Allely M C, Alps B J
Department of Pharmacology, Syntex Research Centre, Riccarton, Edinburgh.
Br J Pharmacol. 1990 Jan;99(1):5-6. doi: 10.1111/j.1476-5381.1990.tb14641.x.
In control anaesthetized baboons subjected to 30 min occlusion of the left anterior descending coronary artery, followed by 5.5 h reperfusion, total plasma levels for creatine kinase (CK) and lactate dehydrogenase (LDH) were markedly elevated in a time-related manner. In a second group of baboons pretreated 10 min prior to ischaemia with ranolazine [(+/-)-N-(2,6-dimethyl-phenyl)-4[2-hydroxy-3-(2-methoxyphenoxy)propyl]-1 - piperazine acetamide dihydrochloride; RS-43285-193] at 500 micrograms kg-1 i.v., followed by continuous infusion of 50 micrograms kg-1 min-1, neither enzyme was significantly elevated at any time point. Similarly, serum levels of the cardiospecific isoenzyme CK2 were 8 fold greater in the controls than in the ranolazine-treated animals at 6 h. The results indicate that ranolazine pretreatment abolished cardiac enzyme release over a 5.5 h reperfusion period, indicating a potential protective effect.
在接受左冠状动脉前降支闭塞30分钟,随后再灌注5.5小时的对照麻醉狒狒中,肌酸激酶(CK)和乳酸脱氢酶(LDH)的血浆总水平呈时间依赖性显著升高。在第二组狒狒中,在缺血前10分钟静脉注射雷诺嗪[(±)-N-(2,6-二甲基苯基)-4-[2-羟基-3-(2-甲氧基苯氧基)丙基]-1-哌嗪乙酰胺二盐酸盐;RS-43285-193],剂量为500微克/千克,随后以50微克/千克·分钟的速度持续输注,在任何时间点两种酶均未显著升高。同样,在6小时时,对照组心脏特异性同工酶CK2的血清水平比接受雷诺嗪治疗的动物高8倍。结果表明,雷诺嗪预处理在5.5小时的再灌注期内消除了心脏酶的释放,表明其具有潜在的保护作用。