spacer gif spacer gif spacer gif spacer gif spacer gif
 QUICK SEARCH:   [advanced]


spacer gif
     Home     Help     Feedback     Subscriptions     Archive     Search     Table of Contents    

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
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Goldspink, D. F.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Goldspink, D. F.

Journal of Experimental Biology, Vol 160, Issue 1 127-148, Copyright © 1991 by Company of Biologists


JOURNAL ARTICLES

Exercise-related changes in protein turnover in mammalian striated muscle

DF Goldspink
Department of Cardiovascular Studies, University of Leeds, UK.

Contractile activity is an important determinant of the size, rate of protein turnover and phenotypic properties of muscle. Animal models that decrease muscle activity invariably accelerate the rate of protein degradation, usually complementing decreases in the rate of protein synthesis. The net effect is muscle atrophy. By contrast, increased activity and/or passive stretch enhance the synthesis of new proteins, whilst protein catabolism may be either decreased or increased. Muscle hypertrophy results. Endurance activities in man and animals usually induce cardiac hypertrophy, and increased fatigue resistance in skeletal muscle. During exercise the whole body and its skeletal musculature exhibit a negative nitrogen balance, and there is general agreement that rates of protein synthesis are decreased. Changes in protein degradation are, however, much less clearly defined. Resistance exercises induce the opposite changes, with the size of the heart remaining unchanged whilst the bulk and strength of skeletal muscle increase. No real consensus currently exists about the nature of the changes in protein turnover with this type of exercise. More carefully designed and executed experiments are required.


This article has been cited by other articles:


Home page
J. Appl. Physiol.Home page
G. N. Askew, V. M. Cox, J. D. Altringham, and D. F. Goldspink
Mechanical properties of the latissimus dorsi muscle after cyclic training
J Appl Physiol, August 1, 2002; 93(2): 649 - 659.
[Abstract] [Full Text] [PDF]


Home page
J. Exp. Biol.Home page
C. G. Guglielmo, T. Piersma, and T. D. Williams
A sport-physiological perspective on bird migration: evidence for flight-induced muscle damage
J. Exp. Biol., January 8, 2001; 204(15): 2683 - 2690.
[Abstract] [Full Text] [PDF]


Home page
J. Exp. Biol.Home page
A Lindstrom, A Kvist, T Piersma, A Dekinga, and M. Dietz
Avian pectoral muscle size rapidly tracks body mass changes during flight, fasting and fuelling
J. Exp. Biol., January 3, 2000; 203(5): 913 - 919.
[Abstract] [PDF]


Home page
J. Exp. Biol.Home page
M. Dietz, T Piersma, and A Dekinga
Body-building without power training: endogenously regulated pectoral muscle hypertrophy in confined shorebirds
J. Exp. Biol., January 10, 1999; 202(20): 2831 - 2837.
[Abstract] [PDF]


Home page
J. Appl. Physiol.Home page
K. D. Tipton, A. A. Ferrando, B. D. Williams, and R. R. Wolfe
Muscle protein metabolism in female swimmers after a combination of resistance and endurance exercise
J Appl Physiol, November 1, 1996; 81(5): 2034 - 2038.
[Abstract] [Full Text] [PDF]




© The Company of Biologists Ltd 1991