Am J Physiol Cell Physiol Fuel your research with LabChart
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


Am J Physiol Cell Physiol 264: C1259-C1269, 1993;
0363-6143/93 $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
Right arrow Citation Map
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 Koss, K. L.
Right arrow Articles by Grubbs, R. D.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Koss, K. L.
Right arrow Articles by Grubbs, R. D.

AJP - Cell Physiology, Vol 264, Issue 5 C1259-C1269, Copyright © 1993 by American Physiological Society


ARTICLES

Mg2+ buffering in cultured chick ventricular myocytes: quantitation and modulation by Ca2+

K. L. Koss, R. W. Putnam and R. D. Grubbs
Department of Pharmacology and Toxicology, School of Medicine, Wright State University, Dayton, Ohio 45435.

To characterize the Mg2+ buffering of cultured chick ventricular myocytes, cytosolic Mg2+ was increased by liberating Mg2+ normally chelated by ATP upon total depletion of ATP content. Because the total Mg content and cell volume remained constant during this time, the difference between the amount of Mg2+ liberated (2.7 mM) and the 0.9 mM increase in cytosolic Mg2+ activity measured fluorometrically with mag-fura-2 indicates a sizable Mg2+ buffering. A new term, the Mg2+ buffer coefficient (BMg), was derived to quantify this buffering. We also determined that cytosolic Mg2+ activity increased by only 0.6 mM in cells acutely exposed to zero external Ca2+ during ATP depletion. In the absence of extracellular Ca2+, the basal cytosolic Ca2+ activity (alpha Ca2+i) was reduced by 72%, whereas the increase in alpha Ca2+i induced by ATP depletion was substantially blunted; no difference in either the time course of adenine nucleotide changes or the Ca and Mg content was observed. The BMg value calculated for these cells indicates that Mg2+ buffering is substantially greater in the absence of extracellular Ca2+ (2.5) than when extracellular Ca2+ is present (1.4), indicating that alpha Ca2+i affects cytosolic Mg2+ activity in ventricular myocytes. Therefore the Mg2+ buffering of ventricular myocytes appears to be comprised of at least two components: 1) a Ca(2+)-insensitive adenine nucleotide pool and 2) a Ca(2+)-sensitive nonadenine nucleotide pool.


This article has been cited by other articles:


Home page
Am. J. Physiol. Cell Physiol.Home page
M. Henrich and K. J. Buckler
Effects of anoxia, aglycemia, and acidosis on cytosolic Mg2+, ATP, and pH in rat sensory neurons
Am J Physiol Cell Physiol, January 1, 2008; 294(1): C280 - C294.
[Abstract] [Full Text] [PDF]


Home page
J. Bacteriol.Home page
K. M. Papp and M. E. Maguire
The CorA Mg2+ Transporter Does Not Transport Fe2+
J. Bacteriol., November 15, 2004; 186(22): 7653 - 7658.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Heart Circ. Physiol.Home page
M. N. Sharikabad, K. M. Ostbye, and O. Brors
Increased [Mg2+]o reduces Ca2+ influx and disruption of mitochondrial membrane potential during reoxygenation
Am J Physiol Heart Circ Physiol, November 1, 2001; 281(5): H2113 - H2123.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Gastrointest. Liver Physiol.Home page
T. E. Fagan and A. Romani
{alpha}1-Adrenoceptor-induced Mg2+ extrusion from rat hepatocytes occurs via Na+-dependent transport mechanism
Am J Physiol Gastrointest Liver Physiol, June 1, 2001; 280(6): G1145 - G1156.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Cell Physiol.Home page
M. Tashiro and M. Konishi
Sodium gradient-dependent transport of magnesium in rat ventricular myocytes
Am J Physiol Cell Physiol, December 1, 2000; 279(6): C1955 - C1962.
[Abstract] [Full Text] [PDF]




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