Grover G J, Schumacher W A, Ogletree M L
Department of Pharmacology, Bristol-Myers Squibb Pharmaceutical Research Institute, Princeton, New Jersey 08543-4000.
J Cardiovasc Pharmacol. 1994 Sep;24(3):493-9. doi: 10.1097/00005344-199409000-00019.
We determined the effect of thromboxane A2 (TXA2) prostaglandin endoperoxide (TP) receptor antagonism, using BMS-180291 or aspirin, on the severity of pacing-induced ischemia in anesthetized dogs. Thromboxane receptor antagonists may not only have antithrombotic activity, but may also have direct cardioprotective effects, unlike aspirin. Left anterior descending coronary artery (LAD) stenosis was adjusted so that a significant (10-12 mV) ST segment elevation was observed only when superimposed on atrial pacing. Each heart was subjected to 5-min episodes of pacing-induced ischemia 10, 40, and 70 min after initiation of BMS-180291 (1 mg/kg + 1 mg/kg/h) or vehicle. In the vehicle group, ST segment elevation was reproducible at all pacing-induced ischemia episodes, whereas BMS-180291 significantly reduced it by 30% at the later ischemia episodes. This reduction in ST segment increase was not accompanied by alterations in regional myocardial blood flow (RMBF) nor in hemodynamic status. Aspirin in the same model [10 mg/kg intravenously (i.v.) given 10 min before pacing-induced ischemia] did not significantly reduce ST segment elevation, indicating a lack of protective effect in this model. Thromboxane receptor blockade appears to protect myocardium subjected to pacing-induced ischemia, an effect not produced by aspirin.
我们使用BMS-180291或阿司匹林,确定了血栓素A2(TXA2)前列腺素内过氧化物(TP)受体拮抗作用对麻醉犬起搏诱导的缺血严重程度的影响。与阿司匹林不同,血栓素受体拮抗剂不仅可能具有抗血栓活性,还可能具有直接的心脏保护作用。调整左前降支冠状动脉(LAD)狭窄程度,使得仅在心房起搏时才观察到显著的(10 - 12 mV)ST段抬高。在开始给予BMS-180291(1 mg/kg + 1 mg/kg/h)或赋形剂后10、40和70分钟,对每颗心脏进行5分钟的起搏诱导缺血发作。在赋形剂组中,所有起搏诱导的缺血发作时ST段抬高均可重现,而BMS-180291在后期缺血发作时使其显著降低了30%。ST段升高的这种降低并未伴有局部心肌血流量(RMBF)或血流动力学状态的改变。在同一模型中,阿司匹林[在起搏诱导缺血前10分钟静脉注射(i.v.)10 mg/kg]并未显著降低ST段抬高,表明在该模型中缺乏保护作用。血栓素受体阻断似乎可保护遭受起搏诱导缺血的心肌,这一作用阿司匹林无法产生。