J Physiol Wellcome Trust-funded researchers
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


J Physiol Volume 561, Number 1, 233-244, November 15, 2004 DOI: 10.1113/jphysiol.2004.069914
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Supplemental Data
Right arrow All Versions of this Article:
561/1/233    most recent
jphysiol.2004.069914v1
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 McArdle, F
Right arrow Articles by Jackson, M. J
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by McArdle, F
Right arrow Articles by Jackson, M. J

Preconditioning of skeletal muscle against contraction-induced damage: the role of adaptations to oxidants in mice

F McArdle1, S Spiers1, H Aldemir1, A Vasilaki1, A Beaver1, L Iwanejko2, A McArdle1 and M. J Jackson1

1 Department of Medicine
2 School of Biological Sciences, University of Liverpool, Liverpool L69 3GA, UK

Adaptations of skeletal muscle following exercise are accompanied by changes in gene expression, which can result in protection against subsequent potentially damaging exercise. One cellular signal activating these adaptations may be an increased production of reactive oxygen and nitrogen species (ROS). The aim of this study was to examine the effect of a short period of non-damaging contractions on the subsequent susceptibility of muscle to contraction-induced damage and to examine the changes in gene expression that occur following the initial contraction protocol. Comparisons with changes in gene expression in cultured myotubes following treatment with a non-damaging concentration of hydrogen peroxide (H2O2) were used to identify redox-sensitive genes whose expression may be modified by the increased ROS production during contractions. Hindlimb muscles of mice were subjected to a preconditioning, non-damaging isometric contraction protocol in vivo. After 4 or 12 h, extensor digitorum longus (EDL) and soleus muscles were removed and subjected to a (normally) damaging contraction protocol in vitro. Muscles were also analysed for changes in gene expression induced by the preconditioning protocol using cDNA expression techniques. In a parallel study, C2C12 myotubes were treated with a non-damaging concentration (100 µM) of H2O2 and, at 4 and 12 h following treatment, myotubes were treated with a damaging concentration of H2O2 (2 mM). Myotubes were analysed for changes in gene expression at 4 h following treatment with 100 µM H2O2 alone. Data demonstrate that a prior period of non-damaging contractile activity resulted in significant protection of EDL and soleus muscles against a normally damaging contraction protocol 4 h later. This protection was associated with significant changes in gene expression. Prior treatment of myotubes with a non-damaging concentration of H2O2 also resulted in significant protection against a damaging treatment, 4 and 12 h later. Comparison of changes in gene expression in both studies identified haem oxygenase-1 as the sole gene showing increased expression during adaptation in both instances suggesting that activation of this gene results from the increased ROS production during contractile activity and that it may play a role in protection of muscle cells against subsequent exposure to damaging activity.

(Received 11 June 2004; accepted after revision 25 August 2004; first published online 26 August 2004)
Corresponding author M. J. Jackson: Department of Medicine, University of Liverpool, Liverpool L69 3GA, UK. Email: mjj{at}liv.ac.uk




This article has been cited by other articles:


Home page
Am. J. Physiol. Regul. Integr. Comp. Physiol.Home page
D. M. Huffman, D. R. Moellering, W. E. Grizzle, C. R. Stockard, M. S. Johnson, and T. R. Nagy
Effect of exercise and calorie restriction on biomarkers of aging in mice
Am J Physiol Regulatory Integrative Comp Physiol, May 1, 2008; 294(5): R1618 - R1627.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Regul. Integr. Comp. Physiol.Home page
A. C. Kayani, G. L. Close, M. J. Jackson, and A. McArdle
Prolonged treadmill training increases HSP70 in skeletal muscle but does not affect age-related functional deficits
Am J Physiol Regulatory Integrative Comp Physiol, February 1, 2008; 294(2): R568 - R576.
[Abstract] [Full Text] [PDF]


Home page
J. Appl. Physiol.Home page
T. L. Clanton
Hypoxia-induced reactive oxygen species formation in skeletal muscle
J Appl Physiol, June 1, 2007; 102(6): 2379 - 2388.
[Abstract] [Full Text] [PDF]


Home page
J. Appl. Physiol.Home page
K. Sahlin, J. S. Nielsen, M. Mogensen, and M. Tonkonogi
Repeated static contractions increase mitochondrial vulnerability toward oxidative stress in human skeletal muscle
J Appl Physiol, September 1, 2006; 101(3): 833 - 839.
[Abstract] [Full Text] [PDF]


Home page
J. Appl. Physiol.Home page
J. P. Morton, D. P. M. MacLaren, N. T. Cable, T. Bongers, R. D. Griffiths, I. T. Campbell, L. Evans, A. Kayani, A. McArdle, and B. Drust
Time course and differential responses of the major heat shock protein families in human skeletal muscle following acute nondamaging treadmill exercise
J Appl Physiol, July 1, 2006; 101(1): 176 - 182.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Cell Physiol.Home page
T. R. Koves, R. C. Noland, A. L. Bates, S. T. Henes, D. M. Muoio, and R. N. Cortright
Subsarcolemmal and intermyofibrillar mitochondria play distinct roles in regulating skeletal muscle fatty acid metabolism
Am J Physiol Cell Physiol, May 1, 2005; 288(5): C1074 - C1082.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 2004 The Physiological Society.