Stickney J L
Arch Int Pharmacodyn Ther. 1976 Dec;224(2):215-29.
Effects of three cardiac glycosides on the accumulation of 3H-1-noradrenaline (3H-1-NA) by slices of heart and spleen were studied. Ouabain, digitoxin and digoxin, all produced a concentration dependent inhibition of 3H-1-NA uptake in both types of tissue slices. The maximum amount of 3H-1-NA accumulated as well as the rate of uptake was decreased. Digitoxin and ouabain were equipotent; however, digoxin was significantly less potent. Tissues from different mamalian specis did not exhibit the same degree of sensitivity to the inhibitory effect of cardiac glycosides on 3H-1-NA accumulation. Dogs were most sensitive and guinea-pigs an order of magnitude less sensitive. Rats were least sensitive by roughly two orders of magnitude when compared with guinea-pigs. The relationship of the effect of digitalis on 3H-1-NA accumulation to digitalis-induced cardiac arrhythmias is discussed. Finally, the pattern of species sensitivity found here is compared with that observed in relation to inhibition of Na+-K+-ATPase by cardiac glycosides.
研究了三种强心苷对心脏和脾脏切片摄取³H-1-去甲肾上腺素(³H-1-NA)的影响。哇巴因、洋地黄毒苷和地高辛均对两种组织切片摄取³H-1-NA产生浓度依赖性抑制。³H-1-NA的最大蓄积量以及摄取速率均降低。洋地黄毒苷和哇巴因效力相当;然而,地高辛的效力明显较弱。来自不同哺乳动物物种的组织对强心苷抑制³H-1-NA蓄积的作用表现出不同程度的敏感性。狗最为敏感,豚鼠的敏感性低一个数量级。与豚鼠相比,大鼠的敏感性最低,约低两个数量级。讨论了洋地黄对³H-1-NA蓄积的作用与洋地黄诱导的心律失常之间的关系。最后,将此处发现的物种敏感性模式与强心苷抑制钠钾ATP酶时观察到的模式进行了比较。