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钾对豚鼠心脏中地高辛和洋地黄毒苷作用的差异效应。

Differential effect of potassium on the action of digoxin and digoxigenin in guinea-pig heart.

作者信息

Akera T, Wiest S A, Brody T M

出版信息

Eur J Pharmacol. 1979 Aug 15;57(4):343-51. doi: 10.1016/0014-2999(79)90497-7.

Abstract

The effect of potassium on the binding of digoxin or digoxigenin to isolated Na+, K+-ATPase was compared with that of potassium on the positive inotropic action of the agents in guinea-pig hearts. The binding of digoxigenin to the enzyme in vitro was reduced to a greater extent by potassium than was the binding of digotoxin. The digoxigenin-induced increase in the force of contraction of left atrial preparations estimated at steady state was reduced at higher potassium concentrations. Potassium had a lesser effect when digoxin was used as the inotropic agent. In contrast, potassium concentrations. Potassium had a lesser effect when digoxin was used as the ininotropic agent. In contrast, potassium reduced the rate of development and also the rate of loss of the positive inotropic action of digoxin observed with left atrial and Langendorff preparations, respectively, to a greater extent than those of digoxigenin. The loss of the positive inotropic effect was more rapid with digoxigenin than with digoxin at each KCl concentration. These data support the contention that the extent of the interaction of digitalis with Na+,K+-ATPase determines the degree of the positive inotropic effect.

摘要

将钾对地高辛或洋地黄毒苷与分离出的钠钾ATP酶结合的影响,与钾对豚鼠心脏中这些药物正性肌力作用的影响进行了比较。与地高辛的结合相比,钾在体外对洋地黄毒苷与该酶结合的降低程度更大。在较高钾浓度下,稳态时洋地黄毒苷诱导的左心房标本收缩力增加有所降低。当地高辛用作正性肌力药物时,钾的影响较小。相比之下,钾分别比洋地黄毒苷更大程度地降低了用左心房和Langendorff标本观察到的地高辛正性肌力作用的发展速率以及丧失速率。在每个氯化钾浓度下,洋地黄毒苷的正性肌力作用丧失比地高辛更快。这些数据支持了这样的论点,即洋地黄与钠钾ATP酶相互作用的程度决定了正性肌力作用的程度。

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