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在水平灌注的豚鼠心脏中记录单相动作电位。一种研究药物诱导的心脏电生理变化的体外方法。

Recording of monophasic action potentials in the horizontally perfused guinea pig heart. An in vitro method to study drug-induced changes in cardiac electrophysiology.

作者信息

Reid J J, Duker G

机构信息

Department of Pharmacology and Biochemistry, Hässle Cardiovascular Research Laboratories, Mölndal, Sweden.

出版信息

J Pharmacol Methods. 1987 Nov;18(3):205-17. doi: 10.1016/0160-5402(87)90071-4.

Abstract

An in vitro technique has been developed for the recording of monophasic action potentials to enable the measurement of changes in the duration of repolarization and in rise time produced by known concentrations of drugs and ions. Guinea pig hearts were perfused horizontally at constant pressure (60 cm H2O) and temperature (37 degrees C) with Krebs-Henseleit buffer. Epicardial monophasic action potentials were recorded from the right ventricular base using a bipolar Ag/AgCl electrode to which a suction pressure of 400 mm Hg was applied. The monophasic action potential signals had smooth depolarization and repolarization phases with amplitudes of 25-65 mV; repeated measurements of monophasic action potential duration at the 50, 75, and 90% repolarization levels (MAPD 50, 75, and 90) and rise time, determined by computer analysis, were reproducible for at least 150 min of perfusion. There was an excellent linear correlation between heart rate and monophasic action potential duration. The ability of the method to detect drug-induced changes was confirmed using clofilium (10(-9) to 10(-5) M), which significantly prolonged monophasic action potential duration 50, 75, and 90 in a concentration-dependent manner, and tocainide (3 x 10(-4) M), which significantly decreased monophasic action potential duration 50, 75, and 90 and increased rise time.

摘要

已开发出一种体外技术用于记录单相动作电位,以测量已知浓度的药物和离子所引起的复极化持续时间和上升时间的变化。豚鼠心脏在恒压(60 cm H₂O)和恒温(37℃)下用克雷布斯 - 亨塞尔特缓冲液进行水平灌注。使用施加400 mmHg抽吸压力的双极银/氯化银电极从右心室基部记录心外膜单相动作电位。单相动作电位信号具有平滑的去极化和复极化阶段,幅度为25 - 65 mV;通过计算机分析确定的在复极化水平50%、75%和90%时的单相动作电位持续时间(MAPD 50、75和90)以及上升时间的重复测量值在至少150分钟的灌注过程中是可重复的。心率与单相动作电位持续时间之间存在极好的线性相关性。使用氯非铵(10⁻⁹至10⁻⁵ M)证实了该方法检测药物诱导变化的能力,氯非铵以浓度依赖性方式显著延长了单相动作电位持续时间50%、75%和90%,以及使用妥卡尼(3×10⁻⁴ M),妥卡尼显著缩短了单相动作电位持续时间50%、75%和90%并增加了上升时间。

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