Schiffrin E L, Intengan H D, Thibault G, Touyz R M
Clinical Research Institute of Montreal, Quebec, Canada.
Curr Opin Cardiol. 1997 Jul;12(4):354-67.
Endothelins are ubiquitously produced 21-amino-acid peptides that were discovered as an endothelial product and may play important roles in cardiovescular physiology and pathophysiology. The main endothelin produced by the endothelium is endothelin-1. The vasoconstrictor role of endothelins may participate in blood pressure elevation and vascular hypertrophy in salt-dependent models of hypertension (deoxycorticosterone acetate-salt hypertensive rats, spontaneously hypertensive rats treated with deoxycorticosterone, acetate and salt, and Dehl salt-sensitive rats), and in stroke-prone spontaneously hypertensive rats. In humans, endothelins may play important roles in moderate to severe essential hypertension, and in the hypertension of African-Americans. Endothelins may be involved in cardiac hypertrophy, and there is increasing evidence of their participation in heart failure, in which acute endothelin antagonism in humans exerts beneficial effects. Endothelin expression is enhanced in smooth muscle cells migrating into the intima of arteries in atherosclerosis, suggesting a role in atherogenesis. Endothelin may participate as a vasoconstrictor in coronary artery disease, and as a contributor to intimal proliferation in restenosis after coronary angioplasty. In patients with myocardial infarction, cardiac production of endothelin is increased, particularly in those with cardiogenic shock. There is a potential for participation of endothelins in vasospasm accompanying stroke or subarachnoid hemorrhage: in the latter, endothelin antagonism has shown beneficial effects in experimental models. In neonatal and in primary pulmonary hypertension, endothelin expression is enhanced, and in experimental models endothelin antagonism resulted in favorable responses. Systemic sclerosis is another, peripheral, form of vascular disease in which endothelin may play a role and in which endothelin antagonism may be an interesting therapeutic alternative. The pathophysiologic role of endothelins is becoming increasingly apparent in cardiovascular disease, generating interesting potential therapeutic targets for the use of endothelin antagonists or endothelin-converting enzyme inhibitors.
内皮素是普遍产生的21个氨基酸的肽,最初作为一种内皮产物被发现,可能在心血管生理和病理生理过程中发挥重要作用。内皮细胞产生的主要内皮素是内皮素-1。在盐依赖性高血压模型(醋酸脱氧皮质酮-盐高血压大鼠、用醋酸脱氧皮质酮和盐治疗的自发性高血压大鼠以及Dehl盐敏感大鼠)和易发生中风的自发性高血压大鼠中,内皮素的血管收缩作用可能参与血压升高和血管肥厚。在人类中,内皮素可能在中度至重度原发性高血压以及非裔美国人的高血压中起重要作用。内皮素可能与心脏肥厚有关,越来越多的证据表明它们参与心力衰竭,其中人类急性内皮素拮抗作用具有有益效果。在动脉粥样硬化中,迁移到动脉内膜的平滑肌细胞中内皮素表达增强,提示其在动脉粥样硬化发生过程中起作用。内皮素可能作为血管收缩剂参与冠状动脉疾病,并在冠状动脉成形术后再狭窄的内膜增殖中起作用。在心肌梗死患者中,心脏内皮素的产生增加,尤其是在心源性休克患者中。内皮素有可能参与中风或蛛网膜下腔出血伴发的血管痉挛:在后者中,内皮素拮抗作用在实验模型中已显示出有益效果。在新生儿和原发性肺动脉高压中,内皮素表达增强,在实验模型中内皮素拮抗作用产生了良好反应。系统性硬化症是另一种外周血管疾病形式,内皮素可能在其中起作用,内皮素拮抗作用可能是一种有趣的治疗选择。内皮素的病理生理作用在心血管疾病中越来越明显,为使用内皮素拮抗剂或内皮素转化酶抑制剂产生了有趣的潜在治疗靶点。