Kato A, Naruse M, Knepper M A, Sands J M
Department of Medicine, Emory University School of Medicine, Atlanta, Georgia 30322, USA.
J Am Soc Nephrol. 1998 May;9(5):737-45. doi: 10.1681/ASN.V95737.
Facilitated urea transport is regulated acutely by arginine vasopressin (AVP) and hyperosmolality in rat terminal inner medullary collecting duct (IMCD). This study tested whether chronic diuresis or antidiuresis regulates facilitated urea transport. Basal and AVP-stimulated urea permeabilities (Purea) were measured in perfused IMCD subsegments. Rats were made: (1) diuretic by giving them sugar water (with or without food) or furosemide; or (2) antidiuretic by water deprivation. They were then compared with untreated rats given food and water ad libitum. Terminal IMCD from untreated rats had a high basal Purea that was significantly increased by AVP. Diuresis significantly increased basal Purea in terminal IMCD in all five diuresis protocols. Water deprivation for 1 or 3 d had no effect on basal or AVP-stimulated Purea in the IMCD2 subsegment of the terminal IMCD. In contrast, 3 d of water deprivation significantly increased both basal and AVP-stimulated Purea in the IMCD3 subsegment; 1 d of water deprivation had no effect on basal or AVP-stimulated Purea. Next, initial IMCD (IMCD1) were studied. Initial IMCD from untreated rats had a low basal Purea that was not increased by AVP (10 nM). Water diuresis (with or without food) for 3 to 5 d had no effect on basal Purea but significantly increased AVP-stimulated Purea. Furosemide diuresis and water diuresis for 1 or 7 d had no effect on either basal or AVP-stimulated Purea in initial IMCD. Water deprivation for 2 to 3 d, but not for 1 d, significantly increased basal Purea in initial IMCD, whereas water deprivation for 1 d increased AVP-stimulated Purea. It is concluded that chronic changes in hydration cause heterogeneous changes in facilitated urea transport in rat IMCD subsegments.
在大鼠终末内髓集合管(IMCD)中,易化尿素转运受精氨酸加压素(AVP)和高渗状态的急性调节。本研究检测了慢性利尿或抗利尿是否调节易化尿素转运。在灌注的IMCD亚段中测量基础和AVP刺激的尿素通透性(Purea)。将大鼠制成:(1)通过给予糖水(有或无食物)或呋塞米使其利尿;或(2)通过禁水使其抗利尿。然后将它们与随意给予食物和水的未处理大鼠进行比较。未处理大鼠的终末IMCD具有较高的基础Purea,AVP可使其显著增加。在所有五种利尿方案中,利尿均显著增加了终末IMCD的基础Purea。禁水1天或3天对终末IMCD的IMCD2亚段的基础或AVP刺激的Purea无影响。相反,禁水3天显著增加了IMCD3亚段的基础和AVP刺激的Purea;禁水1天对基础或AVP刺激的Purea无影响。接下来,研究了初始IMCD(IMCD1)。未处理大鼠的初始IMCD具有较低的基础Purea,AVP(10 nM)不能使其增加。3至5天的水利尿(有或无食物)对基础Purea无影响,但显著增加了AVP刺激的Purea。呋塞米利尿以及1天或7天的水利尿对初始IMCD的基础或AVP刺激的Purea均无影响。禁水2至3天(而非1天)显著增加了初始IMCD的基础Purea,而禁水1天增加了AVP刺激的Purea。结论是,水合状态的慢性变化导致大鼠IMCD亚段中易化尿素转运发生异质性变化。