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Am J Physiol Renal Physiol 260: F800-F805, 1991;
0363-6127/91 $5.00
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AJP - Renal Physiology, Vol 260, Issue 6 800-F805, Copyright © 1991 by American Physiological Society


ARTICLES

K(+)-ATPase-mediated Rb+ transport in rat collecting tubule: modulation during K+ deprivation

L. Cheval, C. Barlet-Bas, C. Khadouri, E. Feraille, S. Marsy and A. Doucet
Laboratoire de Physiologie Cellulaire, Unite de Recherche Associee 219, Centre National de la Recherche Scientifique, College de France, Paris.

To evaluate the involvement of K(+)-ATPase activity in K+ transport in the terminal segments of the rat nephron, we searched for the existence of a component of Rb+ uptake into microdissected segments of collecting tubule associated with the activity of this ATPase. Results indicated that K(+)-ATPase is stimulated by K+ and by Rb+ in a similar fashion and that it is specifically inhibited by the imidazopyridine Sch 28080 (apparent affinity approximately 5 x 10(-7) M). In both cortical and outer medullary collecting tubules (CCT and MCT) of normal rats, 10(-4) M Sch 28080 significantly inhibited the initial rate of Rb+ uptake. Sch 28080-sensitive Rb+ uptake in these two nephron segments was not altered by ouabain, as K(+)-ATPase activity. Finally, both K(+)-ATPase activity and Sch 28080-sensitive Rb+ uptake were increased by similar factors in the CCT and MCT of rats fed a K(+)-depleted diet for 3 days. In these two nephron segments, the apparent stoichiometry of K(+)-ATPase was 1 Rb+:1 ATP. These results demonstrate that K(+)-ATPase reflects the activity of a K+ pump that is pharmacologically similar to the gastric H(+)-K+ pump.


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