The role of potassium in the inhibition by cardiac glycosides of (Na+-K+)-ATPase prepared from human heart [(proceedings)].
作者信息
De Pover A, Godfraind T
出版信息
Br J Pharmacol. 1976 Nov;58(3):413P-414P.
Abstract
摘要
相似文献
1
The role of potassium in the inhibition by cardiac glycosides of (Na+-K+)-ATPase prepared from human heart [(proceedings)].钾在强心苷对人心脏制备的（钠-钾）-ATP酶抑制作用中的角色[会议论文集]
Br J Pharmacol. 1976 Nov;58(3):413P-414P.
2
Cardiac glycoside sensitivity of (Na + +K + )-activated ATPase in new-born rats.新生大鼠中（钠+钾）激活的ATP酶的强心苷敏感性
Res Commun Chem Pathol Pharmacol. 1972 Nov;4(3):699-706.
3
Sensitivity to cardiac glycosides of (Na + K) ATPase prepared from human heart, guinea-pig heart and guinea-pig brain.
Arch Int Pharmacodyn Ther. 1976 Jun;221(2):339-41.
4
Na+, K+-ATPase, cardiac glycosides, and heart function.钠钾ATP酶、强心苷与心脏功能
Ann N Y Acad Sci. 1974;242(0):740-1. doi: 10.1111/j.1749-6632.1974.tb19136.x.
5
Effect of some Pteridine compounds on the Na+ + K+)-ATPase and on the cardiac glycoside receptor of human heart).某些蝶啶化合物对人心脏的（钠 + 钾）-ATP酶及强心苷受体的作用。
Arzneimittelforschung. 1978;28(2):298-9.
6
The inhibition of the Na-K-ATPase of guinea-pig heart microsomes by cardiac glycosides.强心苷对豚鼠心脏微粒体钠钾ATP酶的抑制作用。
Arch Int Pharmacodyn Ther. 1973 Jan;201(1):197-200.
7
Na, K-activated ATPase activity during and after arrhythmic response to AY-22-241 in the canine heart.犬心脏对AY - 22 - 241心律失常反应期间及之后的钠钾激活ATP酶活性
Ann N Y Acad Sci. 1974;242(0):671-82. doi: 10.1111/j.1749-6632.1974.tb19125.x.
8
[New aspects on the mode of action of cardiac glycosides].[强心苷作用机制的新进展]
Fortschr Med. 1976 Nov 11;94(32):1037-45.
9
The subcellular basis for the mechanism of inotropic action of cardiac glycosides.强心苷正性肌力作用机制的亚细胞基础。
Pharmacol Rev. 1971 Sep;23(3):193-261.
10
Mechanism of cardiac glycoside inhibition of the (Na+-K+)-dependent ATPase from cardiac tissue.强心苷对心脏组织中依赖（Na⁺-K⁺）的ATP酶的抑制机制。
Biochim Biophys Acta. 1968 Mar 25;151(3):655-63. doi: 10.1016/0005-2744(68)90013-2.
引用本文的文献
1
The influence of reduced serum potassium level on the toxicity of some cardenolides in guinea pigs.血清钾水平降低对豚鼠某些强心苷毒性的影响。
Basic Res Cardiol. 1981 Jan-Feb;76(1):62-78. doi: 10.1007/BF01908163.
本文引用的文献
1
[ATTEMPT AT AN ANALYSIS OF THE RELATIONSHIP BETWEEN CHEMICAL STRUCTURE AND DIGITALIS-LIKE ACTIVITY ON THE RECEPTOR LEVEL].[关于化学结构与受体水平洋地黄样活性之间关系的分析尝试]
Arzneimittelforschung. 1964 Oct;14:1073-7.
2
Ouabain-receptor interactions in (Na+ plus K+)-ATPase preparations. IV. The molecular structure of different cardioactive steroids and other substances and their affinity to the glycoside receptor.（钠钾）-ATP酶制剂中的哇巴因-受体相互作用。IV. 不同强心甾体及其他物质的分子结构及其对糖苷受体的亲和力。
Naunyn Schmiedebergs Arch Pharmacol. 1974;283(4):335-56. doi: 10.1007/BF00501108.
3
[Pharmacology of digitalis receptors].[洋地黄受体的药理学]
Bull Acad R Med Belg. 1972;12:403-48.
4
Sensitivity to cardiac glycosides of (Na + K) ATPase prepared from human heart, guinea-pig heart and guinea-pig brain.
Arch Int Pharmacodyn Ther. 1976 Jun;221(2):339-41.
Zotero 插件