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[人参皂苷Rg1和杠柳毒苷对Na +,K(+)-ATP酶的抑制作用]

[Inhibitory action of peruvoside and neriifolin on Na+, K(+)-ATPase].

作者信息

Ye Y X, Yang X R

机构信息

Institute of Basic Medical Sciences, Chinese Academy of Medical Sciences, Beijing.

出版信息

Zhongguo Yao Li Xue Bao. 1990 Nov;11(6):491-4.

PMID:1966653
Abstract

Effects of peruvoside and neriifolin, main components of neriperside, a tevetoside extracted from Thevitia neriifolia Juss, on Na+, K(+)-ATPase activities and on [3H] ouabain binding to the Na+, K(+)-ATPase isolated from hearts of guinea pigs, dogs and cats and kidneys of guinea pigs and cats were compared with digoxin and ouabain. It was found that peruvoside and neriifolin inhibited Na+, K(+)-ATPase activities and they showed a strong competitive inhibition on [3H] ouabain binding to the enzymes isolated from various tissues. A marked species difference existed as great as that of digitalis. The mechanism of action of these 2 drugs may be similar to that of digitalis. Their inhibitory effects on the enzyme activity were stronger than their positive inotropic effects, while both actions of digitalis were parallel quantitatively. There may be some differences in the modulation of the intracellular Ca2+ between neripersides and digitalis.

摘要

从黄花夹竹桃(Thevitia neriifolia Juss)中提取的强心苷类化合物黄夹苷中的主要成分黄夹次苷和去乙酰黄夹次苷,对豚鼠、犬、猫心脏以及豚鼠和猫肾脏中分离出的Na⁺,K⁺-ATP酶活性及[³H]哇巴因与该酶的结合作用的影响,与地高辛和哇巴因进行了比较。结果发现,黄夹次苷和去乙酰黄夹次苷可抑制Na⁺,K⁺-ATP酶活性,并对从各种组织中分离出的酶上的[³H]哇巴因结合表现出强烈的竞争性抑制作用。存在与洋地黄一样显著的种属差异。这两种药物的作用机制可能与洋地黄相似。它们对酶活性的抑制作用强于其正性肌力作用,而洋地黄的这两种作用在数量上是平行的。在细胞内Ca²⁺调节方面,黄夹苷类化合物和洋地黄之间可能存在一些差异。

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