Department of Veterinary Pharmacology, Faculty of Agriculture, University of Miyazaki, Miyazaki 889-2192, Japan.
Cells. 2019 Feb 10;8(2):139. doi: 10.3390/cells8020139.
Aquaporin-1 (AQP1) and AQP2 are important proteins involved in the regulation of renal water handling. Both AQPs have been found in urinary extracellular vesicles (uEVs) (uEV-AQP1 and -AQP2). Cisplatin, an antineoplastic agent, is known to down-regulate renal AQP1 and AQP2. However, the effect of cisplatin on the release of uEV-AQP1 and -AQP2 is largely unknown. In this study, we examined whether treatment of rats with cisplatin affected the release of uEV-AQP1 and -AQP2. Blood tests indicated that renal function was little altered at 24 h after cisplatin treatment but thereafter decreased dramatically at all of the other time points examined. Release of uEV-AQP1 was slightly increased at 24 h and decreased at 168 h. On the other hand, release of uEV-AQP2 was decreased dramatically at 24 h, and the decrease was maintained during the experimental period. These data suggest that uEV-AQP2 can be used to detect early renal impairment due to cisplatin. Furthermore, a combination of uEV-AQP2 and -AQP1 may be useful for estimation of cisplatin-induced renal injury in a stage-dependent manner.
水通道蛋白 1(AQP1)和 AQP2 是参与肾脏水调节的重要蛋白质。两者均存在于尿细胞外囊泡(uEV)中(uEV-AQP1 和 -AQP2)。顺铂是一种抗肿瘤药物,已知可下调肾脏 AQP1 和 AQP2。然而,顺铂对 uEV-AQP1 和 -AQP2 释放的影响在很大程度上尚不清楚。在这项研究中,我们研究了顺铂处理大鼠是否会影响 uEV-AQP1 和 -AQP2 的释放。血液检测表明,顺铂治疗 24 小时后肾功能几乎没有改变,但此后在所有检查的其他时间点均显著下降。uEV-AQP1 的释放在 24 小时略有增加,而在 168 小时减少。另一方面,uEV-AQP2 的释放在 24 小时急剧下降,并且在实验期间保持下降。这些数据表明,uEV-AQP2 可用于检测顺铂引起的早期肾损伤。此外,uEV-AQP2 和 -AQP1 的组合可能有助于以阶段依赖的方式估计顺铂引起的肾损伤。