J Physiol Society Membership
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


J Physiol Volume 544, Number 3, 765-776, November 1, 2002 DOI: 10.1113/jphysiol.2002.024968
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
544/3/765    most recent
2002.024968v1
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 Poel, C. v. d.
Right arrow Articles by Stephenson, D. G.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Poel, C. v. d.
Right arrow Articles by Stephenson, D. G.
Journal of Physiology (2002), 544.3, pp. 765-776
© Copyright 2002 The Physiological Society
DOI: 10.1113/jphysiol.2002.024968

Reversible changes in Ca2+-activation properties of rat skeletal muscle exposed to elevated physiological temperatures

Chris van der Poel and D. George Stephenson

Department of Zoology, La Trobe University, Bundoora, Victoria 3086, Australia

Exposure of relaxed rat extensor digitorum longus (EDL; predominantly fast-twitch) muscle to temperatures in the upper physiological range for mammalian skeletal muscle (43-46 °C) led to reversible alterations of the contractile activation properties. These properties were studied using the mechanically skinned fibre preparation activated in Ca2+-buffered solutions. The maximum Ca2+-activated force (maximum force per cross-sectional area) and the steepness of force-pCa (-log10[Ca2+]) curves as measured by the Hill coefficient (nH) reversibly decreased by factors of 8 and 2.5, respectively, when the EDL muscle was treated at 43 °C for 30 min and 5 and 2.8, respectively, with treatment at 46 °C for 5 min. Treatment at 47 °C for 5 min produced an even more marked depression in maximum specific force, which fully recovered after treatment, and in the Hill coefficient, which did not recover after treatment. After all temperature treatments there was no change in the level of [Ca2+] at which 50 % maximum force was generated. The temperature-induced depression in force production and steepness of the force-pCa curves were shown to be associated with superoxide (O2-) production in muscle (apparent rate of O2- production at room temperature, 0.055 ± 0.008 nmol min-1 (g wet weight)-1; and following treatment to 46 °C for 5 min, 1.8 ± 0.2 nmol min-1 (g wet weight)-1) because 20 mM Tiron, a membrane-permeant O2- scavenger, was able to markedly suppress the net rate of O2- production and prevent any temperature-induced depression of contractile parameters. The temperature-induced depression in force production of the contractile apparatus could be reversed either by allowing the intact muscle to recover for 3-4 h at room temperature or by treatment of the skinned fibre preparation with dithiothreitol (a potent reducing agent) in the relaxing solution. These results demonstrate that mammalian skeletal muscle has the ability to uncouple force production reversibly from the activator Ca2+ as the temperature increases in the upper physiological range through an increase in O2- production.



This article has been cited by other articles:


Home page
Mol. Biol. CellHome page
N. Vlahovich, A. J. Kee, C. Van der Poel, E. Kettle, D. Hernandez-Deviez, C. Lucas, G. S. Lynch, R. G. Parton, P. W. Gunning, and E. C. Hardeman
Cytoskeletal Tropomyosin Tm5NM1 Is Required for Normal Excitation-Contraction Coupling in Skeletal Muscle
Mol. Biol. Cell, January 1, 2009; 20(1): 400 - 409.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Regul. Integr. Comp. Physiol.Home page
S. R. Oliver, V. P. Wright, N. Parinandi, and T. L. Clanton
Thermal tolerance of contractile function in oxidative skeletal muscle: no protection by antioxidants and reduced tolerance with eicosanoid enzyme inhibition
Am J Physiol Regulatory Integrative Comp Physiol, November 1, 2008; 295(5): R1695 - R1705.
[Abstract] [Full Text] [PDF]


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
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
Am. J. Physiol. Cell Physiol.Home page
J. D. Schertzer, C. v. d. Poel, T. Shavlakadze, M. D. Grounds, and G. S. Lynch
Muscle-specific overexpression of IGF-I improves E-C coupling in skeletal muscle fibers from dystrophic mdx mice
Am J Physiol Cell Physiol, January 1, 2008; 294(1): C161 - C168.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Cell Physiol.Home page
J. N. Edwards, W. A. Macdonald, C. van der Poel, and D. G. Stephenson
O2bullet production at 37{degrees}C plays a critical role in depressing tetanic force of isolated rat and mouse skeletal muscle
Am J Physiol Cell Physiol, August 1, 2007; 293(2): C650 - C660.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Cell Physiol.Home page
C. van der Poel and D. G. Stephenson
Effects of elevated physiological temperatures on sarcoplasmic reticulum function in mechanically skinned muscle fibers of the rat
Am J Physiol Cell Physiol, July 1, 2007; 293(1): C133 - C141.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Cell Physiol.Home page
C. van der Poel, J. N. Edwards, W. A. Macdonald, and D. G. Stephenson
Mitochondrial superoxide production in skeletal muscle fibers of the rat and decreased fiber excitability
Am J Physiol Cell Physiol, April 1, 2007; 292(4): C1353 - C1360.
[Abstract] [Full Text] [PDF]


Home page
J. Physiol.Home page
W. A. Macdonald and D. G. Stephenson
Effect of ADP on slow-twitch muscle fibres of the rat: implications for muscle fatigue
J. Physiol., May 15, 2006; 573(1): 187 - 198.
[Abstract] [Full Text] [PDF]


Home page
J. Physiol.Home page
T. R. Moopanar and D. G. Allen
The activity-induced reduction of myofibrillar Ca2+ sensitivity in mouse skeletal muscle is reversed by dithiothreitol
J. Physiol., February 15, 2006; 571(1): 191 - 200.
[Abstract] [Full Text] [PDF]


Home page
J. Physiol.Home page
T. R Moopanar and D. G Allen
Reactive oxygen species reduce myofibrillar Ca2+ sensitivity in fatiguing mouse skeletal muscle at 37{degrees}C
J. Physiol., April 1, 2005; 564(1): 189 - 199.
[Abstract] [Full Text] [PDF]


Home page
J. Appl. Physiol.Home page
J. A. Leppik, R. J. Aughey, I. Medved, I. Fairweather, M. F. Carey, and M. J. McKenna
Prolonged exercise to fatigue in humans impairs skeletal muscle Na+-K+-ATPase activity, sarcoplasmic reticulum Ca2+ release, and Ca2+ uptake
J Appl Physiol, October 1, 2004; 97(4): 1414 - 1423.
[Abstract] [Full Text] [PDF]


Home page
J. Physiol.Home page
W. A. Macdonald and D. G. Stephenson
Effects of ADP on action potential-induced force responses in mechanically skinned rat fast-twitch fibres
J. Physiol., September 1, 2004; 559(2): 433 - 447.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 2002 The Physiological Society.