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哇巴因对3H-1-去甲肾上腺素摄取的抑制作用具有种属依赖性。

Inhibition of 3H-1-norepinephrine uptake by ouabain is species dependent.

作者信息

Stickney J L

出版信息

Res Commun Chem Pathol Pharmacol. 1976 Jun;14(2):227-36.

PMID:940956
Abstract

Tissue slice to medium ratios of 3H-1-norepinephrine (3H-1-NE) were used to study the effect of ouabain on uptake of norepinephrine. The effects of ouabain were studied in slices of heart and spleen from three different species: rat, guinea pig, and dog. The drug produced a species as well as a concentration dependent inhibition of norepinephrine uptake in both types of tissue. In order of decreasing sensitivity, the following relationship between species was observed: dogs greater than guinea pigs greater than rats. Since 3H-1-norepinephrine uptake under the present experimental conditions represents uptake into sympathetic nerve terminals, it was concluded that Na+-K+-ATPases of sympathetic nerve terminals have species dependent differences in ouabain sensitivity similar to those of myocardium.

摘要

使用3H-1-去甲肾上腺素(3H-1-NE)的组织切片与培养基比例来研究哇巴因对去甲肾上腺素摄取的影响。在来自三种不同物种(大鼠、豚鼠和狗)的心脏和脾脏切片中研究了哇巴因的作用。该药物对两种组织中的去甲肾上腺素摄取均产生了物种及浓度依赖性抑制。按敏感性降低的顺序,观察到物种之间存在以下关系:狗>豚鼠>大鼠。由于在当前实验条件下3H-1-去甲肾上腺素的摄取代表其进入交感神经末梢,因此得出结论,交感神经末梢的Na+-K+-ATP酶在哇巴因敏感性方面具有与心肌类似的物种依赖性差异。

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