Ishikawa S, Saito T, Kasono K
Department of Medicine, Jichi Medical School Omiya Medical Center, Saitama, Japan.
J Neuroendocrinol. 2004 Apr;16(4):293-6. doi: 10.1111/j.0953-8194.2004.01177.x.
In the syndrome of inappropriate secretion of antidiuretic hormone (SIADH), inappropriately elevated secretion of vasopressin can result in a reduction of antidiuretic efficacy: a phenomenon known as 'vasopressin escape'. We compared experimental SIADH with 1-deamino-8-d-arginine vasopressin (dDAVP)-excess rats, where both groups received continuous subcutaneous administration of dDAVP by osmotic minipump but the SIADH rats also received a liquid diet that induced hyponatraemia. The SIADH rats, but not the dDAVP excess rats, showed a marked attenuation of urinary concentrating ability. Vasopressin V(2) receptor binding capacity and mRNA expression were similar between the two groups, but the SIADH rats showed a diminished up-regulation of aquaporin-2 (AQP-2) mRNA and protein expression. These findings indicate the presence of tonicity-response regions in the AQP-2 promoter gene, and that either hypervolemia or hypotonicity may attenuate the postreceptor signalling of vasopressin in renal collecting duct cells in SIADH rats.
在抗利尿激素分泌不当综合征(SIADH)中,抗利尿激素分泌不当升高可导致抗利尿作用减弱:这一现象被称为“抗利尿激素逃逸”。我们将实验性SIADH与1-去氨基-8-D-精氨酸加压素(dDAVP)过量大鼠进行了比较,两组均通过渗透微型泵持续皮下注射dDAVP,但SIADH大鼠还接受了诱导低钠血症的流食。SIADH大鼠而非dDAVP过量大鼠表现出尿浓缩能力显著减弱。两组之间加压素V(2)受体结合能力和mRNA表达相似,但SIADH大鼠水通道蛋白-2(AQP-2)mRNA和蛋白表达的上调减弱。这些发现表明AQP-2启动子基因中存在张力反应区域,并且血容量过多或低渗可能减弱SIADH大鼠肾集合管细胞中加压素的受体后信号传导。