Department of Nephrology, Nitobe Memorial Nakano General Hospital, Tokyo 164-8607, Japan.
Department of Nephrology, Tokyo Medical and Dental University, Tokyo 113-8519, Japan.
Int J Mol Sci. 2021 Nov 30;22(23):12950. doi: 10.3390/ijms222312950.
Ensuring the proper amount of water inside the body is essential for survival. One of the key factors in the maintenance of body water balance is water reabsorption in the collecting ducts of the kidney, a process that is regulated by aquaporin-2 (AQP2). AQP2 is a channel that is exclusively selective for water molecules and impermeable to ions or other small molecules. Impairments of AQP2 result in various water balance disorders, including nephrogenic diabetes insipidus (NDI), which is a disease characterized by a massive loss of water through the kidney and consequent severe dehydration. Dysregulation of AQP2 is also a cause of water retention with hyponatremia in heart failure, hepatic cirrhosis, and syndrome of inappropriate antidiuretic hormone secretion (SIADH). Antidiuretic hormone vasopressin is an upstream regulator of AQP2. Its binding to the vasopressin V2 receptor promotes AQP2 targeting to the apical membrane and thus enables water reabsorption. Tolvaptan, a vasopressin V2 receptor antagonist, is effective and widely used for water retention with hyponatremia. However, there are no studies showing improvement in hard outcomes or long-term prognosis. A possible reason is that vasopressin receptors have many downstream effects other than AQP2 function. It is expected that the development of drugs that directly target AQP2 may result in increased treatment specificity and effectiveness for water balance disorders. This review summarizes recent progress in studies of AQP2 and drug development challenges for water balance disorders.
确保体内有适量的水分对于生存至关重要。维持体内水平衡的关键因素之一是肾脏集合管中的水重吸收,这一过程受水通道蛋白-2(AQP2)调控。AQP2 是一种对水分子具有特异性通透性、对离子或其他小分子不可渗透的通道。AQP2 的功能障碍会导致各种水平衡紊乱,包括肾性尿崩症(NDI),其特征是大量水分通过肾脏流失,导致严重脱水。AQP2 的失调也是心力衰竭、肝硬化和抗利尿激素分泌不当综合征(SIADH)伴低钠血症时水潴留的原因。抗利尿激素血管加压素是 AQP2 的上游调节剂。它与血管加压素 V2 受体结合,促进 AQP2 靶向顶端膜,从而实现水的重吸收。托伐普坦是一种血管加压素 V2 受体拮抗剂,对低钠血症伴水潴留有效且广泛应用。然而,目前尚无研究表明其能改善硬终点或长期预后。一个可能的原因是血管加压素受体除了调控 AQP2 功能外,还有许多下游效应。预计开发直接靶向 AQP2 的药物可能会提高水平衡紊乱治疗的特异性和疗效。本文总结了 AQP2 研究及水平衡紊乱药物开发挑战的最新进展。