Kwon E D, Zablocki K, Jung K Y, Peters E M, García-Pérez A, Burg M B
Laboratory of Kidney and Electrolyte Metabolism, National Heart, Lung, and Blood Institute, Bethesda, Maryland 20892, USA.
Am J Physiol. 1995 Jul;269(1 Pt 1):C35-41. doi: 10.1152/ajpcell.1995.269.1.C35.
The organic osmolyte, glycerophosphocholine (GPC), accumulates in renal cells in response to high concentrations of either NaCl or urea, despite the very different effects of these solutes on cell function and volume. Together, high levels of these solutes increase GPC amount in Madin-Darby canine kidney cells by inhibiting its enzymatic degradation. The present study tests the effects of NaCl and urea, individually, on GPC accumulation and its degradation. A technique was developed to determine the absolute rate of GPC degradation by measuring the initial rate of disappearance of [3H]GPC (pulsed into the cells by hypotonic shock) and the specific activity of GPC in the cells. The mass of GPC in the cells was measured by another newly developed method, a sensitive chemiluminescent assay. We find that exposure to high NaCl or urea decreases the absolute rate of cellular GPC degradation by approximately one-half during the first 20.5 h. Reductions in GPC degradation are accompanied by commensurate decreases in the activity of GPC:choline phosphodiesterase (GPC:PDE; EC 3.1.4.2), an enzyme that catalyzes degradation of GPC. Activity of GPC:PDE falls > 50% in cells exposed for 2 h to high osmolality. Inhibition is sustained for 7 days with high urea alone. In contrast, with high NaCl alone, GPC:PDE activity reverts to control values by 7 days, by which time synthesis of GPC is increased, accounting for sustained GPC accumulation. Collectively, these data suggest that GPC accumulation in response to either high NaCl or urea occurs initially by inhibition of its degradation but that the effect of NaCl on degradation differs, in that it is transient, while that of urea is sustained.
有机渗透溶质甘油磷酸胆碱(GPC)会在肾细胞中蓄积,以应对高浓度的氯化钠(NaCl)或尿素,尽管这些溶质对细胞功能和体积的影响截然不同。这些溶质的高水平共同作用,通过抑制其酶促降解来增加Madin-Darby犬肾细胞中的GPC含量。本研究分别测试了NaCl和尿素对GPC蓄积及其降解的影响。开发了一种技术,通过测量[3H]GPC(通过低渗休克脉冲进入细胞)消失的初始速率和细胞中GPC的比活性,来确定GPC降解的绝对速率。细胞中GPC的质量通过另一种新开发的方法——灵敏的化学发光测定法进行测量。我们发现,在最初的20.5小时内,暴露于高浓度NaCl或尿素会使细胞GPC降解的绝对速率降低约一半。GPC降解的减少伴随着GPC:胆碱磷酸二酯酶(GPC:PDE;EC 3.1.4.2)活性的相应降低,该酶催化GPC的降解。暴露于高渗环境2小时的细胞中,GPC:PDE的活性下降超过50%。单独使用高浓度尿素时,抑制作用持续7天。相比之下,单独使用高浓度NaCl时,GPC:PDE活性在7天时恢复到对照值,此时GPC的合成增加,这解释了GPC的持续蓄积。总的来说,这些数据表明,响应高浓度NaCl或尿素时GPC的蓄积最初是通过抑制其降解发生的,但NaCl对降解的影响有所不同,因为它是短暂的,而尿素的影响是持续的。