Barlet C, Doucet A
Pflugers Arch. 1986 Jul;407(1):27-32. doi: 10.1007/BF00580716.
This study was initiated to define the dose- and time-dependence of triiodothyronine (T3) action on Na-K-ATPase in single microdissected nephron segments. For this purpose, the activity and the number of catalytic sites of Na-K-ATPase, as determined by the specific binding of 3H-ouabain, were measured following a single injection of T3 to rabbits thyroidectomized since 8-12 days. Triiodothyronine restored both the activity and the number of catalytic sites of Na-K-ATPase in a dose-dependent manner in all nephron segments where the enzyme was decreased following thyroidectomy, i.e., the proximal and the collecting tubule. At a dose of 50 micrograms/kg bw, T3 restored Na-K-ATPase activity and 3H-ouabain binding with the same kinetics. However, the kinetics depended on the nephron segments: in the proximal tubule, Na-K-ATPase stimulation occurred after a 12 h period of latency and was completed within 24 h whereas in the collecting tubule, the stimulation was biphasic with a first increase within the first 3 h and a second increase concomitantly to that observed in the proximal tubule. These results indicate that thyroid hormones regulate Na-K-ATPase activity by altering the number of catalytic sites of the enzyme. This control depends on two different mechanisms which differ by their time-dependence.
本研究旨在确定三碘甲状腺原氨酸(T3)对单个显微解剖的肾单位节段中钠钾ATP酶作用的剂量和时间依赖性。为此,在对甲状腺切除8 - 12天的兔子单次注射T3后,通过3H -哇巴因的特异性结合来测定钠钾ATP酶的活性和催化位点数量。三碘甲状腺原氨酸以剂量依赖性方式恢复了所有肾单位节段中钠钾ATP酶的活性和催化位点数量,这些节段在甲状腺切除后该酶活性降低,即近端小管和集合小管。在剂量为50微克/千克体重时,T3以相同动力学恢复钠钾ATP酶活性和3H -哇巴因结合。然而,动力学取决于肾单位节段:在近端小管中,钠钾ATP酶刺激在12小时的潜伏期后出现,并在24小时内完成;而在集合小管中,刺激是双相的,在最初3小时内有第一次增加,第二次增加与在近端小管中观察到的同时发生。这些结果表明,甲状腺激素通过改变该酶的催化位点数量来调节钠钾ATP酶活性。这种调控依赖于两种不同机制,它们在时间依赖性方面存在差异。