Carmeliet E, Xhonneux R, Van Glabbeek A, Reneman R
Naunyn Schmiedebergs Arch Pharmacol. 1976;293(1):57-66. doi: 10.1007/BF00498871.
The effect of droperidol in concentrations between 0.05 and 5 mg/I was evaluated on different electrophysiological variables in auricular preparations of the guinea-pig, papillary muscles of dog and cat, Purkinje fibres of the dog, cow and sheep. At low concentration (0.25 to 0.5mg/I) droperidol decreased pacemaker activity and prolonged the effective refractroy period. The inhibition of pacemaker activity was not accompanied by a reduction in the rate of early diastolic depolarization, but was related to an inhibition of the depolarization process during late diastole. At high concentrations (5mg/I) resting potential, action potential amplitude, (dV/dt)max and conduction velocity were reduced. Reduction of dV/dt during the upstroke was more pronounced at lower membrane potentials, the inactivation curve was shifted to more negative membrane potentials. The action potential was lengthened or shortened, the effect being dependent on the frequency, dose, exposure time and animal species. Droperidol had no deleterious effect on Ca-mediated action potentials. The antiarrhythmic activity of droperidol in therapeutic concentrations (0.25 and 0.5mg/I) can be explained by the reduction of pacemaker activity and the lengthening of the effective refractory period. In terms of changes in ion conductance most effects can be explained by a reduction in Na conductance. No simple explanation can be offered for the complex changes in action potential duration.
在豚鼠耳廓标本、犬和猫的乳头肌、犬、牛和羊的浦肯野纤维中,评估了浓度在0.05至5mg/I之间的氟哌利多对不同电生理变量的影响。在低浓度(0.25至0.5mg/I)时,氟哌利多可降低起搏活动并延长有效不应期。对起搏活动的抑制并不伴有舒张早期去极化速率的降低,而是与舒张晚期去极化过程的抑制有关。在高浓度(5mg/I)时,静息电位、动作电位幅度、(dV/dt)max和传导速度降低。在较低膜电位时,上升期dV/dt的降低更为明显,失活曲线向更负的膜电位移动。动作电位延长或缩短,其效果取决于频率、剂量、暴露时间和动物种类。氟哌利多对钙介导的动作电位无有害影响。氟哌利多在治疗浓度(0.25和0.5mg/I)时的抗心律失常活性可通过起搏活动的降低和有效不应期的延长来解释。就离子电导的变化而言,大多数效应可通过钠电导的降低来解释。对于动作电位持续时间的复杂变化,无法给出简单的解释。