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酚妥拉明、阿普洛尔和普尼拉明对豚鼠乳头肌动作电位最大上升速率的影响。

Effect of phentolamine, alprenolol and prenylamine on maximum rate of rise of action potential in guinea-pig papillary muscles.

作者信息

Sada H

出版信息

Naunyn Schmiedebergs Arch Pharmacol. 1978 Oct;304(3):191-201. doi: 10.1007/BF00507958.

Abstract

Effects of phentolamine (13.3, 26.5 and 53.0 micron), alprenolol (3.5, 7.0 and 17.5 micron) and prenylamine (2.4, 4.8 and 11.9 micron) on the transmembrane potential were studied in isolated guinea-pig papillary muscles, superfused with Tyrode's solution. 1. Phentolamine, alprenolol and prenylamine reduced the maximum rate of rise of action potential (.Vmax) dose-dependently. Higher concentrations of phentolamine and prenylamine caused a loss of plateau in a majority of the preparations. Resting potential was not altered by any of the drugs. Readmittance of drug-free Tyrode's solution reversed these changes induced by 13.3 micron of phentolamine and all conconcentrations of alprenolol almost completely but those induced by higher concentrations of phentolamine and all concentrations of prenylamine only slightly. 2. .Vmax at steady state was increased with decreasing driving frequencies (0.5 and 0.25 Hz) and was decreased with increasing ones (2--5 Hz) in comparison with that at 1 Hz. Such changes were all exaggerated by the above drugs, particularly by prenylamine. 3. Prenylamine and, to a lesser degree, phentolamine and alprenolol delayed dose-dependently the recovery process of .Vmax in premature responses. 4. .Vmax in the first response after interruption of stimulation recovered toward the predrug value in the presence of the above three drugs. The time constants of recovery process ranged between 10.5 and 15.0s for phentolamine, between 4.5 and 15.5s for alprenolol. The time constant of the main component was estimated to be approximately 2s for the recovery process with prenylamine. 5. On the basis of the model recently proposed by Hondeghem and Katzung (1977), it is suggested that the drug molecules associate with the open sodium channels and dissociated slowly from the closed channels and that the inactivation parameter in the drug-associated channels is shifted in the hyperpolarizing direction.

摘要

在灌流有台氏液的豚鼠离体乳头肌上,研究了酚妥拉明(13.3、26.5和53.0微米)、阿普洛尔(3.5、7.0和17.5微米)和普尼拉明(2.4、4.8和11.9微米)对跨膜电位的影响。1. 酚妥拉明、阿普洛尔和普尼拉明剂量依赖性地降低动作电位最大上升速率(Vmax)。较高浓度的酚妥拉明和普尼拉明使大多数标本的平台期消失。所有药物均未改变静息电位。重新灌流无药台氏液可使13.3微米酚妥拉明和所有浓度阿普洛尔引起的这些变化几乎完全逆转,但较高浓度酚妥拉明和所有浓度普尼拉明引起的变化仅稍有逆转。2. 与1赫兹时相比,稳态Vmax随驱动频率降低(0.5和0.25赫兹)而升高,随驱动频率升高(2 - 5赫兹)而降低。上述药物均使这些变化加剧,尤其是普尼拉明。3. 普尼拉明以及程度较轻的酚妥拉明和阿普洛尔剂量依赖性地延迟早搏反应中Vmax的恢复过程。4. 在上述三种药物存在时,刺激中断后第一个反应中的Vmax恢复到用药前值。酚妥拉明恢复过程的时间常数在10.5至15.0秒之间,阿普洛尔在4.5至15.5秒之间。普尼拉明恢复过程主要成分的时间常数估计约为2秒。5. 根据Hondeghem和Katzung(1977年)最近提出的模型,提示药物分子与开放的钠通道结合,并从关闭的通道缓慢解离,且药物结合通道中的失活参数向超极化方向移动。

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