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PMID: 6214192 Published · ppublish English Journal Article Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S.

Effect of disuse on sarcoplasmic reticulum in fast and slow skeletal muscle.

The American journal of physiology ·Vol. 243 ·No. 3 ·1982-09-00 ·Pages C156-60

Kim DH, Witzmann FA, Fitts RH

Abstract

The effect of 6 wk of hindlimb immobilization on rat skeletal muscle sarcoplasmic reticulum (SR) was determined in the slow-twitch, type I soleus (SOL), the fast-twitch, type IIA deep region of the vastus lateralis (DVL), and the fast-twitch, type IIB superficial region of the vastus lateralis (SVL). Immobilization produced a significant decline in the Ca2+ uptake rate (Vmax) of SR vesicles from the slow SOL (0.930 +/- 0.116 to 0.365 +/- 0.071 mumol Ca2+ . mg-1 . min-1), while the SR Vmax increased in the fast SVL (2.763 +/- 0.133 to 5.209 +/- 0.687) and was unaltered in the DVL. Vesicles from the fast SVL and DVL also exhibited a higher total Ca2+ uptake capacity following immobilization. An evaluation of the time course of the immobilization-mediated effect revealed an increased Ca2+ uptake capacity in all three samples after 1 wk. In the SOL total Ca2+ uptake returned to control level after 2 wk, while in the fast-twitch muscles the higher capacities were maintained. The Ca2+-stimulated SR ATPase activity was not altered in any of the muscles studies, although the total SR ATPase activity increased twofold in the slow SOL.

MeSH Terms
Adenosine Triphosphatases/metabolism Animals Calcium/metabolism Female Immobilization Kinetics Muscles/physiopathology Rats Rats, Inbred Strains Sarcoplasmic Reticulum/physiology Time Factors
Chemicals
Adenosine Triphosphatases Calcium
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Kim D H
Witzmann F A
Fitts R H
Article Info
Journal
The American journal of physiology
Abbr.
Am J Physiol
ISSN
0002-9513
Published
1982-09-00
Pages
C156-60
Language
English
Region
United States
NLM ID
0370511
Subset
IM
Grants
NIADDK NIH HHS · AM-00810 · United States
NIADDK NIH HHS · AM-22037 · United States
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