Wong L L, Verbalis J G
Department of Medicine, Division of Endocrinology and Metabolism, 232 Building D, Georgetown University School of Medicine, 4000 Reservoir Road NW, Washington, DC 20007, USA.
Cardiovasc Res. 2001 Aug 15;51(3):391-402. doi: 10.1016/s0008-6363(01)00315-7.
Hyponatremia due to the syndrome of inappropriate antidiuretic hormone secretion (SIADH) and disorders of water retention such as congestive heart failure and cirrhosis is a common problem encountered in the care of the medical patient. Thus far, available treatment modalities for disorders of excess arginine vasopressin (AVP) secretion or action have been suboptimal. The development of nonpeptide AVP V2 receptor antagonists represents a promising treatment option to directly antagonize the effects of elevated plasma AVP concentrations by increasing the water permeability of renal collecting tubules, thereby promoting excretion of retained water and normalizing hypoosmolar hyponatremia. In this review, SIADH and other water retaining disorders are briefly discussed, after which the published preclinical and clinical studies in the development of several nonpeptide AVP V2 receptor antagonists are summarized. The likely therapeutic indications and potential complications of these compounds, as well as their vascular effects, are also described.
由抗利尿激素分泌不当综合征(SIADH)以及诸如充血性心力衰竭和肝硬化等水潴留性疾病导致的低钠血症,是内科患者护理中常见的问题。到目前为止,针对精氨酸加压素(AVP)分泌或作用异常的现有治疗方式并不理想。非肽类AVP V2受体拮抗剂的研发代表了一种有前景的治疗选择,可通过增加肾集合管的水通透性来直接对抗血浆AVP浓度升高的影响,从而促进潴留水分的排泄并使低渗性低钠血症恢复正常。在本综述中,将简要讨论SIADH和其他水潴留性疾病,之后总结已发表的关于几种非肽类AVP V2受体拮抗剂研发的临床前和临床研究。还将描述这些化合物可能的治疗适应症、潜在并发症及其血管效应。