AJP - Heart Fuel your research with LabChart
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


Am J Physiol Heart Circ Physiol 248: H922-H929, 1985;
0363-6135/85 $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 Connett, R. J.
Right arrow Articles by Honig, C. R.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Connett, R. J.
Right arrow Articles by Honig, C. R.

AJP - Heart and Circulatory Physiology, Vol 248, Issue 6 922-H929, Copyright © 1985 by American Physiological Society


ARTICLES

Energy sources in fully aerobic rest-work transitions: a new role for glycolysis

R. J. Connett, T. E. Gayeski and C. R. Honig

Rate of O2 consumption (VO2), intracellular PO2, lactate extraction, and tissue contents of phosphocreatine, creatine, ATP, lactate, and pyruvate were measured during rest-work transitions in dog gracilis muscles. Samples were taken at rest and after 5, 10, 15, 30, 60, and 180 s of twitch contraction at 4/s. There was no anoxia at any time or location [companion paper, Am. J. Physiol. 248 (Heart Circ. Physiol. 17): H914-H921, 1985]. Energy was supplied by a continuous utilization of phosphocreatine stores, a slow rise in VO2, and two distinct bursts of glycolysis. Glycolytic rate was independent of tissue PO2 and VO2 and was poorly correlated with phosphocreatine under the aerobic conditions of our experiments. The glycolytic bursts served as a source of ATP, and the bulk of the lactate formed remained in the tissue. Lactate efflux was a small fraction of tissue lactate; it depended on blood flow but not on tissue lactate content. At steady state a small glycolytic flux maintained the high tissue lactate mainly by matching rates of pyruvate production and oxidation. We propose that this flux and the high tissue lactate concentration buffer cytosolic redox and/or substrate supply in support of the aerobic functions of mitochondria during exercise.


This article has been cited by other articles:


Home page
Proc. Natl. Acad. Sci. USAHome page
L. B. Gladden
Lactic acid: New roles in a new millennium
PNAS, January 16, 2001; 98(2): 395 - 397.
[Full Text] [PDF]


Home page
J. Appl. Physiol.Home page
P. A. Mole and J. J. Hoffmann
VO2 kinetics of mild exercise are altered by RER
J Appl Physiol, December 1, 1999; 87(6): 2097 - 2106.
[Abstract] [Full Text] [PDF]


Home page
J. Appl. Physiol.Home page
M. C. Hogan, R. S. Richardson, and L. J. Haseler
Human muscle performance and PCr hydrolysis with varied inspired oxygen fractions: a 31P-MRS study
J Appl Physiol, April 1, 1999; 86(4): 1367 - 1373.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Endocrinol. Metab.Home page
M. C. Hogan, E. Ingham, and S. S. Kurdak
Contraction duration affects metabolic energy cost and fatigue in skeletal muscle
Am J Physiol Endocrinol Metab, March 1, 1998; 274(3): E397 - E402.
[Abstract] [Full Text] [PDF]




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