El Mernissi G, Doucet A
Pflugers Arch. 1984 Nov;402(3):258-63. doi: 10.1007/BF00585508.
Both aldosterone and dexamethasone are known to stimulate renal Na-K-ATPase activity although their action is restricted to specific nephron segments: the collecting tubule, the target site for mineralocorticoids, and the thick ascending limb and distal convoluted tubule, the target sites for glucocorticoids. As this stimulation by corticosteroids is very fast, we attempted to establish whether it occurs through de novo synthesis of new Na-K-ATPase units or by increasing the specific activity of the Na-K-ATPase units already present. For this purpose we studied the effects of aldosterone and dexamethasone on Na-K-ATPase specific activity in microdissected nephron segments from adrenalectomized rabbits. This specific activity was determined by the ratio of ATPase activity over the apparent number of catalytic units, as measured by specific 3H ouabain binding. In the proximal tubule, neither adrenalectomy nor steroid replacement altered Na-K-ATPase activity or the apparent number of catalytic sites. In other nephron segments, adrenalectomy reduced Na-K-ATPase activity and specific 3H ouabain binding concomitantly, and therefore left this enzyme's specific activity unaltered. In the cortical and outer medullary collecting tubules, 10 micrograms/kg aldosterone simultaneously restored both the activity and apparent number of catalytic units of Na-K-ATPase to their control levels, and therefore did not modify the specific activity of the pump. Conversely, 100 micrograms/kg dexamethasone increased Na-K-ATPase activity in the thick ascending limb and distal convoluted tubule without changing the apparent number of catalytic units.(ABSTRACT TRUNCATED AT 250 WORDS)
已知醛固酮和地塞米松均可刺激肾钠钾ATP酶活性,尽管它们的作用仅限于特定的肾单位节段:集合管(盐皮质激素的靶位点)以及髓袢升支粗段和远曲小管(糖皮质激素的靶位点)。由于皮质类固醇的这种刺激作用非常迅速,我们试图确定其是通过新合成钠钾ATP酶单位还是通过提高已存在的钠钾ATP酶单位的比活性来实现的。为此,我们研究了醛固酮和地塞米松对取自肾上腺切除兔子的显微解剖肾单位节段中钠钾ATP酶比活性的影响。这种比活性由ATP酶活性与通过特异性3H哇巴因结合测定的催化单位表观数量之比来确定。在近端小管中,肾上腺切除和类固醇替代均未改变钠钾ATP酶活性或催化位点的表观数量。在其他肾单位节段中,肾上腺切除同时降低了钠钾ATP酶活性和特异性3H哇巴因结合,因此该酶的比活性未改变。在皮质和外髓集合管中,10微克/千克醛固酮同时将钠钾ATP酶的活性和催化单位表观数量恢复到对照水平,因此未改变泵的比活性。相反,100微克/千克地塞米松增加了髓袢升支粗段和远曲小管中的钠钾ATP酶活性,而未改变催化单位的表观数量。(摘要截短于250词)