Ravingerová T, Styk J, Trégerová V, Pancza D, Slezák J, Tribulová N, Ziegelhöffer A, Pissarek M, Szekeres L
Institute for Heart Research, Slovak Academy of Sciences, Bratislava, CSFR.
Basic Res Cardiol. 1991 May-Jun;86(3):245-53. doi: 10.1007/BF02190604.
The effect of 7-oxo PGI2 on function and metabolism of postischemic reperfused (30-min ischemia and 30-min reperfusion) rat hearts was studied with special regard to calcium overload as one of the main factors of the postischemic reperfusion damage to the heart. The drug (50 micrograms/kg i.p.) was applied 48 h prior to starting the experiments on isolated rat hearts (Langendorff preparation at 37 degrees C and constant perfusion pressure of 65 mm Hg). A late protective effect of 7-oxo PGI2 was manifested by an improved recovery of heart function during reperfusion and calcium overload, better preservation of myocardial ATP contents during ischemia and also after calcium overload, as well as by a normalization of the lactate content, otherwise extremely increased during ischemia. Electron microscopic data also supported the above results. The beneficial effect of pretreatment with PGI2 may be explained not only by its vasodilating action, but more by its membrane stabilizing effect with a consequently decreased sodium accumulation, potassium loss, as well as intracellular calcium overload.
研究了7-氧代前列环素(7-oxo PGI2)对缺血再灌注(30分钟缺血和30分钟再灌注)大鼠心脏功能和代谢的影响,特别关注钙超载这一缺血再灌注损伤心脏的主要因素之一。在对离体大鼠心脏(37℃下的Langendorff制备,恒定灌注压力为65mmHg)进行实验前48小时,腹腔注射该药物(50微克/千克)。7-氧代前列环素的晚期保护作用表现为再灌注期间心脏功能恢复改善和钙超载减轻,缺血期间以及钙超载后心肌ATP含量得到更好的保存,乳酸含量也恢复正常,否则在缺血期间乳酸含量会极度增加。电子显微镜数据也支持上述结果。PGI2预处理的有益作用不仅可以用其血管舒张作用来解释,更可以用其膜稳定作用来解释,从而减少钠积累、钾流失以及细胞内钙超载。