Document Type
Article
Language
eng
Format of Original
9 p.
Publication Date
5-5-2004
Publisher
American Physiological Society
Source Publication
American Journal of Physiology - Cell Physiology
Source ISSN
0002-9513
Abstract
Elevated levels of Pi are thought to cause a substantial proportion of the loss in muscular force and power output during fatigue from intense contractile activity. However, support for this hypothesis is based, in part, on data from skinned single fibers obtained at low temperatures (≤15°C). The effect of high (30 mM) Pi concentration on the contractile function of chemically skinned single fibers was examined at both low (15°C) and high (30°C) temperatures using fibers isolated from rat soleus (type I fibers) and gastrocnemius (type II fibers) muscles. Elevating Pi from 0 to 30 mM at saturating free Ca2+ levels depressed maximum isometric force (Po) by 54% at 15°C and by 19% at 30°C (P < 0.05; significant interaction) in type I fibers. Similarly, the Po of type II fibers was significantly more sensitive to high levels of Pi at the lower (50% decrease) vs. higher temperature (5% decrease). The maximal shortening velocity of both type I and type II fibers was not significantly affected by elevated Pi at either temperature. However, peak fiber power was depressed by 49% at 15°C but by only 16% at 30°C in type I fibers. Similarly, in type II fibers, peak power was depressed by 40 and 18% at 15 and 30°C, respectively. These data suggest that near physiological temperatures and at saturating levels of intracellular Ca2+, elevated levels of Pi contribute less to fatigue than might be inferred from data obtained at lower temperatures.
Recommended Citation
Debold, Edward Patrick; Dave, H.; and Fitts, Robert, "Fiber Type and Temperature Dependence of Inorganic Phosphate: Implications for Fatigue" (2004). Biological Sciences Faculty Research and Publications. 50.
https://epublications.marquette.edu/bio_fac/50
Comments
Accepted version. American Journal of Physiology - Cell Physiology, Volume 287 (May 2004): C673-C681. DOI. © 2004 American Physiological Society. Used with permission.