心率与阿利尼定浓度的曲线与其不存在时观察到的曲线平行。得出的结论是,阿利尼定诱导的心动过缓不能归因于对ih的阻断。