Document Type
Article
Language
eng
Publication Date
4-2014
Publisher
American Physiological Society
Source Publication
American Journal of Physiology: Cell Physiology
Source ISSN
0002-9513
Abstract
Intense muscle contraction induces high rates of ATP hydrolysis with resulting increases in Pi, H+, and ADP, factors thought to induce fatigue by interfering with steps in the cross-bridge cycle. Force inhibition is less at physiological temperatures; thus the role of low pH in fatigue has been questioned. Effects of pH 6.2 and collective effects with 30 mM Pi on the pCa-force relationship were assessed in skinned fast and slow rat skeletal muscle fibers at 15 and 30°C. At 30°C, pH 6.2 + 30 mM Pi significantly depressed peak force in all fiber types, with the greatest effect in type IIx fibers. Across fiber types, Ca2+ sensitivity was depressed by low pH and low pH + high Pi, with the greater effect at 30°C. For type IIx fibers at 30°C, half-maximal activation (pCa50) was 5.36 at pH 6.2 (no added Pi) and 4.98 at pH 6.2 + 30 mM Pi compared with 6.58 in the control condition (pH 7, no added Pi). At 30°C, n2, reflective of thick filament cooperativity, was unchanged by low cell pH but was depressed from 5.02 to 2.46 in type IIx fibers with pH 6.2 + 30 mM Pi. With acidosis, activation thresholds of all fiber types required higher free Ca2+ at 15 and 30°C. With the exception of type IIx fibers, the Ca2+ required to reach activation threshold increased further with added Pi. In conclusion, it is clear that fatigue-inducing effects of low cell pH and elevated Pi at near-physiological temperatures are substantial.
Recommended Citation
Nelson, Cassandra R. and Fitts, Robert H., "Effects of Low Cell pH and Elevated Inorganic Phosphate on the pCa-Force Relationship in Single Muscle Fibers at Near-Physiological Temperatures" (2014). Biological Sciences Faculty Research and Publications. 590.
https://epublications.marquette.edu/bio_fac/590
Comments
Accepted version. American Journal of Physiology: Cell Physiology, Vol. 306, No. 7 (April 2014): C670-C678. DOI. © 2019 the American Physiological Society. Used with permission.