Smith E F, Kloster G, Stöcklin G, Schrör K
Biomed Biochim Acta. 1984;43(8-9):S155-8.
The hypothesis that prostacyclins exert a membrane stabilizing action on the ischemic myocardium was examined in isolated rabbit hearts by measuring the elimination half-time of labelled catabolites after injection of 17-(131I)-heptadecanoic acid. During normoxia, a rapid washout of labelled lipids was observed along with a slower exponential elimination of I- from beta-oxidation. After 90 min of ischemia, lipid washout was increased over 6-fold. Infusion of iloprost (1.1 nmol/min) significantly reduced the lipid washout half-time. Iloprost preserved functional myocardial integrity as evidenced by a greater recovery of left ventricular pressure and attenuation of the increase in coronary resistance after reperfusion. These results indicate that the poor recovery of the heart after ischemia is associated with significant changes in membrane integrity and permeability. These data support the hypothesis that the biochemical and functional myocardial preservation by prostacyclin(s) is by a membrane stabilizing mechanism.
通过测量注射17-(¹³¹I)-十七烷酸后标记代谢物的消除半衰期,在离体兔心脏中检验了前列环素对缺血心肌发挥膜稳定作用的假说。在常氧期间,观察到标记脂质的快速洗脱以及来自β-氧化的碘的较慢指数消除。缺血90分钟后,脂质洗脱增加了6倍以上。输注依洛前列素(1.1 nmol/分钟)显著缩短了脂质洗脱半衰期。依洛前列素维持了心肌功能完整性,这可通过左心室压力的更大恢复以及再灌注后冠状动脉阻力增加的减轻来证明。这些结果表明,缺血后心脏恢复不良与膜完整性和通透性的显著变化有关。这些数据支持了以下假说,即前列环素对心肌的生化和功能保护是通过膜稳定机制实现的。