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心肌选择性α1肾上腺素能受体拮抗剂UK-52046和阿替洛尔单独及联合应用对犬实验性心律失常的影响。

Effects of the myocardial-selective alpha 1-adrenoceptor antagonist UK-52046 and atenolol, alone and in combination, on experimental cardiac arrhythmias in dogs.

作者信息

Uprichard A G, Harron D W, Wilson R, Shanks R G

机构信息

Department of Therapeutics and Pharmacology, Queen's University of Belfast, Northern Ireland.

出版信息

Br J Pharmacol. 1988 Dec;95(4):1241-54. doi: 10.1111/j.1476-5381.1988.tb11761.x.

Abstract
  1. Adrenaline-induced arrhythmias in anaesthetized dogs respired with halothane were attenuated in 3 groups of 6 dogs by either UK-52046, 3.8 +/- 1.4 micrograms kg-1 (mean +/- s.e.mean), atenolol 14.6 +/- 2.1 micrograms kg-1, or a combination containing equal amounts of the two drugs of 0.36 +/- 0.1 microgram kg-1. The pressor response to adrenaline was reduced (P less than 0.01) by UK-52046 but not by atenolol or the combination of both drugs. 2. In a group of 6 dogs with multiventricular ectopic beats 24 h after coronary artery ligation (CAL), UK-52046, 32 micrograms kg-1, increased the number of sinus beats in each 5 min period from 137 +/- 47 to 662 +/- 99 (P less than 0.01); this was associated with a significant (P less than 0.01) fall in blood pressure. Atenolol in doses of up to 800 micrograms kg-1 had no effect. 3. UK-52046, 3.7 +/- 1.4 micrograms kg-1, prevented adrenaline-induced arrhythmias 3-4 days after CAL in 6/6 conscious dogs; atenolol in doses of up to 100 micrograms kg-1 produced an 84.4 +/- 7.4% reduction in the number of ventricular ectopic beats. A combination containing 3.7 +/- 1.1 micrograms kg-1 of each drug prevented the arrhythmia in 6/6 dogs. The pressor response to adrenaline was attenuated (P less than 0.05) by UK-52046, but resting blood pressure was unaffected by the different treatments. An increase (P less than 0.01) in heart rate was associated with both UK-52046 and the combination. 4. Neither UK-52046 (doses up to 64 micrograms kg-1) nor atenolol (up to 800 micrograms kg-1) had any effect upon ouabain-induced arrhythmias in 2 groups of 6 anaesthetized dogs. 5. In a study of the early (1a/1b) arrhythmias of acute myocardial ischaemia, the total number of ventricular ectopic beats occurring within 30 min of CAL was not reduced by 4 micrograms kg-1 UK-52046 but fell (P less than 0.01 compared with placebo) after 8 micrograms kg-1 [median values with ranges for placebo, 4 micrograms kg-1 and 8 micrograms kg-1 respectively 190 (4-674), 246 (9-1204) and 12 (1-154)]. Both doses of UK-52046 were associated with significant falls in blood pressure. 6. The arrhythmias produced by programmed electrical stimulation were studied in 2 groups of 6 conscious dogs, 7-30 days after CAL. With placebo, 4/6 dogs remained unchanged and 2 died: UK-52046 prevented arrhythmias in 2/6, 2 remained unchanged and 2 died (P = 0.29). Compared with placebo, blood pressure fell with doses greater than 4jg kg- '. 7. These results indicate antiarrhythmic effects of UK-52046 in a number of experimental models and suggest an enhanced role of alpha-receptors in the genesis of ischaemia-related arrhythmias. In several of the models used, UK-52046 produced haemodynamic changes in keeping with peripheral alpha-adrenoceptor antagonism.
摘要
  1. 用氟烷通气麻醉的犬,静脉注射肾上腺素诱发心律失常。6只犬为一组,共3组,分别给予UK - 52046(3.8±1.4微克/千克,均值±标准误均值)、阿替洛尔(14.6±2.1微克/千克)或两种药物等量组合(0.36±0.1微克/千克)后,心律失常均减轻。UK - 52046可降低对肾上腺素的升压反应(P<0.01),但阿替洛尔及两种药物的组合则无此作用。2. 一组6只犬在冠状动脉结扎(CAL)24小时后出现多源性室性早搏,给予UK - 52046(32微克/千克)后,每5分钟的窦性心搏数从137±47增加至662±99(P<0.01);同时血压显著下降(P<0.01)。给予高达800微克/千克剂量的阿替洛尔则无此作用。3. 6只清醒犬在CAL后3 - 4天,给予UK - 52046(3.7±1.4微克/千克)可预防肾上腺素诱发的心律失常;给予高达100微克/千克剂量的阿替洛尔可使室性早搏数减少84.4±7.4%。两种药物各含3.7±1.1微克/千克的组合可使6只犬均预防心律失常。UK - 52046可减弱对肾上腺素的升压反应(P<0.05),但不同治疗对静息血压无影响。UK - 52046及组合用药均可使心率增加(P<0.01)。4. 两组6只麻醉犬,给予高达64微克/千克剂量的UK - 52046或高达800微克/千克剂量的阿替洛尔,对哇巴因诱发的心律失常均无作用。5. 在急性心肌缺血早期(1a/1b)心律失常的研究中,CAL后30分钟内,给予4微克/千克的UK - 52046未减少室性早搏总数,但给予8微克/千克后室性早搏总数减少(与安慰剂相比P<0.01)[安慰剂、4微克/千克和8微克/千克的中位数及范围分别为190(4 - 674)、246(9 - 1204)和12(1 - 154)]。两种剂量的UK - 52046均使血压显著下降。6. 在两组6只清醒犬中研究了CAL后7 - 30天程序电刺激诱发的心律失常。给予安慰剂时,6只犬中有4只未改变,2只死亡;给予UK - 52046时,6只犬中有2只预防了心律失常,2只未改变,2只死亡(P = 0.29)。与安慰剂相比,剂量大于4微克/千克时血压下降。7. 这些结果表明UK - 52046在多个实验模型中具有抗心律失常作用,并提示α受体在缺血相关性心律失常的发生中作用增强。在所用的几个模型中,UK - 52046产生的血流动力学变化符合外周α - 肾上腺素能受体拮抗作用。

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