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氟哌利多对不同心脏组织的电生理效应。

Electrophysiological effects of droperidol in different cardiac tissues.

作者信息

Carmeliet E, Xhonneux R, Van Glabbeek A, Reneman R

出版信息

Naunyn Schmiedebergs Arch Pharmacol. 1976;293(1):57-66. doi: 10.1007/BF00498871.

DOI:10.1007/BF00498871
PMID:948352
Abstract

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.

摘要

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。

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本文引用的文献

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A STUDY OF SOME OF THE PHARMACOLOGIC ACTIONS OF DROPERIDOL.氟哌利多的某些药理作用研究。
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ELECTROPHYSIOLOGIC ANTAGONISM AND SYNERGISM OF POTASSIUM AND ANTIARRHYTHMIC AGENTS.钾与抗心律失常药物的电生理拮抗作用和协同作用
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Decreased K+ conductance produced by Ba++ in frog sartorius fibers.钡离子(Ba++)降低青蛙缝匠肌纤维的钾离子(K+)电导。
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Measurement of anti-arrhythmic potency of drugs in man: effects of dehydrobenzperidol.人体中药物抗心律失常效力的测定:脱氢苯哌利多的作用
Anesthesiology. 1967 Mar-Apr;28(2):318-23. doi: 10.1097/00000542-196703000-00005.
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The kinetics and rectifier properties of the slow potassium current in cardiac Purkinje fibres.心脏浦肯野纤维中缓慢钾电流的动力学和整流特性。
J Physiol. 1968 Mar;195(1):185-214. doi: 10.1113/jphysiol.1968.sp008454.
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[On antiarrhythmic properties of certain drugs used as anesthetics (experimental research in dogs). I. Dehydrobenzoperidol].[关于某些用作麻醉剂的药物的抗心律失常特性(犬类实验研究)。I. 脱氢苯哌利多]
Acta Anaesthesiol. 1967 Sep-Oct;18(5):601-7.
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[The anti-arrhythmic action of dehydrobenzperidol].[脱氢苯哌利多的抗心律失常作用]
Minerva Anestesiol. 1970 Apr;36(4):282-5.
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Droperidol in the management of acute circulatory failure.氟哌利多用于急性循环衰竭的治疗。
Arzneimittelforschung. 1970 May;20(5):674-6.
9
Decrease in K+ conductance and depolarization of frog cardiac muscle produced by Ba++.钡离子(Ba++)引起青蛙心肌钾离子(K+)电导降低和去极化。
Am J Physiol. 1970 Oct;219(4):1108-14. doi: 10.1152/ajplegacy.1970.219.4.1108.
10
Two components of the cardiac action potential. I. Voltage-time course and the effect of acetylcholine on atrial and nodal cells of the rabbit heart.心脏动作电位的两个组成部分。I. 电压-时间过程以及乙酰胆碱对兔心脏心房和节点细胞的影响。
J Gen Physiol. 1969 Nov;54(5):607-35. doi: 10.1085/jgp.54.5.607.