Hu M C, Bankir L, Michelet S, Rousselet G, Trinh-Trang-Tan M M
Service de Biologie Cellulaire, Commissariat à l'Energie Atomique, Centre d'Etudes de Saclay, Gif-sur-Yvette,and INSERM Unité 90 and INSERM Unité 367, Paris, France.
Kidney Int. 2000 Sep;58(3):1202-10. doi: 10.1046/j.1523-1755.2000.00275.x.
The facilitated urea transporters (UT), UT-A1, UT-A2, and UT-B1, are involved in intrarenal recycling of urea, an essential feature of the urinary concentrating mechanism, which is impaired in chronic renal failure (CRF). In this study, the expression of these UTs was examined in experimentally induced CRF.
The abundance of mRNA was measured by Northern analysis and that of corresponding proteins by Western blotting in rats one and five weeks after 5/6 nephrectomy (Nx).
At five weeks, urine output was enhanced threefold with a concomitant decrease in urine osmolality. The marked rise in plasma urea concentration and fall in urinary urea concentration resulted in a 30-fold decrease in the urine/plasma (U/P) urea concentration ratio, while the U/P osmoles ratio fell only fourfold. A dramatic decrease in mRNA abundance for the three UTs was observed, bringing their level at five weeks to 1/10th or less of control values. Immunoblotting showed complete disappearance of the 97 and 117 kD bands of UT-A1, and considerable reduction of UT-A2 and UT-B1 in the renal medulla. Similar, but less intense, changes were observed at one-week post-Nx. In addition to the kidney, UT-B1 is also normally expressed in brain and testis. In the brain, its mRNA expression remained normal one-week post-Nx, but decreased to about 30% of normal at five-weeks post-Nx, whereas no change was seen in testis.
(1) The decline in urinary concentrating ability seen in CRF is largely due to a major reduction of UTs involved in the process of urea concentration in the urine, while factors enabling the concentration of other solutes are less intensely affected. (2) The marked reduction of brain UT expression in CRF may be responsible for brain edema of dialysis disequilibrium syndrome observed in some patients after fast dialysis.
易化尿素转运体(UT),即UT-A1、UT-A2和UT-B1,参与肾内尿素再循环,这是尿浓缩机制的一个基本特征,而在慢性肾衰竭(CRF)中该机制受损。在本研究中,检测了这些UT在实验性诱导的CRF中的表达。
通过Northern分析测定5/6肾切除(Nx)术后1周和5周大鼠的mRNA丰度,并用Western印迹法测定相应蛋白质的丰度。
5周时,尿量增加了两倍,同时尿渗透压降低。血浆尿素浓度显著升高而尿尿素浓度降低,导致尿/血浆(U/P)尿素浓度比下降了30倍,而U/P渗透压比仅下降了4倍。观察到三种UT的mRNA丰度显著降低,使它们在5周时的水平降至对照值的1/10或更低。免疫印迹显示肾髓质中UT-A1的97和117 kD条带完全消失,UT-A2和UT-B1显著减少。在Nx术后1周观察到类似但程度较轻的变化。除肾脏外,UT-B1在脑和睾丸中也正常表达。在脑中,其mRNA表达在Nx术后1周保持正常,但在Nx术后5周降至正常水平的约30%,而在睾丸中未见变化。
(1)CRF中所见的尿浓缩能力下降主要是由于参与尿中尿素浓缩过程的UT大幅减少,而使其他溶质浓缩的因素受影响程度较轻。(2)CRF中脑UT表达的显著降低可能是一些患者在快速透析后出现透析失衡综合征脑水肿的原因。