AJP - Regu Journal of Neurophysiology
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


Am J Physiol Regul Integr Comp Physiol 290: R393-R404, 2006. First published September 22, 2005; doi:10.1152/ajpregu.00006.2005
0363-6119/06 $8.00
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
290/2/R393    most recent
00006.2005v1
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 Web of Science
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 Web of Science (5)
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Holloway, G. P.
Right arrow Articles by Tupling, A. R.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Holloway, G. P.
Right arrow Articles by Tupling, A. R.

ENVIRONMENTAL, EXERCISE AND RESPIRATORY PHYSIOLOGY

Differential effects of repetitive activity on sarcoplasmic reticulum responses in rat muscles of different oxidative potential

G. P. Holloway, H. J. Green, and A. R. Tupling

Department of Kinesiology, University of Waterloo, Waterloo, Ontario, Canada

Submitted 5 January 2005 ; accepted in final form 15 September 2005

We investigated the hypothesis that muscles of different oxidative potential would display differences in sarcoplasmic reticulum (SR) Ca2+ handling responses to repetitive contractile activity and recovery. Repetitive activity was induced in two muscles of high oxidative potential, namely, soleus (SOL) and red gastrocnemius (RG), and in white gastrocnemius (WG), a muscle of low oxidative potential, by stimulation in adult male rats. Measurements of SR properties, performed in crude homogenates, were made on control and stimulated muscles at the start of recovery (R0) and at 25 min of recovery (R25). Maximal Ca2+-ATPase activity (Vmax, µmol·g protein–1·min–1) at R0 was lower in stimulated SOL (105 ± 9 vs. 135 ± 7) and RG (269 ± 22 vs. 317 ± 26) and higher (P < 0.05) in WG (795 ± 32 vs. 708 ± 34). At R25, Vmax remained lower (P < 0.05) in SOL and RG but recovered in WG. Ca2+ uptake, measured at 2,000 nM, was depressed (P < 0.05) in SOL and RG by 34 and 13%, respectively, in stimulated muscles at R0 and remained depressed (P < 0.05) at R25. In contrast, Ca2+ uptake was elevated (P < 0.05) in stimulated WG at R0 by 9% and remained elevated (P < 0.05) at R25. Ca2+ release, unaltered in SOL and RG at both R0 and R25, was increased (P < 0.05) in stimulated WG at both R0 and R25. We conclude that SR Ca2+-handling responses to repetitive contractile activity and recovery are related to the oxidative potential of muscle.

skeletal muscles; contractile activity; calcium handling



Address for reprint requests and other correspondence: H. J. Green, Dept. of Kinesiology, Univ. of Waterloo, Waterloo, ON, Canada N2L 3G1 (e-mail: green{at}healthy.uwaterloo.ca)




This article has been cited by other articles:


Home page
J. Appl. Physiol.Home page
A. R. Tupling, C. Vigna, R. J. Ford, S. C. Tsuchiya, D. A. Graham, S. G. Denniss, and J. W. E. Rush
Effects of buthionine sulfoximine treatment on diaphragm contractility and SR Ca2+ pump function in rats
J Appl Physiol, December 1, 2007; 103(6): 1921 - 1928.
[Abstract] [Full Text] [PDF]


Home page
J. Appl. Physiol.Home page
T. A. Duhamel, H. J. Green, R. D. Stewart, K. P. Foley, I. C. Smith, and J. Ouyang
Muscle metabolic, SR Ca2+-cycling responses to prolonged cycling, with and without glucose supplementation
J Appl Physiol, December 1, 2007; 103(6): 1986 - 1998.
[Abstract] [Full Text] [PDF]




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