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肼屈嗪的变时效应及其症状性窦性心动过缓的机制。

Chronotropic effect of hydralazine and its mechanism of symptomatic sinus bradycardia.

作者信息

Lewis B S, Rozenman Y, Merdler A, Rodeanu M E, Shefer A, Halon D A

出版信息

Am J Cardiol. 1987 Jan 1;59(1):93-6. doi: 10.1016/s0002-9149(87)80077-2.

Abstract

The positive chronotropic effect of hydralazine was studied in 9 patients with symptomatic sinus bradycardia. Hydralazine was given in an intravenous dose of 0.15 mg/kg and heart rate, blood pressure, sinoatrial conduction time (Narula method) and corrected sinus node recovery time were measured. The effect of hydralazine was also studied after total autonomic nervous system blockade using 0.04 mg/kg of atropine and 0.2 mg/kg of propranolol intravenously. In the control state hydralazine produced an increase of 28 +/- 15% (mean +/- standard deviation) in heart rate, and this was essentially due to a decrease in sinoatrial conduction time (by 32 +/- 32%, p less than 0.05). Corrected sinus node recovery time also tended to shorten (decrease of 21 +/- 34%, difference not significant). After total autonomic blockade intrinsic heart rate did not change or increased very little (9 +/- 14%) after administration of hydralazine and there was no consistent change in sinoatrial conduction and corrected sinus node recovery times. The small residual effect of hydralazine on heart rate was related to incomplete autonomic blockade, since the effect of postural change (standing) on heart rate was also not totally abolished. The study showed that the positive chronotropic effect of hydralazine was mainly due to a change in sinoatrial conduction with a smaller change in corrected sinus node recovery time, and the major chronotropic effect of the drug was mediated by the autonomic nervous system.

摘要

对9例有症状性窦性心动过缓的患者研究了肼屈嗪的正性变时作用。静脉给予肼屈嗪,剂量为0.15mg/kg,测量心率、血压、窦房传导时间(纳鲁拉法)和校正窦房结恢复时间。在静脉注射0.04mg/kg阿托品和0.2mg/kg普萘洛尔进行完全自主神经系统阻滞之后,也研究了肼屈嗪的作用。在对照状态下,肼屈嗪使心率增加28±15%(均值±标准差),这主要是由于窦房传导时间缩短(32±32%,p<0.05)。校正窦房结恢复时间也有缩短趋势(缩短21±34%,差异无统计学意义)。完全自主神经阻滞后,给予肼屈嗪后固有心率未改变或仅有很小增加(9±14%),窦房传导和校正窦房结恢复时间无一致变化。肼屈嗪对心率的微小残余作用与自主神经阻滞不完全有关,因为体位改变(站立)对心率的影响也未完全消除。该研究表明,肼屈嗪的正性变时作用主要是由于窦房传导改变,校正窦房结恢复时间改变较小,且该药的主要变时作用由自主神经系统介导。

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