Grover G J, Parham C S, Schumacher W A
Department of Pharmacology, Squibb Institute for Medical Research, Princeton, New Jersey.
Basic Res Cardiol. 1991 Mar-Apr;86(2):99-106. doi: 10.1007/BF02190542.
A previous study indicated that 5 mg/kg aspirin can reverse the cardioprotective effects of thromboxane A2 synthetase inhibitors. We determined in the present study if this dose of aspirin can also reverse the protective effects of the thromboxane A2/PGH2 receptor antagonist SQ 30,741 in the same model of coronary occlusion and reperfusion. Anesthetized dogs were subjected to 90 min of coronary occlusion and 5 h of reperfusion and were treated with vehicle or SQ 30,741 (1 mg/kg + 1 mg/kg/h) 10 min after the onset of coronary occlusion. SQ 30,741 was given to dogs pretreated with aspirin (5 mg/kg, 24 h presurgery) or vehicle. SQ 30,741 significantly reduced infarct size compared to vehicle treatment (58% vs 35% of the left ventricular area at risk for vehicle and SQ 30,741 groups respectively) and aspirin did not reverse this. These anti-ischemic effects occurred despite a lack of change in collateral flow. Thus, important differences in mechanism of action between thromboxane synthesis inhibitors and receptor antagonists seem to exist and further work in this area is warranted.
先前的一项研究表明,5毫克/千克的阿司匹林可逆转血栓素A2合成酶抑制剂的心脏保护作用。在本研究中,我们确定了在相同的冠状动脉闭塞和再灌注模型中,该剂量的阿司匹林是否也能逆转血栓素A2/前列腺素H2受体拮抗剂SQ 30,741的保护作用。对麻醉的犬进行90分钟的冠状动脉闭塞和5小时的再灌注,并在冠状动脉闭塞开始后10分钟用赋形剂或SQ 30,741(1毫克/千克+1毫克/千克/小时)进行治疗。将SQ 30,741给予用阿司匹林(5毫克/千克,术前24小时)或赋形剂预处理的犬。与赋形剂治疗相比,SQ 30,741显著减小了梗死面积(赋形剂组和SQ 30,741组分别为左心室危险区域的58%和35%),而阿司匹林并未逆转这一效果。尽管侧支血流没有变化,但仍出现了这些抗缺血作用。因此,血栓素合成抑制剂和受体拮抗剂之间似乎存在重要的作用机制差异,该领域值得进一步开展研究。