Kinetics of triiodothyronine action on Na−K-ATPase in single segments of rabbit nephron |
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Authors: | C. Barlet A. Doucet |
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Affiliation: | (1) Laboratoire de Physiologie Cellulaire, Collège de France, 11, Place Marcelin Berthelot, F-75231 Paris Cedex 05, France |
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Abstract: | 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 of3H-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 were the enzyme was decreased following thyroidectomy, i.e., the proximal and the collecting tubule. At a dose of 50 g/kg bw, T3 restored Na–K-ATPase activity and3H-ouabain binding with the same kinetics. However, the kinetics depended on the nephron segments: in the proximal tubule, Na–K-ATPase stimualtion 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 timedependence. |
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Keywords: | Na– K-ATPase Thyroidectomy Ouabain binding Single nephron segment Triiodothyronine Aldosterone |
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