Demonstration and Characterization of two Classes of Cardiac Glycoside Binding Sites to Rat Heart Membrane Preparations Using Quantitative Computer Modeling
Author:
Publisher
Informa UK Limited
Subject
Pharmacology
Link
http://www.tandfonline.com/doi/pdf/10.3109/10799898709056779
Reference28 articles.
1. Is the cell membrane Na+, K+ -ATPase enzyme system the pharmacological receptor for digitalis?
2. Mechanism of action of therapeutic levels of cardiac glycosides
3. Evidence for two kinetically and functionally different types of cardiac glycoside receptors in the heart
4. Relation of sodium pump inhibition to positive inotropy at low concentrations of ouabain in rat heart muscle.
5. Two classes of ouabain receptors in chick ventricular cardiac cells and their relation to (Na+,K+)-ATPase inhibition, intracellular Na+ accumulation, Ca2+ influx, and cardiotonic effect.
Cited by 2 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Cardiac Electrophysiological Experiments in Numero, Part II: Models of Electrophysiological Processes;Pacing and Clinical Electrophysiology;1991-11
2. Intracellular sodium affects ouabain interaction with the Na/K pump in cultured chick cardiac myocytes.;Journal of General Physiology;1990-01-01
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