Longhurst J C, Ross J
J Am Coll Cardiol. 1985 May;5(5 Suppl A):99A-105A. doi: 10.1016/s0735-1097(85)80468-x.
The administration of digitalis glycosides causes a variety of extracardiac effects. In both normal human subjects and in other species, digitalis increases smooth muscle tone of resistance and capacitance vessels. The vasoconstriction is mediated, in part, by a direct action of these glycosides on smooth muscle and, in part, by an increase in alpha-adrenergic tone. Constriction of coronary and splanchnic vessels may lead to myocardial or mesenteric ischemia. In contrast to normal subjects, patients with congestive heart failure demonstrate arteriolar and venodilation in response to these glycosides, possibly because the myocardial effect, to increase cardiac output and peripheral blood flow, overcomes the vasoconstrictor properties of these drugs. Other important actions of digitalis glycosides occur in the central and peripheral nervous systems. Their effects on the area postrema of the medulla oblongata are largely responsible for the alpha-adrenergic-mediated peripheral vasoconstriction, as well as the nausea and vomiting that frequently accompany digitalis intoxication. Actions of glycosides on the cerebral cortex are responsible for the wide range of neurotoxic effects that range from visual disturbances and headaches to seizures and coma. Finally, peripheral neurologic effects of digitalis glycosides on baroreceptor and cardiac afferent fibers may: improve the depressed function of these receptors in the situation of heart failure, and reflexly lower peripheral vascular resistance, thereby partially preventing the vascular constrictor action of these glycosides.
洋地黄糖苷的给药会引起多种心外效应。在正常人类受试者和其他物种中,洋地黄都会增加阻力血管和容量血管的平滑肌张力。这种血管收缩部分是由这些糖苷对平滑肌的直接作用介导的,部分是由α-肾上腺素能张力的增加介导的。冠状动脉和内脏血管的收缩可能导致心肌或肠系膜缺血。与正常受试者不同,充血性心力衰竭患者对这些糖苷会表现出小动脉和静脉扩张,这可能是因为增加心输出量和外周血流量的心肌效应克服了这些药物的血管收缩特性。洋地黄糖苷的其他重要作用发生在中枢和外周神经系统。它们对延髓最后区的作用在很大程度上导致了α-肾上腺素能介导的外周血管收缩,以及洋地黄中毒时经常伴随的恶心和呕吐。糖苷对大脑皮层的作用导致了从视觉障碍、头痛到癫痫发作和昏迷等广泛的神经毒性效应。最后,洋地黄糖苷对压力感受器和心脏传入纤维的外周神经效应可能:在心力衰竭的情况下改善这些感受器的功能障碍,并反射性降低外周血管阻力,从而部分防止这些糖苷的血管收缩作用。