Rosenthal Stephen M, Feldman Brian J, Vargas Gabriel A, Gitelman Stephen E
University of California, San Francisco.
Pediatr Endocrinol Rev. 2006 Dec;4 Suppl 1:66-70.
Mutations of G protein-coupled receptors are responsible for a wide range of diseases. With respect to water balance and vasopressin signaling, more than 180 different inactivating mutations have been previously described in the V2 vasopressin receptor (V2R), resulting in nephrogenic diabetes insipidus. In contrast, we have recently described the first known patients with V2R activating mutations. Patients with these novel gain-of-function V2R mutations have a disorder which we have termed "nephrogenic syndrome of inappropriate antidiuresis" (NSIAD): a clinical presentation consistent with the syndrome of inappropriate antidiuretic hormone secretion but with undetectable levels of arginine vasopressin (antidiuretic hormone). The mechanisms by which these mutations constitutively activate the V2R are currently being investigated.
G蛋白偶联受体的突变与多种疾病有关。在水平衡和血管加压素信号传导方面,先前已在V2血管加压素受体(V2R)中描述了180多种不同的失活突变,导致肾性尿崩症。相比之下,我们最近描述了首例已知的具有V2R激活突变的患者。患有这些新型功能获得性V2R突变的患者患有一种我们称为“不适当抗利尿激素分泌性肾性综合征”(NSIAD)的疾病:一种临床表现与抗利尿激素分泌不适当综合征一致,但精氨酸血管加压素(抗利尿激素)水平检测不到的疾病。目前正在研究这些突变组成性激活V2R的机制。