Haynes W G, Webb D J
Department of Internal Medicine, University of Iowa, Iowa City, USA.
J Hypertens. 1998 Aug;16(8):1081-98. doi: 10.1097/00004872-199816080-00001.
The endothelins are a family of endothelium-derived peptides that possess characteristically sustained vasoconstrictor properties. Endothelin-1 appears to be the predominant member of the family generated by vascular endothelial cells. In addition to its direct vascular effects, endothelin-1 has inotropic and mitogenic properties, influences homeostasis of salt and water, alters central and peripheral sympathetic activity and stimulates the renin-angiotensin-aldosterone system. Studies with endothelin receptor antagonists have indicated that endothelin-1 probably has complex opposing vascular effects mediated through vascular smooth muscle and endothelial ET(A) and ET(B)receptors. Endogenous generation of endothelin-1 appears to contribute to maintenance of basal vascular tone and blood pressure through activation of vascular smooth muscle ET(A)receptors. At the same time, endogenous endothelin-1 acts through endothelial ET(B) receptors to stimulate formation of nitric oxide tonically and to oppose vasoconstriction. In view of the multiple cardiovascular actions of endothelin-1, there has been much interest in its contribution to the pathophysiology of hypertension. Results of most studies suggest that generation of, or sensitivity to, endothelin-1 is no greater in hypertensive than it is in normotensive subjects. Nonetheless, the deleterious vascular effects of endogenous endothelin-1 may be accentuated by reduced generation of nitric oxide caused by hypertensive endothelial dysfunction. It also appears likely that endothelin participates in the adverse cardiac and vascular remodelling of hypertension, as well as in hypertensive renal damage. Irrespective of whether vascular endothelin activity is increased in hypertension, anti-endothelin agents do produce vasodilatation and lower blood pressure in hypertensive humans. There is more persuasive evidence for increased endothelin-1 activity in secondary forms of hypertension, including pre-eclampsia and renal hypertension. Endothelin-1 also appears to play an important role in pulmonary hypertension, both primary and secondary to diseases such as chronic heart failure. The hypotensive effects of endothelin converting enzyme inhibitors and endothelin receptor antagonists should be useful in the treatment of hypertension and related diseases. Development of such agents will increase knowledge of the physiological and pathological roles of the endothelins, and should generate drugs with novel benefits.
内皮素是一族由内皮细胞产生的肽类物质,具有典型的持续血管收缩特性。内皮素-1似乎是血管内皮细胞产生的该家族中的主要成员。除了直接的血管效应外,内皮素-1还具有变力性和促有丝分裂特性,影响盐和水的稳态,改变中枢和外周交感神经活动,并刺激肾素-血管紧张素-醛固酮系统。内皮素受体拮抗剂的研究表明,内皮素-1可能通过血管平滑肌以及内皮ET(A)和ET(B)受体介导复杂的相反血管效应。内皮素-1的内源性生成似乎通过激活血管平滑肌ET(A)受体来维持基础血管张力和血压。同时,内源性内皮素-1通过内皮ET(B)受体发挥作用,持续刺激一氧化氮的形成并对抗血管收缩。鉴于内皮素-1的多种心血管作用,人们对其在高血压病理生理学中的作用非常感兴趣。大多数研究结果表明,高血压患者中内皮素-1的生成或对其的敏感性并不比血压正常者更高。尽管如此,高血压性内皮功能障碍导致的一氧化氮生成减少可能会加剧内源性内皮素-1的有害血管效应。内皮素似乎也参与了高血压的不良心脏和血管重塑以及高血压性肾损害。无论高血压时血管内皮素活性是否增加,抗内皮素药物确实能使高血压患者血管舒张并降低血压。有更具说服力的证据表明,在包括先兆子痫和肾性高血压在内的继发性高血压形式中,内皮素-1活性增加。内皮素-1在原发性和继发于慢性心力衰竭等疾病的肺动脉高压中似乎也起重要作用。内皮素转换酶抑制剂和内皮素受体拮抗剂的降压作用应有助于治疗高血压及相关疾病。开发此类药物将增加对内皮素生理和病理作用的了解,并应产生具有新益处的药物。