Miura D S, Biedert S
J Clin Pharmacol. 1985 Oct;25(7):490-500. doi: 10.1177/009127008502500704.
Although the therapeutic actions of digitalis glycosides have been known for over 200 years, their direct inotropic actions on the heart were not established until the last 50 years. Digitalis has undergone intense research, particularly with respect to its mechanisms of action. Many authors have claimed to have found the true mechanism of action, compounding the complexity of literature. Recent subcellular studies have pointed to specific areas of action of the digitalis glycosides. Each discovery has been dependent on the greater understanding of the electrophysiologic characteristics of cardiac muscle and excitation-contraction coupling. The current hypothesis suggests that digitalis specifically inhibits Na-K ATPase. This produces an elevation in intracellular sodium level that in turn produces an increase in the intracellular calcium level. The increased quantities of calcium available to the contractile elements of cardiac muscle provide the observed increased inotropy.
尽管洋地黄糖苷的治疗作用已为人所知超过200年,但它们对心脏的直接正性肌力作用直到最近50年才得以确立。洋地黄已经历了深入研究,特别是在其作用机制方面。许多作者声称已发现其真正的作用机制,这使得文献变得更加复杂。最近的亚细胞研究已指出洋地黄糖苷的特定作用区域。每一项发现都依赖于对心肌电生理特性和兴奋-收缩偶联的更深入理解。目前的假说认为,洋地黄特异性抑制钠钾ATP酶。这会导致细胞内钠水平升高,进而使细胞内钙水平升高。可用于心肌收缩元件的钙量增加导致了观察到的正性肌力增加。