AJP - Renal Track the topics, authors and articles important to you
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


Am J Physiol Renal Physiol 258: F1203-F1210, 1990;
0363-6127/90 $5.00
This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Lee, C. W.
Right arrow Articles by Jarvis, S. M.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Lee, C. W.
Right arrow Articles by Jarvis, S. M.

AJP - Renal Physiology, Vol 258, Issue 5 1203-F1210, Copyright © 1990 by American Physiological Society


ARTICLES

Transport characteristics of renal brush border Na(+)- and K(+)-dependent uridine carriers

C. W. Lee, C. I. Cheeseman and S. M. Jarvis
Department of Physiology, University of Alberta, Edmonton, Canada.

The uptake of uridine into rat renal brush-border membrane vesicles is mediated by Na(+)- and K(+)-dependent concentrative transport processes. At a 100 mM extravesicular cation concentration the apparent Km values were 9.7 +/- 4.2 and 28 +/- 5 microM, and Vmax values were 28 +/- 4 and 7 +/- 1 pmol.mg protein-1.s-1 for the Na(+)- and K(+)-dependent systems, respectively. Uracil, D-ribose, and D-glucose failed to inhibit the uptake processes, indicating that these carriers are specific for nucleosides. Other purines and pyrimidines inhibited uridine uptake competitively, although these two transport systems seem to favor adenosine and pyrimidines as permeants. Evidence is also given that transport is rheogenic, involving a net transfer of positive charge. The Na+:uridine and K+:uridine coupling stoichiometry was found to be 1:1 and 3:2, respectively. Both systems can also be driven by an anion gradient with apparent NO3- affinity (KNO3-) values of 42 +/- 13 and 163 +/- 54 mM for Na(+)- and K(+)-dependent systems, respectively.


This article has been cited by other articles:


Home page
Am. J. Physiol. Regul. Integr. Comp. Physiol.Home page
R. Govindarajan, A. H. Bakken, K. L. Hudkins, Y. Lai, F. J. Casado, M. Pastor-Anglada, C.-M. Tse, J. Hayashi, and J. D. Unadkat
In situ hybridization and immunolocalization of concentrative and equilibrative nucleoside transporters in the human intestine, liver, kidneys, and placenta
Am J Physiol Regulatory Integrative Comp Physiol, November 1, 2007; 293(5): R1809 - R1822.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Renal Physiol.Home page
V. L. Damaraju, A. N. Elwi, C. Hunter, P. Carpenter, C. Santos, G. M. Barron, X. Sun, S. A. Baldwin, J. D. Young, J. R. Mackey, et al.
Localization of broadly selective equilibrative and concentrative nucleoside transporters, hENT1 and hCNT3, in human kidney
Am J Physiol Renal Physiol, July 1, 2007; 293(1): F200 - F211.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Renal Physiol.Home page
L. M. Mangravite, G. Xiao, and K. M. Giacomini
Localization of human equilibrative nucleoside transporters, hENT1 and hENT2, in renal epithelial cells
Am J Physiol Renal Physiol, May 1, 2003; 284(5): F902 - F910.
[Abstract] [Full Text] [PDF]


Home page
J. Pharmacol. Exp. Ther.Home page
S. L. Borgl and a. F. E. Parkinson
Uptake and Release of [3H]Formycin B via Sodium-Dependent Nucleoside Transporters in Mouse Leukemic L1210/MA27.1 Cells
J. Pharmacol. Exp. Ther., April 1, 1997; 281(1): 347 - 353.
[Abstract] [Full Text]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Visit Other APS Journals Online