Am J Physiol Cell Physiol AJP: Advances in Physiology Education
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


Am J Physiol Cell Physiol 290: C1199-C1208, 2006. First published November 23, 2005; doi:10.1152/ajpcell.00469.2005
0363-6143/06 $8.00
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
290/4/C1199    most recent
00469.2005v1
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 ISI Web of Science (11)
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Verburg, E.
Right arrow Articles by Lamb, G. D.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Verburg, E.
Right arrow Articles by Lamb, G. D.

MUSCLE CELL BIOLOGY AND CELL MOTILITY

Long-lasting muscle fatigue: partial disruption of excitation-contraction coupling by elevated cytosolic Ca2+ concentration during contractions

Esther Verburg, Travis L. Dutka, and Graham D. Lamb

Department of Zoology, La Trobe University, Bundoora Campus, Melbourne, Victoria, Australia

Submitted 20 September 2005 ; accepted in final form 17 November 2005

The repeated elevation of cytosolic Ca2+ concentration ([Ca2+]i) above resting levels during contractile activity has been associated with long-lasting muscle fatigue. The mechanism underlying this fatigue appears to involve elevated [Ca2+]i levels that induce disruption of the excitation-contraction (E-C) coupling process at the triad junction. Unclear, however, are which aspects of the activity-related [Ca2+]i changes are responsible for the deleterious effects, in particular whether they depend primarily on the peak [Ca2+]i reached locally at particular sites or on the temporal summation of the increased [Ca2+] in the cytoplasm as a whole. In this study, we used mechanically skinned fibers from rat extensor digitorum longus muscle, in which the normal E-C coupling process remains intact. The [Ca2+]i was raised either by applying a set elevated [Ca2+] throughout the fiber or by using action potential stimulation to induce the release of sarcoplasmic reticulum Ca2+ by the normal E-C coupling system with or without augmentation by caffeine or buffering with BAPTA. Herein we show that elevating [Ca2+]i in the physiological range of 2–20 µM irreversibly disrupts E-C coupling in a concentration-dependent manner but requires exposure for a relatively long time (1–3 min) to cause substantial uncoupling. The effectiveness of Ca2+ released via the endogenous system in disrupting E-C coupling indicates that the relatively high [Ca2+]i attained close to the release site at the triad junction is a more important factor than the increase in bulk [Ca2+]i. Our results suggest that during prolonged vigorous activity, the many repeated episodes of relatively high triadic [Ca2+] can disrupt E-C coupling and lead to long-lasting fatigue.

skeletal muscle; low-frequency fatigue; ryanodine receptor; skinned fiber



Address for reprint requests and other correspondence: E. Verburg, Dept. of Zoology, La Trobe Univ., Bundoora Campus, Melbourne, Victoria 3086, Australia (e-mail: e.verburg{at}latrobe.edu.au)




This article has been cited by other articles:


Home page
J. Physiol.Home page
R. M. Murphy, T. L. Dutka, and G. D. Lamb
Hydroxyl radical and glutathione interactions alter calcium sensitivity and maximum force of the contractile apparatus in rat skeletal muscle fibres
J. Physiol., April 15, 2008; 586(8): 2203 - 2216.
[Abstract] [Full Text] [PDF]


Home page
J. Physiol.Home page
T. L. Dutka, R. M. Murphy, D. G. Stephenson, and G. D. Lamb
Chloride conductance in the transverse tubular system of rat skeletal muscle fibres: importance in excitation-contraction coupling and fatigue
J. Physiol., February 1, 2008; 586(3): 875 - 887.
[Abstract] [Full Text] [PDF]


Home page
Physiol. Rev.Home page
D. G. Allen, G. D. Lamb, and H. Westerblad
Skeletal Muscle Fatigue: Cellular Mechanisms
Physiol Rev, January 1, 2008; 88(1): 287 - 332.
[Abstract] [Full Text] [PDF]


Home page
J. Appl. Physiol.Home page
D. G. Allen, G. D. Lamb, and H. Westerblad
Impaired calcium release during fatigue
J Appl Physiol, January 1, 2008; 104(1): 296 - 305.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Cell Physiol.Home page
T. L. Dutka and G. D. Lamb
Na+-K+ pumps in the transverse tubular system of skeletal muscle fibers preferentially use ATP from glycolysis
Am J Physiol Cell Physiol, September 1, 2007; 293(3): C967 - C977.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Cell Physiol.Home page
T. L. Dutka and G. D. Lamb
Transverse tubular system depolarization reduces tetanic force in rat skeletal muscle fibers by impairing action potential repriming
Am J Physiol Cell Physiol, June 1, 2007; 292(6): C2112 - C2121.
[Abstract] [Full Text] [PDF]


Home page
J. Physiol.Home page
R. M. Murphy, E. Verburg, and G. D. Lamb
Ca2+ activation of diffusible and bound pools of {micro}-calpain in rat skeletal muscle
J. Physiol., October 15, 2006; 576(2): 595 - 612.
[Abstract] [Full Text] [PDF]


Home page
J. Appl. Physiol.Home page
G. D. Lamb and D. G. Stephenson
The Last Word: Point:Counterpoint authors respond to commentaries on "Lactic acid accumulation is an advantage/disadvantage during muscle activity"
J Appl Physiol, July 1, 2006; 101(1): 369 - 369.
[Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Visit Other APS Journals Online
Copyright © 2006 by the American Physiological Society.