Hagerty M J, Wainwright C L, Kane K A
Department of Physiology and Pharmacology, University of Strathclyde, Glasgow, Scotland, UK.
J Pharm Pharmacol. 1996 Apr;48(4):417-21. doi: 10.1111/j.2042-7158.1996.tb05944.x.
AM 92016 (1-(4-methanesulphonamidophenoxy)- 3-(N-methyl-3-4-dichlorophenethylamino)-2-propanol benzoic acid salt), an oxypropanolamine analogue of sotalol, has been shown to possess Class III anti-arrhythmic properties in-vitro at concentrations showing 1000 times more potency than sotalol. The aim of this study was to characterize the effects of AM 92016 in-vivo. When administered to anaesthetized guinea-pigs, AM 92016 (10 micrograms kg-1 -5 mg kg-1) significantly increased heart rate, systolic arterial blood pressure, left ventricular systolic pressure and the contractile index dp dtmax. AM 92016 also significantly decreased the QT interval of the electrocardiogram from 135 +/- 10 to 105 +/- 4 ms (5 mg kg-1). The time to onset of the first arrhythmia and ventricular fibrillation, induced by intravenous infusion of ouabain, was shortened in the presence of AM 92016. Ouabain-induced ventricular fibrillation occurred at 18 +/- 5 and 12 +/- 3 min (P < 0.05) in control and AM 92016-(1 mg kg-1) treated guinea-pigs, respectively. An infusion of AM 92016 (2.5 micrograms kg-1 min-1) to anaesthetized pigs significantly increased the total number of arrhythmias occurring following coronary artery occlusion from 266 +/- 26 in control pigs to 535 +/- 148 (P < 0.05) in those receiving AM 92016. The time to onset of ventricular fibrillation was also significantly reduced in anaesthetized pigs from 24 +/- 1 to 18 +/- 3 min in the presence of AM 92016. The drug did not change haemodynamics in the anaesthetized pig. We conclude that AM 92016 exhibited proarrhythmic rather than antiarrhythmic activity when administered in-vivo to either guinea-pigs or pigs.
AM 92016(1-(4-甲磺酰胺苯氧基)-3-(N-甲基-3,4-二氯苯乙氨基)-2-丙醇苯甲酸盐)是索他洛尔的氧丙醇胺类似物,已证明其在体外具有Ⅲ类抗心律失常特性,其浓度下的效力比索他洛尔高1000倍。本研究的目的是表征AM 92016在体内的作用。给麻醉的豚鼠给药时,AM 92016(10微克/千克 - 5毫克/千克)显著增加心率、收缩期动脉血压、左心室收缩压和收缩指数dp/dtmax。AM 92016还显著缩短心电图的QT间期,从135±10毫秒降至105±4毫秒(5毫克/千克)。在存在AM 92016的情况下,静脉输注哇巴因诱发的首次心律失常和心室颤动的发作时间缩短。在对照豚鼠和接受AM 92016(1毫克/千克)治疗的豚鼠中,哇巴因诱发的心室颤动分别在第18±5分钟和第12±3分钟出现(P < 0.05)。给麻醉的猪输注AM 92016(2.5微克/千克·分钟)显著增加冠状动脉闭塞后出现的心律失常总数,从对照猪的266±26次增加到接受AM 92016的猪的535±148次(P < 0.05)。在存在AM 92016的情况下,麻醉猪的心室颤动发作时间也从24±1分钟显著缩短至18±3分钟。该药物未改变麻醉猪的血流动力学。我们得出结论,当在体内给豚鼠或猪给药时,AM 92016表现出促心律失常而非抗心律失常活性。