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PMID: 6094706 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Active ion transport in the renal proximal tubule. III. The ATP dependence of the Na pump.

The Journal of general physiology ·Vol. 84 ·No. 4 ·1984-10-00 ·Pages 643-62

Soltoff SP, Mandel LJ

Abstract

The dependence of the Na pump activity of intact renal tubules on the ATP concentration was investigated using a suspension of rabbit cortical tubules. Rotenone (an inhibitor of mitochondrial oxidative phosphorylation) was used in graded fashion to alter the cellular ATP, and the Na pump activity was measured when the pump was stimulated by adding KCl to tubules suspended in a K+-free medium. The K+ uptake into the tubule was measured using an extracellular K+ electrode, and the oxygen consumption (QO2) was measured using a Clark-type oxygen electrode. The Na pump activity was found to have a linear, nonsaturating dependence on the ATP concentration. However, the Na,K-ATPase hydrolytic activity (assayed biochemically) of lysed proximal tubule membranes demonstrated saturation and had a K0.5 value of 0.4 mM ATP. Presumably, unknown cytosolic factors present in the intact renal cell but not normally present in the biochemical assay accounted for the differences between the two measurements. The data suggest that an alteration in the intracellular ATP will result in a proportional change in active ion transport activity. Moreover, additional findings also suggest that the basal (non-transport-related) QO2 may be redirected to support the proximal Na pump activity when transport activity is stressed. Thus, basal respiration is not invariant under all conditions, and ion transport activity appears to be maintained foremost among cellular ATP-dependent processes.

MeSH Terms
Adenosine Triphosphate/physiology Animals Biological Transport, Active Female In Vitro Techniques Intracellular Fluid/metabolism Ion Channels/physiology Kidney Tubules, Proximal/metabolism Potassium/metabolism Rabbits Sodium/metabolism Sodium-Potassium-Exchanging ATPase/metabolism
Chemicals
Ion Channels Adenosine Triphosphate Sodium Sodium-Potassium-Exchanging ATPase Potassium
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Soltoff S P
Mandel L J
Article Info
Journal
The Journal of general physiology
Abbr.
J Gen Physiol
ISSN
0022-1295
Published
1984-10-00
Pages
643-62
Language
English
Region
United States
NLM ID
2985110R
PMCID
PMC2228754
Subset
IM
Grants
NIADDK NIH HHS · AM26816 · United States
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