Sudo J, Morel F
Am J Physiol. 1984 May;246(5 Pt 1):C407-14. doi: 10.1152/ajpcell.1984.246.5.C407.
Na+ and K+ cell contents were measured in single pieces of tubule (0.4-0.8 mm/sample) micro-dissected from the outer medulla of collagenase-treated rat kidney tissue. Extracellular cations were washed out by rinsing the tubules in ice-cold choline-chloride solution. Na+ and K+ cell contents were measured by emission flame microphotometry after appropriate treatment of the samples. Tubular volumes were calculated from photographic pictures taken before (at 4 degrees C) and after incubation of the samples. Medullary collecting tubules (MCT) and medullary thick ascending limbs of Henle (MAL) were used in this study. When kept at 4 degrees C for 2 h or more, Na+ and K+ concentrations (meq/l cell volume) were 86.3 and 30.6, respectively, in MCT and 16.2 and 94.3, respectively, in MAL. After about 5 min of incubation at 30 degrees C, MCT samples inverted their cation contents up to new steady-state concentrations (Na+ 17.4 and K+ 97.5). During incubation, the volume of MCT samples decreased slowly and in an exponential way, the rate of which was highly temperature dependent. Na+ and K+ cell concentrations in such incubated MCT samples, however, remained fairly constant between 20 and 37 degrees C. In contrast, when MAL samples were incubated at 30 degrees C, Na+ and K+ concentrations (15.9 and 90.4, respectively) remained equal to those measured at 4 degrees C and no change in volume was observed in MAL samples.
从胶原酶处理的大鼠肾组织外髓质中显微解剖出的单段肾小管(0.4 - 0.8毫米/样本)中测量钠和钾的细胞内含量。通过在冰冷的氯化胆碱溶液中冲洗肾小管来洗去细胞外阳离子。在对样本进行适当处理后,通过发射火焰显微光度法测量钠和钾的细胞内含量。根据样本在孵育前(4℃)和孵育后拍摄的照片计算肾小管体积。本研究使用髓质集合管(MCT)和髓袢升支粗段(MAL)。当在4℃保存2小时或更长时间时,MCT中钠和钾的浓度(毫当量/细胞体积)分别为86.3和30.6,MAL中分别为16.2和94.3。在30℃孵育约5分钟后,MCT样本的阳离子含量反转至新的稳态浓度(钠17.4和钾97.5)。在孵育过程中,MCT样本的体积缓慢且呈指数下降,其速率高度依赖于温度。然而,在20至37℃之间,此类孵育的MCT样本中的钠和钾细胞浓度保持相当恒定。相比之下,当MAL样本在30℃孵育时,钠和钾的浓度(分别为15.9和90.4)与在4℃测量的浓度相等,并且在MAL样本中未观察到体积变化。