Rajfer S I, Davis F R
Section of Cardiology, University of Chicago, Chicago, Ill.
Circulation. 1990 Aug;82(2 Suppl):I97-102.
The existence of two dopamine receptor subtypes (DA1 and DA2) has been firmly established. Activation of DA1 receptors is associated with vasodilation, primarily in the renal, mesenteric, cerebral, and coronary arterial beds, and a natriuresis. DA2 receptors located on postganglionic sympathetic nerves and sympathetic ganglia mediate a decrease in the release of norepinephrine from sympathetic nerve terminals. The DA receptor activity of dopamine (which activates beta 1- and alpha-adrenoceptors as well as DA receptors) plays a prominent role in determining the beneficial hemodynamic responses to this drug in patients with heart failure. As a result, recent research efforts have been directed toward the development of dopamine analogues, which are orally effective and exhibit more selective agonist activity at DA receptors. Limited clinical experience in heart failure is now available for analogues with different spectra of receptor activity than dopamine, including selective DA1 and DA2 agonists. A review of these data is presented with an attempt to define the clinical relevance of the DA receptor-agonist properties of the compounds. Although the results of early clinical studies with some of these first-generation dopamine congeners are encouraging, analysis of ongoing large-scale placebo-controlled trials will provide valuable insight into their utility as therapeutic agents for patients with heart failure.
两种多巴胺受体亚型(DA1和DA2)的存在已得到确凿证实。DA1受体的激活与血管舒张相关,主要发生在肾、肠系膜、脑和冠状动脉床,并伴有利钠作用。位于节后交感神经和交感神经节上的DA2受体介导交感神经末梢去甲肾上腺素释放的减少。多巴胺的DA受体活性(多巴胺还可激活β1和α肾上腺素能受体以及DA受体)在决定心力衰竭患者对该药有益的血流动力学反应中起重要作用。因此,最近的研究工作致力于开发多巴胺类似物,这些类似物口服有效,并且在DA受体上表现出更具选择性的激动剂活性。目前,针对与多巴胺受体活性谱不同的类似物(包括选择性DA1和DA2激动剂)在心力衰竭方面的临床经验有限。本文对这些数据进行了综述,试图确定这些化合物的DA受体激动剂特性的临床相关性。尽管早期对其中一些第一代多巴胺同系物的临床研究结果令人鼓舞,但对正在进行的大规模安慰剂对照试验的分析将为它们作为心力衰竭患者治疗药物的效用提供有价值的见解。