洋地黄苷在亚细胞水平的作用机制。 - Suppr

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Mechanism of action of digitalis glycosides at the subcellular level.

作者信息

Lindenmayer G E

出版信息

Pharmacol Ther B. 1976;2(4):843-61. doi: 10.1016/0306-039x(76)90081-7.

DOI:10.1016/0306-039x(76)90081-7

PMID:138142

Abstract

摘要

相似文献

Mechanism of action of digitalis glycosides at the subcellular level.洋地黄苷在亚细胞水平的作用机制。

Pharmacol Ther B. 1976;2(4):843-61. doi: 10.1016/0306-039x(76)90081-7.

Inotropic action of digitalis and ion transport.洋地黄的变力作用与离子转运

Life Sci. 1976 Jan 15;18(2):135-44. doi: 10.1016/0024-3205(76)90017-5.

[Cardiac glycoside-induced inhibition of membrane ATPase as a cause of digitalis intoxication].[强心苷诱导的膜ATP酶抑制作为洋地黄中毒的一个原因]

Med Klin. 1975 Jul 4;70(27):1166-73.

The role of Na+,K+-ATPase in the inotropic action of digitalis.钠钾ATP酶在洋地黄正性肌力作用中的角色。

Pharmacol Rev. 1977 Sep;29(3):187-220.

A kinetic characterization of calcium on (Na+ + K+)-ATPase and its potential role as a link between extracellular and intracellular events: hypothesis for digitalis-induced inotropism.钙对（钠+钾）-ATP酶的动力学特性及其作为细胞外与细胞内事件之间联系的潜在作用：关于洋地黄诱导的变力作用的假说

J Mol Cell Cardiol. 1975 Aug;7(8):591-612. doi: 10.1016/0022-2828(75)90117-0.

Membrane adenosinetriphosphatase: a digitalis receptor?膜腺苷三磷酸酶：一种洋地黄受体？

Science. 1977 Nov 11;198(4317):569-74. doi: 10.1126/science.144320.

Is the cell membrane Na+, K+ -ATPase enzyme system the pharmacological receptor for digitalis?细胞膜钠钾ATP酶系统是洋地黄的药理受体吗？

Circ Res. 1976 Jul;39(1):1-7. doi: 10.1161/01.res.39.1.1.

[Basis of the active mechanism of cardioactive glycoside].[强心苷活性机制的基础]

Verh Dtsch Ges Inn Med. 1977;83:6-18.

Role of Na+-K+-activated adenosine triphosphatase in the transmembrane transport of K+ and Na+: relationships to the inotropic and electrophysiologic effects of digitalis.钠钾激活的三磷酸腺苷酶在钾离子和钠离子跨膜转运中的作用：与洋地黄的变力性和电生理效应的关系。

Recent Adv Stud Cardiac Struct Metab. 1974;4:107-17.

[Chemistry, biochemistry and clinical pharmacology of digitalis glycosides. An overview].[洋地黄苷类的化学、生物化学与临床药理学。综述]

Arzneimittelforschung. 1973 Oct;23(10):1439-46.

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Purification from human plasma of endogenous sodium transport inhibitor(s).从人血浆中纯化内源性钠转运抑制剂。

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Lipophilicity and pharmacodynamics of cardiotonic steroids in guinea-pig isolated heart muscle preparations.强心甾类化合物在豚鼠离体心肌制剂中的亲脂性和药效学

Br J Pharmacol. 1988 Feb;93(2):281-8. doi: 10.1111/j.1476-5381.1988.tb11432.x.

Digitalis cardiotoxicity: cellular calcium overload a possible mechanism.洋地黄心脏毒性：细胞钙超载——一种可能的机制

Basic Res Cardiol. 1989 Nov-Dec;84(6):553-63. doi: 10.1007/BF01906941.

Correlation between inhibition of (Na+, K+)-membrane-ATPase and positive inotropic activity of cardenolides in isolated papillary muscles of guinea pig.豚鼠离体乳头肌中强心苷对（钠，钾）-膜ATP酶的抑制作用与正性肌力活性之间的相关性。

Naunyn Schmiedebergs Arch Pharmacol. 1978 Aug;304(1):37-44. doi: 10.1007/BF00501375.

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