AJP - Heart Ad Instruments
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


Am J Physiol Heart Circ Physiol 280: H318-H326, 2001;
0363-6135/01 $5.00
This Article
Right arrow Full Text
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 Web of Science
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 Web of Science (1)
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Zhang, J.
Right arrow Articles by Bache, R. J.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Zhang, J.
Right arrow Articles by Bache, R. J.
Vol. 280, Issue 1, H318-H326, January 2001

Myocardial oxygenation and high-energy phosphate levels during graded coronary hypoperfusion

Jianyi Zhang, Kamil Ugurbil, Arthur H. L. From, and Robert J. Bache

Departments of Medicine and Radiology and Center for Magnetic Resonance Research, University of Minnesota Health Sciences Center and Minneapolis Veterans Affairs Medical Center, Minneapolis, Minnesota 55455

This study was performed to determine the myocyte PO2 required to sustain normal high-energy phosphate (HEP) levels in the in vivo heart. In 10 normal dogs, myocyte PO2 values were calculated from the myocardial deoxymyoglobin resonance (Mb-delta ) intensity determined with 1H-NMR spectroscopy during sequential flow reductions produced by a hydraulic occluder that decreased coronary perfusion pressure to ~60, 50, and 40 mmHg and, finally, during total occlusion. Myocardial blood flow was measured with microspheres, and HEP levels were determined with 31P magnetic resonance spectroscopy. During control conditions, Mb-delta was undetectable. Myocardial blood flow was 1.11 ± 0.06 ml · min-1 · g-1 during basal conditions and decreased with sequential graded occlusions to 0.78 ± 0.05, 0.58 ± 0.03, and 0.38 ± 0.04 ml · min-1 · g-1, respectively; blood flow during total occlusion was 0.07 ± 0.02 ml · min-1 · g-1. Reductions of blood flow caused progressive increases of Mb-delta , which were associated with decreases of phosphocreatine (PCr), ATP, and the PCr-to-ATP ratio, as well as progressive increases of the Pi-to-PCr ratio. There was a strong linear correlation between normalized blood flow and Mb-delta (R2 = 0.89, P < 0.01). Reductions of HEP and PO2 were also highly correlated (although nonlinearly); with the assumption that myoglobin was 90% saturated with O2 during basal conditions and 5% saturated during total coronary occlusion, the intracellular PO2 values for 20% reductions of PCr and ATP were ~4.4 and ~0.9 mmHg, respectively. The data indicate that O2 availability plays an increasing role in regulation of oxidative phosphorylation when mean intracellular PO2 values fall below 5 mmHg in the in vivo heart.

myocardium; blood flow; myoglobin oxygen saturation; ischemia


This article has been cited by other articles:


Home page
J. Physiol.Home page
F. Wu, E. Y. Zhang, J. Zhang, R. J. Bache, and D. A. Beard
Phosphate metabolite concentrations and ATP hydrolysis potential in normal and ischaemic hearts
J. Physiol., September 1, 2008; 586(17): 4193 - 4208.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
M. Henrich and K. J. Buckler
Effects of Anoxia and Aglycemia on Cytosolic Calcium Regulation in Rat Sensory Neurons
J Neurophysiol, July 1, 2008; 100(1): 456 - 473.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Heart Circ. Physiol.Home page
M. N. Jameel, X. Wang, M. H. J. Eijgelshoven, A. Mansoor, and J. Zhang
Transmural distribution of metabolic abnormalities and glycolytic activity during dobutamine-induced demand ischemia
Am J Physiol Heart Circ Physiol, June 1, 2008; 294(6): H2680 - H2686.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Cell Physiol.Home page
F. Wu, J. A. L. Jeneson, and D. A. Beard
Oxidative ATP synthesis in skeletal muscle is controlled by substrate feedback
Am J Physiol Cell Physiol, January 1, 2007; 292(1): C115 - C124.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Heart Circ. Physiol.Home page
J. Zhang, G. Gong, Y. Ye, T. Guo, A. Mansoor, Q. Hu, K. Ochiai, J. Liu, X. Wang, Y. Cheng, et al.
Nitric oxide regulation of myocardial O2 consumption and HEP metabolism
Am J Physiol Heart Circ Physiol, January 1, 2005; 288(1): H310 - H316.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Heart Circ. Physiol.Home page
M. Nahrendorf, K.-H. Hiller, A. Greiser, S. Kohler, T. Neuberger, K. Hu, C. Waller, M. Albrecht, S. Neubauer, A. Haase, et al.
Chronic coronary artery stenosis induces impaired function of remote myocardium: MRI and spectroscopy study in rat
Am J Physiol Heart Circ Physiol, December 1, 2003; 285(6): H2712 - H2721.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Heart Circ. Physiol.Home page
J. Zhang, A. H. L. From, K. Ugurbil, and R. J. Bache
Myocardial oxygenation and high-energy phosphate levels during KATP channel blockade
Am J Physiol Heart Circ Physiol, October 1, 2003; 285(4): H1420 - H1427.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Heart Circ. Physiol.Home page
E. Takahashi and K. Asano
Mitochondrial respiratory control can compensate for intracellular O2 gradients in cardiomyocytes at low PO2
Am J Physiol Heart Circ Physiol, September 1, 2002; 283(3): H871 - H878.
[Abstract] [Full Text] [PDF]


Home page
Exp. Biol. Med.Home page
J. D. Tune, K. N. Richmond, M. W. Gorman, and E. O. Feigl
Control of Coronary Blood Flow during Exercise
Experimental Biology and Medicine, April 1, 2002; 227(4): 238 - 250.
[Abstract] [Full Text] [PDF]




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