Ogletree M L, Lefer A M
J Pharmacol Exp Ther. 1976 Jun;197(3):582-93.
Indomethacin, meclofenamic acid and acetylsalicylic acid are prostaglandin synthetase-inhibiting, nonsteroidal anti-inflammatory drugs. Their effects on hemodynamic and enzymatic responses to coronary artery occlusion were evaluated in the cat. The direct effects of these drugs on isolated tissue preparations (i.e., cat papillary muscle, aortic strip and liver lysosomes) were also studied. None of the drugs tested exhibited any significant hemodynamic or biochemical effects which would indicate protection against damage due to myocardial ischemia during the 5-hour experimental period. Furthermore, only indomethacin produced significant effects on the isolated tissues studied. Indomethacin increased the tension of aortic strips confirming a pressor effect seen in the intact animal and exerted a modest stabilization of isolated liver lysosomes. All three anti-inflammatory drugs inhibited prostaglandin F2alpha, release in heart homogenates by 82 to 87%. It is concluded that nonsteroidal anti-inflammatory drugs do not significantly influence the early course of myocardial ischemia in the cat, in contrast to the previously reported preservation of myocardial integrity afforded by dexamethasone and methylprednisolone.
吲哚美辛、甲氯芬那酸和乙酰水杨酸是抑制前列腺素合成酶的非甾体抗炎药。在猫身上评估了它们对冠状动脉闭塞时血流动力学和酶反应的影响。还研究了这些药物对离体组织制剂(即猫乳头肌、主动脉条和肝溶酶体)的直接作用。在5小时的实验期间,所测试的药物均未表现出任何显著的血流动力学或生化效应,表明对心肌缺血损伤无保护作用。此外,只有吲哚美辛对所研究的离体组织产生了显著影响。吲哚美辛增加了主动脉条的张力,证实了在完整动物中观察到的升压作用,并对离体肝溶酶体有适度的稳定作用。所有三种抗炎药均使心脏匀浆中前列腺素F2α的释放抑制82%至87%。结论是,与先前报道的地塞米松和甲泼尼龙对心肌完整性的保护作用相反,非甾体抗炎药对猫心肌缺血的早期进程没有显著影响。