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高血浆浓度普萘洛尔对人体受试者的电生理作用。

Electrophysiologic actions of high plasma concentrations of propranolol in human subjects.

作者信息

Duff H J, Roden D M, Brorson L, Wood A J, Dawson A K, Primm R K, Oates J A, Smith R F, Woosley R L

出版信息

J Am Coll Cardiol. 1983 Dec;2(6):1134-40. doi: 10.1016/s0735-1097(83)80340-4.

Abstract

The authors have previously shown that 40% of patients whose ventricular arrhythmias respond to propranolol require plasma concentrations in excess of those producing substantial beta-receptor blockade (greater than 150 ng/ml). However, the electrophysiologic actions of propranolol have only been examined in human beings after small intravenous doses achieving concentrations of less than 100 ng/ml. In this study, the electrophysiologic effects of a wider concentration range of propranolol was examined in nine patients. Using a series of loading and maintenance infusions, measurements were made at baseline, at low mean plasma propranolol concentrations (104 +/- 17 ng/ml) and at high concentrations (472 +/- 68 ng/ml). Significant (p less than 0.05) increases in AH interval and sinus cycle length were seen at low concentrations of propranolol, with no further prolongation at the high concentrations; these effects are typical of those produced by beta-blockade. However, progressive shortening of the endocardial monophasic action potential duration and QTc interval were seen over the entire concentration range tested (p less than 0.05). At high concentrations, there was significant (p less than 0.05) further shortening of both the QTc and monophasic action potential duration beyond that seen at low propranolol concentrations, along with a progressive increase in the ratio of the ventricular effective refractory period to monophasic action potential duration. No significant changes were seen in HV interval, QRS duration or ventricular effective refractory period. In summary, the concentration-response relations for atrioventricular conductivity and sinus node automaticity were flat above concentrations of 150 ng/ml.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

作者们此前已表明,室性心律失常对普萘洛尔有反应的患者中,40% 需要血浆浓度超过产生显著β受体阻滞作用时的浓度(大于150 ng/ml)。然而,普萘洛尔的电生理作用仅在静脉注射小剂量(达到浓度低于100 ng/ml)后在人体中进行过研究。在本研究中,对9名患者检测了更宽浓度范围的普萘洛尔的电生理效应。通过一系列负荷和维持输注,在基线、低平均血浆普萘洛尔浓度(104±17 ng/ml)和高浓度(472±68 ng/ml)时进行测量。在低浓度普萘洛尔时,AH间期和窦性周期长度显著(p<0.05)增加,高浓度时无进一步延长;这些效应是β受体阻滞典型的效应。然而,在整个测试浓度范围内,心内膜单相动作电位持续时间和QTc间期逐渐缩短(p<0.05)。在高浓度时,QTc和单相动作电位持续时间均显著(p<0.05)进一步缩短,超过低普萘洛尔浓度时所见,同时心室有效不应期与单相动作电位持续时间的比值逐渐增加。HV间期、QRS时限或心室有效不应期未见显著变化。总之,在浓度高于150 ng/ml时,房室传导性和窦房结自律性的浓度 - 反应关系呈平台状。(摘要截选至250字)

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