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PMID: 6282828 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

(Na+,K+)-ATPase kinetics within the intact renal cell. The role of oxidative metabolism.

The Journal of biological chemistry ·Vol. 257 ·No. 12 ·1982-06-25 ·Pages 6996-7002

Harris SI, Patton L, Barrett L, Mandel LJ

Abstract

The kinetics of oxygen consumption and (Na+,K+)-ATPase-mediated K+ transport was examined by reintroducing K+ into a K+-depleted suspension of renal tubules. In the presence of the substrates glucose, lactate, and alanine, a K+/O2 ratio of 10.4 +/- 0.2 was obtained, and the apparent K1/2 for K+ transport with respect to external K+ concentration was 0.9 mM. Supplementation of the substrates with the short chain fatty acid, butyric, had a 3-fold effect on the kinetic parameters examined: 1) the quantity of (Na+,K+)-ATPase-mediated ion transport per oxygen consumed fell by 17 +/- 2%; 2) the maximum rate of K+ transport increased by nearly 50%; and 3) the apparent K1/2 for transport with respect to external K+ concentration rose to 1.5 mM. These results indicate that despite decreasing the quantity of ATP produced per oxygen consumed, short chain fatty acids are able to increase the overall production of ATP during periods of high metabolic demand. The coupling between the two major metabolic processes of the renal cell, (Na+,K+)-ATPase-mediated ion transport and mitochondrial oxidative phosphorylation, is addressed in the context of these findings.

MeSH Terms
Animals Biological Transport, Active/drug effects Kidney Cortex/metabolism Kidney Tubules/metabolism Kinetics Oxygen Consumption/drug effects Potassium/metabolism,pharmacology Rabbits Sodium-Potassium-Exchanging ATPase/metabolism
Chemicals
Sodium-Potassium-Exchanging ATPase Potassium
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Harris S I
Patton L
Barrett L
Mandel L J
Article Info
Journal
The Journal of biological chemistry
Abbr.
J Biol Chem
ISSN
0021-9258
Published
1982-06-25
Pages
6996-7002
Language
English
Region
United States
NLM ID
2985121R
Subset
IM
Grants
NIADDK NIH HHS · AM-26816 · United States
NIGMS NIH HHS · GM-07171 · United States
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