Lee S M, Chekal M A, Katz A I
Am J Physiol. 1983 May;244(5):F504-9. doi: 10.1152/ajprenal.1983.244.5.F504.
Glucocorticoids influence numerous kidney functions but the precise location of glucocorticoid receptors in the nephron is not known. To identify the renal binding sites of corticosterone, the natural glucocorticoid in the rat, we measured the binding of [3H]corticosterone to discrete nephron segments microdissected from adrenalectomized rats. Highest specific binding capacity at 25 degrees C (expressed as fmol X cm-1 +/- SE) was found in the cortical collecting tubule (9.69 +/- 0.77) followed in decreasing order by the distal convoluted tubule (2.70 +/- 0.49), medullary collecting tubule (2.58 +/- 0.64), proximal convoluted tubule (1.09 +/- 0.10), and pars recta (0.57 +/- 0.08). Binding was lowest in the thick ascending limb of Henle's loop, with comparable values in the medullary (0.27 +/- 0.05) and cortical (0.26 +/- 0.05) portions of this segment. The apparent maximal binding capacity of the cortical collecting tubule for corticosterone exceeded by nearly two orders of magnitude that of aldosterone previously measured by us in this structure, which is in agreement with the observations of other investigators in kidney cytosol. Specific binding of corticosterone can be demonstrated along the entire rat nephron, but binding sites are concentrated in the cortical collecting tubule. This segment appears to be the main target site for corticosterone as it is for aldosterone.
糖皮质激素影响众多肾脏功能,但糖皮质激素受体在肾单位中的精确位置尚不清楚。为了确定大鼠体内天然糖皮质激素皮质酮在肾脏的结合位点,我们测量了[3H]皮质酮与从肾上腺切除大鼠身上显微解剖得到的离散肾单位节段的结合情况。在25摄氏度时,皮质集合管的特异性结合能力最高(以fmol X cm-1 +/- SE表示),为(9.69 +/- 0.77),随后依次为远曲小管(2.70 +/- 0.49)、髓质集合管(2.58 +/- 0.64)、近曲小管(1.09 +/- 0.10)和直部(0.57 +/- 0.08)。亨氏袢厚壁升支的结合能力最低,该节段髓质部分(0.27 +/- 0.05)和皮质部分(0.26 +/- 0.05)的结合能力相当。皮质集合管对皮质酮的表观最大结合能力比我们之前在此结构中测得的醛固酮的结合能力高出近两个数量级,这与其他研究者在肾细胞溶胶中的观察结果一致。皮质酮的特异性结合在整个大鼠肾单位中均可显示,但结合位点集中在皮质集合管。该节段似乎是皮质酮的主要靶位点,就如同它是醛固酮的主要靶位点一样。