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起搏器选择性:离子环境及阿利尼定(一种可能的阴离子拮抗剂)对兔心房的影响

Pacemaker selectivity: influence on rabbit atria of ionic environment and of alinidine, a possible anion antagonist.

作者信息

Millar J S, Williams E M

出版信息

Cardiovasc Res. 1981 Jun;15(6):335-50. doi: 10.1093/cvr/15.6.335.

Abstract

Alinidine, a new compound which reduces heart rate in man and animals, has a selective action on the sinus node. The dose-response relation between alinidine and frequency is not altered by atropine, and alinidine does not block the positive chronotropic action of isoprenaline. Alinidine has no negative inotropic action and has no effect on the linear relation between extracellular Ca and force of myocardial contraction. Alinidine did not alter the slope of the relation between frequency and external calcium concentration. Intracellular recordings showed that alinidine had no effect on the maximum rate of depolarisation or overshoot potential of rabbit atrial muscle, nor was conduction velocity, electrical threshold or maximum follow frequency affected. It was concluded that alinidine did not restrict current through fast inward channels. Alinidine did not increase resting potential or accelerate repolarisation, suggesting that potassium conductance was not increased. The effect of alinidine on frequency was not increased in 14 mmol . litre-1 KCl, or decreased in 2.24 mmol . litre-1 KCl, suggesting that the attachment of alinidine to receptors was not voltage-dependent. Spontaneous frequency was higher when NaCl was replaced by NaBr, and the bradycardic effect of alinidine was increased. Conversely, frequency was lower in NaCH3SO4 and the slope of the dose-response curve decreased. Intracellular recordings from sinus node cells showed that alinidine decreased the slope of the slow diastolic depolarisation and increased action potential duration, without altering the overshoot, the maximum diastolic potential, or the "take-off" potential. A possible explanation for these results is that alinidine restricts current through anion-selective channels. If so, the high potency of alinidine suggests that anionic current normally carries a substantial fraction of the current causing slow diastolic depolarisation.

摘要

阿利尼定是一种能降低人和动物心率的新化合物,对窦房结有选择性作用。阿利尼定与频率之间的剂量 - 反应关系不受阿托品影响,且阿利尼定不阻断异丙肾上腺素的正性变时作用。阿利尼定无负性肌力作用,对细胞外钙与心肌收缩力之间的线性关系也无影响。阿利尼定未改变频率与细胞外钙浓度之间关系的斜率。细胞内记录显示,阿利尼定对兔心房肌的最大去极化速率或超射电位无影响,传导速度、电阈值或最大跟随频率也未受影响。得出的结论是,阿利尼定不限制通过快速内向通道的电流。阿利尼定未增加静息电位或加速复极化,提示钾电导未增加。在14 mmol·L⁻¹ KCl中,阿利尼定对频率的作用未增强,在2.24 mmol·L⁻¹ KCl中也未减弱,提示阿利尼定与受体的结合不依赖电压。当NaCl被NaBr取代时,自发频率更高,且阿利尼定的减慢心率作用增强。相反,在NaCH₃SO₄中频率更低,剂量 - 反应曲线的斜率减小。窦房结细胞的细胞内记录显示,阿利尼定降低了缓慢舒张期去极化的斜率并增加了动作电位持续时间,而未改变超射、最大舒张电位或“起始”电位。对这些结果的一种可能解释是,阿利尼定限制通过阴离子选择性通道的电流。如果是这样,阿利尼定的高效能表明阴离子电流通常携带导致缓慢舒张期去极化的大部分电流。

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