Michaels D C, Kabela E
Recent Adv Stud Cardiac Struct Metab. 1975;5:367-74.
To test hypotheses relating positive inotropic effects of cardiac glycosides (CG) to inhibitory effects on Na,K-ATPase, cardiac actions of other inhibitors were examined. Ethacrynic acid was studied using microelectrode recordings of dog Purkinje fibers (DP) and cat papillary muscle (CP), and isometric recordings of CP at Lmax stimulated at 1/sec (36.5 degrees C). Results with all doses (20-200 gamma/ml) were similar, differing only in latency. Actions of ethacrynic acid on electrical activity of DP and CP were, chronologically: increase in duration of the action potential (AP), and decrease in dV/dt, overshoot, and resting potential. In CP an initial increase (2-5 min) in contractility (10-15 percent) was followed by decreased in active tension and dP/dt with parallel increases in resting tension and duration of contraction. ATP levels were unchanged, eliminating the possibility of ethacrynic acid acting as a metabolic poison. Simultaneous recording of contractions and AP in CP showed that the positive inotropic effect was always associated with a lengthening of the AP. In a series of CP, ouabain (2 gamma/ml) always increased contractility when ethacrynic acid had already reduced it by 75 percent. These results suggest that Na,K-ATPase inhibition is not responsible for the inotropic effects of CG.
为了检验关于强心苷(CG)的正性肌力作用与对钠钾ATP酶的抑制作用之间关系的假说,研究了其他抑制剂的心脏作用。使用狗浦肯野纤维(DP)和猫乳头肌(CP)的微电极记录,以及在36.5℃下以1次/秒刺激的CP在最大张力(Lmax)时的等长记录,对依他尼酸进行了研究。所有剂量(20 - 200微克/毫升)的结果相似,仅在潜伏期有所不同。依他尼酸对DP和CP电活动的作用按时间顺序依次为:动作电位(AP)持续时间增加,dV/dt、超射和静息电位降低。在CP中,收缩力最初增加(2 - 5分钟)(10 - 15%),随后主动张力和dP/dt降低,同时静息张力和收缩持续时间平行增加。ATP水平未改变,排除了依他尼酸作为代谢毒物起作用的可能性。在CP中同时记录收缩和AP表明,正性肌力作用总是与AP延长相关。在一系列CP实验中,当依他尼酸已经使收缩力降低75%时,哇巴因(2微克/毫升)总是能增加收缩力。这些结果表明,钠钾ATP酶抑制并非强心苷正性肌力作用的原因。