Ravingerová T, Tribulová N, Ziegelhöffer A
Institute for Heart Research, Slovak Academy of Sciences, Bratislava.
Life Sci. 1993;53(16):1309-16. doi: 10.1016/0024-3205(93)90576-o.
Protective effect of a stable derivative of prostacyclin (7-oxo PGI2) was studied on the model of calcium overload (Ca paradox) 48 h after i.m. administration of the drug in a dosage of 50 micrograms/kg. In isolated rat heart perfused at 37 degrees C and a constant perfusion pressure of 65 mm Hg (Langendorff preparation) Ca paradox was induced by a 3 min perfusion with a calcium-free Krebs-Henseleit (KH) solution and followed by a 10 min perfusion with KH containing normal concentration of calcium. Late protective effect of 7-oxo PGI2 was manifested by: i. improved recovery of heart function (developed pressure and coronary flow) after Ca paradox, ii. better preservation of macroergic phosphates content, iii. better preserved cardiac ultrastructure (sarcolemma) already during Ca depletion phase. One of the proposed mechanisms of the protection afforded by the pretreatment with 7-oxo PGI2 may be that the cell membrane and possibly the intercalated discs become less affected by calcium depletion, resulting in less contracture-mediated membrane damage upon calcium repletion.
在以50微克/千克的剂量肌肉注射药物48小时后,研究了前列环素的一种稳定衍生物(7-氧代前列环素2)对钙超载(钙反常)模型的保护作用。在37℃和65毫米汞柱的恒定灌注压力下灌注分离的大鼠心脏(Langendorff标本),通过用无钙的克雷布斯-亨泽莱特(KH)溶液灌注3分钟诱导钙反常,随后用含正常浓度钙的KH溶液灌注10分钟。7-氧代前列环素2的后期保护作用表现为:i. 钙反常后心脏功能(舒张压力和冠状动脉血流量)的恢复改善;ii. 高能磷酸盐含量的更好保存;iii. 在钙耗竭阶段已经更好地保存了心脏超微结构(肌膜)。用7-氧代前列环素2预处理提供保护的一种可能机制可能是细胞膜以及可能的闰盘受钙耗竭的影响较小,从而在钙再灌注时由挛缩介导的膜损伤较小。