Wright R A, Decroly P, Kharkevitch T, Oliver M F
Cardiovascular Research Unit, University of Edinburgh, Scotland.
Cardiovasc Drugs Ther. 1993 Dec;7(6):929-34. doi: 10.1007/BF00877729.
In a double-blind, placebo-controlled, randomized trial of treadmill exercise tolerance in six patients with chronic stable angina, intravenous mivazerol 1 microgram, 2 micrograms, and 3 micrograms/kg increased the time to onset of angina by 39%, 48%, and 76%; the time to 1-mm ST depression by 36%, 76%, and 104%; and total exercise duration by 15%, 23%, and 30%, respectively. In a subsequent double-blind, placebo-controlled, randomized trial involving a further 12 patients, a single oral dose of mivazerol of 800 micrograms, 1200 micrograms, and 1600 micrograms increased the time to onset of angina by 4%, 11%, and 30%; the time to 1-mm ST depression by 33%, 43%, and 53%; and the total exercise duration by 10%, 18%, and 23%, respectively. Mivazerol is an imidazole derivative with agonist properties at the alpha 2-adrenoceptor and appears to be an effective antianginal. Mivazerol may improve exercise performance by attenuating the effects of exercise-induced sympathetic nervous system activity on the ischemic myocardium.
在一项针对6例慢性稳定型心绞痛患者的跑步机运动耐量双盲、安慰剂对照、随机试验中,静脉注射米伐洛尔1微克/千克、2微克/千克和3微克/千克,使心绞痛发作时间分别延长39%、48%和76%;使出现1毫米ST段压低的时间分别延长36%、76%和104%;使总运动持续时间分别延长15%、23%和30%。在随后一项涉及另外12例患者的双盲、安慰剂对照、随机试验中,单次口服800微克、1200微克和1600微克米伐洛尔,使心绞痛发作时间分别延长4%、11%和30%;使出现1毫米ST段压低的时间分别延长33%、43%和53%;使总运动持续时间分别延长10%、18%和23%。米伐洛尔是一种咪唑衍生物,对α2肾上腺素能受体具有激动剂特性,似乎是一种有效的抗心绞痛药物。米伐洛尔可能通过减弱运动诱导的交感神经系统活动对缺血心肌的影响来改善运动表现。