Schrier Robert W
University of Colorado Health Sciences Center, Denver, CO, USA.
Prog Brain Res. 2008;170:539-50. doi: 10.1016/S0079-6123(08)00441-X.
Impaired urinary dilution leading to water retention and hyponatremia may occur in patients with cardiac failure, cirrhosis, pregnancy, hypothyroidism, glucocorticoid and mineralocorticoid deficiency. The mechanisms for these defects predominantly involve the non-osmotic stimulation of arginine vasopressin release with upregulation of aquaporin 2 water channel expression and trafficking to the apical membrane of the principal cells of the collecting duct. These perturbations are reversed by V2 vasopressin receptor antagonists. In contrast, urinary concentration defects leading to polyuria are vasopressin-resistant. They may involve several factors, such as impaired counter-current concentration secondary to downregulation of Na-K-2Cl co-transporter. Vasopressin-resistant downregulation of aquaporin 2 expression has also been described as a factor in impaired urinary concentration.
心力衰竭、肝硬化、妊娠、甲状腺功能减退、糖皮质激素和盐皮质激素缺乏的患者可能会出现尿液稀释功能受损,导致水潴留和低钠血症。这些缺陷的机制主要涉及精氨酸加压素释放的非渗透性刺激,同时水通道蛋白2水通道的表达上调,并转运至集合管主细胞的顶端膜。V2加压素受体拮抗剂可逆转这些紊乱。相比之下,导致多尿的尿液浓缩功能缺陷对加压素不敏感。它们可能涉及多个因素,如钠-钾-2氯共转运体下调继发的逆流浓缩功能受损。水通道蛋白2表达的加压素抵抗性下调也被认为是尿液浓缩功能受损的一个因素。