Förster W
Arch Int Pharmacodyn Ther. 1975 Sep;217(1):152-61.
Experimental studies on BaCl2 induced arrhythmias in unanaesthetized rabbits showed an antiarrhythmic effect of prostaglandins A1, A2, E1, E2 and F2a by infusions of 0,1 to 6,0 mug/kg/min over 3 min. There was a maximum antiarrhythmic effect between 50% and 80%. Ajmaline was similarly effective when given in doses 100-1000 times higher. PGA1 and PGE2 were most effective in this model; the ED50-values of the other PGs were 2-3 times higher. The mode of action of PGs is unknown; the following factors are discussed: the influence on the ionic movements, the negative feedback mechanism on the release of adrenergic transmitter and central nervous effects.
对未麻醉家兔进行的氯化钡诱发心律失常的实验研究表明,通过以0.1至6.0微克/千克/分钟的速度输注3分钟,前列腺素A1、A2、E1、E2和F2α具有抗心律失常作用。在50%至80%之间存在最大抗心律失常作用。当给予剂量高100 - 1000倍的阿义马林时,其效果相似。PGA1和PGE2在该模型中最有效;其他前列腺素的ED50值高2 - 3倍。前列腺素的作用方式尚不清楚;讨论了以下因素:对离子运动的影响、对肾上腺素能递质释放的负反馈机制以及中枢神经效应。