Ghysel-Burton J, Godfraind T
Br J Pharmacol. 1979 Jun;66(2):175-84. doi: 10.1111/j.1476-5381.1979.tb13662.x.
1 The actions of ouabain, ouabagenin and dihydroouabain on the contractility and on the ionic content have been investigated in left guinea-pig atria stimulated at 3.3 Hz. The specific binding of ouabain and its displacement by the other cardenolides have been determined. 2 The action of either ouabain or ouabagenin on Na and K content was qualitatively different according to the concentration employed. Low doses evoked a reduction of Nai whereas high doses produced an increase. Dihydroouabain evoked only a Nai gain. 3 The increase of KCl concentration from 2.7 to 12 mM decreased Nai in untreated atria and displaced ouabain dose-effect curves to the right. 4 ED50 values for the positive inotropic effect were lower than ED50 values for the inhibition of the pump and were not similarly affected by an increase in KCl concentration. 5 The specific binding of ouabain occurred at high and low affinity sites, related to Na pump stimulation and inhibition respectively. 6 The increase in KCl reduced the affinity of the two groups of sites for ouabain and increased the capacity of the high-affinity sites whereas the capacity of the other sites remained unchanged. 7 The results confirm the existence of two specific binding sites for ouabain in guinea-pig heart and suggest that the inhibition of the Na pump is not the only mechanism responsible for the positive inotropic effect of cardiac glycosides.
研究了哇巴因、哇巴苷元和二氢哇巴因对3.3Hz刺激的豚鼠左心房收缩性和离子含量的影响。测定了哇巴因的特异性结合及其被其他强心苷类的置换情况。
哇巴因或哇巴苷元对钠和钾含量的作用根据所用浓度在性质上有所不同。低剂量引起细胞内钠(Nai)减少,而高剂量则使其增加。二氢哇巴因仅引起细胞内钠增加。
氯化钾浓度从2.7mM增加到12mM可使未处理心房中的细胞内钠减少,并使哇巴因剂量效应曲线右移。
正性肌力作用的半数有效剂量(ED50)值低于抑制泵的ED50值,且不受氯化钾浓度增加的类似影响。
哇巴因的特异性结合发生在高亲和力和低亲和力位点,分别与钠泵的刺激和抑制有关。
氯化钾浓度增加降低了两组位点对哇巴因的亲和力,增加了高亲和力位点的容量,而其他位点的容量保持不变。
结果证实豚鼠心脏中存在两个哇巴因特异性结合位点,并表明抑制钠泵不是强心苷正性肌力作用的唯一机制。