Am J Physiol Cell Physiol AJP: Lung Cellular and Molecular Physiology
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


Am J Physiol Cell Physiol 256: C1273-C1276, 1989;
0363-6143/89 $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 Vemuri, R.
Right arrow Articles by Philipson, K. D.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Vemuri, R.
Right arrow Articles by Philipson, K. D.

AJP - Cell Physiology, Vol 256, Issue 6 C1273-C1276, Copyright © 1989 by American Physiological Society


ARTICLES

Ouabain treatment of cardiac cells induces enhanced Na+-Ca2+ exchange activity

R. Vemuri, S. Longoni and K. D. Philipson
Department of Medicine, University of California Los Angeles School of Medicine 90024-1760.

Inhibition of the cardiac Na+-K+-ATPase with cardiac glycosides causes a rise in internal Na+ and a subsequent increase in cellular Ca2+ due to the sarcolemmal Na+-Ca2+ exchange mechanism. We investigated the adaptation of cultured cardiac cells to prolonged elevation of internal Ca2+ after exposure to ouabain. Cultured neonatal rat heart cells were treated with 100 microM ouabain for 4-48 h. This ouabain concentration inhibited Na+-K+-ATPase activity by approximately 45% and caused modest cellular Ca2+ loading. We found that cells adapted to ouabain treatment by increasing the amount of sarcolemmal Na+-Ca2+ exchange activity by 50-90% over a 24-h period. Kinetic and immunological data indicate that the increase was due to increased numbers of functional exchangers. Neither total cellular nor total sarcolemmal protein content was affected by the ouabain treatment. These results may be relevant toward understanding the effects of therapeutic use of cardiac glycosides.


This article has been cited by other articles:


Home page
Am. J. Physiol. Cell Physiol.Home page
W. Schoner and G. Scheiner-Bobis
Endogenous and exogenous cardiac glycosides: their roles in hypertension, salt metabolism, and cell growth
Am J Physiol Cell Physiol, August 1, 2007; 293(2): C509 - C536.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Heart Circ. Physiol.Home page
C. Hurtado, M. Prociuk, T. G. Maddaford, E. Dibrov, N. Mesaeli, L. V. Hryshko, and G. N. Pierce
Cells expressing unique Na+/Ca2+ exchange (NCX1) splice variants exhibit different susceptibilities to Ca2+ overload
Am J Physiol Heart Circ Physiol, May 1, 2006; 290(5): H2155 - H2162.
[Abstract] [Full Text] [PDF]


Home page
J. Pharmacol. Exp. Ther.Home page
R. A. Walgren, J.-T. Lin, R. K.-H. Kinne, and T. Walle
Cellular Uptake of Dietary Flavonoid Quercetin 4'-beta -Glucoside by Sodium-Dependent Glucose Transporter SGLT1
J. Pharmacol. Exp. Ther., September 1, 2000; 294(3): 837 - 843.
[Abstract] [Full Text]


Home page
J. Pharmacol. Exp. Ther.Home page
L. Yu, T. Netticadan, Y.-J. Xu, V. Panagia, and N. S. Dhalla
Mechanisms of Lysophosphatidylcholine-Induced Increase in Intracellular Calcium in Rat Cardiomyocytes
J. Pharmacol. Exp. Ther., July 1, 1998; 286(1): 1 - 8.
[Abstract] [Full Text]




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