Tamirisa P, Frishman W H, Kumar A
Department of Medicine, Albert Einstein College of Medicine-Montefiore Medical Center, Bronx, NY 10461, USA.
Am Heart J. 1995 Sep;130(3 Pt 1):601-10. doi: 10.1016/0002-8703(95)90370-4.
Endothelin is the most potent mammalian vasoconstrictor yet discovered. Its three isoforms play leading roles in regulating vascular tone and causing mitogenesis. The isoforms bind to two major receptor subtypes (ETA and ETB), which mediate a wide variety of physiologic actions in several organ systems. Endothelin may also be a disease marker or an etiologic factor in ischemic heart disease, atherosclerosis, congestive heart failure, renal failure, myocardial and vascular wall hypertrophy, systemic hypertension, pulmonary hypertension, and subarachnoid hemorrhage. Specific and nonspecific receptor antagonists and ECE inhibitors that have been developed interfere with endothelin's function. Many available cardiovascular therapeutic agents, such as angiotensin-converting-enzyme inhibitors, calcium-entry blocking drugs, and nitroglycerin, also may interfere with endothelin release or may modify its activity. The endothelin antagonists have great potential as agents for use in the treatment of a wide spectrum of disease entities and as biologic probes for understanding the actions of endothelin in human beings.
内皮素是迄今发现的最有效的哺乳动物血管收缩剂。它的三种同工型在调节血管张力和引起有丝分裂方面起主要作用。这些同工型与两种主要的受体亚型(ETA和ETB)结合,这两种受体亚型在几个器官系统中介导多种生理作用。内皮素也可能是缺血性心脏病、动脉粥样硬化、充血性心力衰竭、肾衰竭、心肌和血管壁肥大、系统性高血压、肺动脉高压和蛛网膜下腔出血的疾病标志物或病因。已开发的特异性和非特异性受体拮抗剂以及内皮素转化酶(ECE)抑制剂会干扰内皮素的功能。许多现有的心血管治疗药物,如血管紧张素转换酶抑制剂、钙通道阻滞剂和硝酸甘油,也可能干扰内皮素的释放或改变其活性。内皮素拮抗剂作为治疗多种疾病实体的药物以及作为理解内皮素在人体内作用的生物学探针具有巨大潜力。