Taylor S H, Cicchetti V
University of Cardiovascular Studies, General Infirmary, Leeds, England.
Am Heart J. 1990 Dec;120(6 Pt 2):1583-90. doi: 10.1016/0002-8703(90)90063-4.
Loss of myocardial contractility, reflexly enhanced vasoconstriction, and neuroendocrine excitation are the pathophysiologic hallmarks of low-output heart failure. Drugs that counter both consequences afford considerable therapeutic potential in retarding and perhaps even in staying the consequences of the syndrome. Ibopamine possesses such potential through its unique ability to stimulate both dopaminergic- and beta-adrenoreceptors in the heart and circulatory system. Stimulation of dopaminergic- receptors and beta 2-adrenoreceptors results in vasodilatation in all regional vascular territories. beta 2-Adrenoreceptor agonist activity also affords mild positive inotropic activity in the heart, whereas stimulation of presynaptic dopaminergic- receptors (DA2) attenuates the increased sympathetic neural outflow. The drug also suppresses the renin-angiotensin-aldosterone system in addition to having a direct natriuretic activity. The pharmacodynamic effects of ibopamine, exerted through its metabolite epinine, are translated into measurable therapeutic benefits in patients with chronic heart failure. The increase in peripheral blood flow induced in all regional vascular territories, including the kidneys, is associated with increased cardiac output and stroke volume and reduction in left ventricular pressure work, wall stress, and myocardial oxygen consumption. Plasma norepinephrine, angiotensin, and aldosterone are also reduced, and renal sodium excretion is enhanced. These hemodynamic and neuroendocrine activities, which are not subject to tolerance during sustained administration of the drug, are accompanied by clinically significant improvement in symptoms, exercise tolerance, and the New York Heart Association classification of disability. More important, no proarrhythmic effects have been observed during sustained treatment, and the minimal side effects observed during long-term treatment enhance the safety profile of the drug.(ABSTRACT TRUNCATED AT 250 WORDS)
心肌收缩力丧失、反射性增强的血管收缩以及神经内分泌兴奋是低输出量心力衰竭的病理生理特征。能够对抗这两种后果的药物在延缓甚至阻止该综合征的后果方面具有相当大的治疗潜力。异波帕明具有这种潜力,因为它具有独特的能力,能够刺激心脏和循环系统中的多巴胺能受体和β肾上腺素能受体。刺激多巴胺能受体和β2肾上腺素能受体可导致所有区域血管床的血管扩张。β2肾上腺素能受体激动剂活性还能在心脏中产生轻度正性肌力作用,而刺激突触前多巴胺能受体(DA2)可减弱交感神经传出神经活动的增加。该药物除了具有直接利钠活性外,还能抑制肾素-血管紧张素-醛固酮系统。异波帕明通过其代谢产物依匹宁发挥的药效学作用,在慢性心力衰竭患者中转化为可测量的治疗益处。在包括肾脏在内的所有区域血管床中诱导的外周血流增加,与心输出量和每搏输出量增加以及左心室压力作功、壁应力和心肌氧消耗减少有关。血浆去甲肾上腺素、血管紧张素和醛固酮也会降低,肾钠排泄增加。这些血流动力学和神经内分泌活动在持续给药期间不会产生耐受性,同时伴有症状、运动耐量以及纽约心脏协会心功能分级的显著临床改善。更重要的是,在持续治疗期间未观察到促心律失常作用,长期治疗期间观察到的最小副作用提高了该药物的安全性。(摘要截短于250字)