Rai T, Sekine K, Kanno K, Hata K, Miura M, Mizushima A, Marumo F, Sasaki S
Second Department of Internal Medicine, Tokyo Medical and Dental University, Japan.
J Am Soc Nephrol. 1997 Sep;8(9):1357-62. doi: 10.1681/ASN.V891357.
Previous studies by the authors demonstrated that the response of urinary aquaporin-2 (AQP2) excretion to dDAVP (deamino-8-D-arginine vasopressin) infusion is an index of vasopressin action on the kidney (N Engl J Med 332: 1540-1545, 1995). In the study presented here, the characteristics of urinary excretion of AQP2 were examined further. An RIA suitable for AQP2 in the urine was established. Relatively high concentrations of detergent and bovine serum albumin in the RIA buffer allowed analysis of urine samples with a wide range of concentrations and increased the sensitivity of the assay. AQP2 in the urine existed as a high molecular weight form of approximately 190 kD by HPLC analysis. The mean urinary AQP2 concentration corrected for creatinine in spot urine samples of healthy subjects who voided in the morning was 1081 +/- 699 fmol/mg creatinine (mean +/- SD, n = 208). The amount of daily excretion of AQP2 in the urine was the same in men and women. Urinary AQP2 content was not affected by age of the subjects and showed a positive correlation with urine osmolality. Finally, the fraction of AQP2 excreted in the urine compared with whole kidney content was determined in the rat. Approximately 3% of AQP2 in the kidney was excreted daily, and this fraction did not change when rats were dehydrated for 3 d. These data demonstrate the necessity of establishing well-designed protocols to use urinary AQP2 as a marker of AVP action.
作者之前的研究表明,尿水通道蛋白-2(AQP2)排泄对去氨加压素(dDAVP)输注的反应是血管加压素对肾脏作用的一个指标(《新英格兰医学杂志》332: 1540 - 1545, 1995)。在本文所呈现的研究中,对AQP2的尿排泄特征进行了进一步研究。建立了一种适用于尿液中AQP2的放射免疫分析方法。放射免疫分析缓冲液中相对高浓度的去污剂和牛血清白蛋白使得能够分析浓度范围广泛的尿液样本,并提高了检测的灵敏度。通过高效液相色谱分析,尿液中的AQP2以大约190 kD的高分子量形式存在。早晨排尿的健康受试者即时尿样中经肌酐校正后的平均尿AQP2浓度为1081 +/- 699 fmol/mg肌酐(平均值 +/- 标准差,n = 208)。尿液中AQP2的每日排泄量在男性和女性中相同。尿AQP2含量不受受试者年龄的影响,并且与尿渗透压呈正相关。最后,在大鼠中测定了尿液中排泄的AQP2与整个肾脏含量相比的比例。肾脏中约3%的AQP2每日被排泄,并且当大鼠脱水3天时,这一比例没有变化。这些数据表明有必要建立精心设计的方案,以便将尿AQP2用作血管加压素作用的标志物。