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A dynamic calcium-force relationship model for sag behavior in fast skeletal muscle

Title
A dynamic calcium-force relationship model for sag behavior in fast skeletal muscle
Author(s)
Kim, HojeongHeckman, Charles
Issued Date
2023-06
Citation
PLoS Computational Biology, v.19, no.6, pp.e1011178
Type
Article
Keywords
SARCOMERE-LENGTHREGULATORY SITESCROSS-BRIDGESWHOLE MUSCLETROPONIN-CFAST-TWITCHMOTOR UNITSSLOW-TWITCHHISTOCHEMICAL PROFILESMEDIAL GASTROCNEMIUS
ISSN
1553-734X
Abstract
In vitro studies using isolated or skinned muscle fibers suggest that the sigmoidal relationship between the intracellular calcium concentration and force production may depend upon muscle type and activity. The goal of this study was to investigate whether and how the calcium-force relationship changes during force production under physiological conditions of muscle excitation and length in fast skeletal muscles. A computational framework was developed to identify the dynamic variation in the calcium-force relationship during force generation over a full physiological range of stimulation frequencies and muscle lengths in cat gastrocnemius muscles. In contrast to the situation in slow muscles such as the soleus, the calcium concentration for the half-maximal force needed to drift rightward to reproduce the progressive force decline, or sag behavior, observed during unfused isometric contractions at the intermediate length under low-frequency stimulation (i.e., 20 Hz). The slope at the calcium concentration for the half-maximal force was required to drift upward for force enhancement during unfused isometric contractions at the intermediate length under high-frequency stimulation (i.e., 40 Hz). The slope variation in the calcium-force relationship played a crucial role in shaping sag behavior across different muscle lengths. The muscle model with dynamic variations in the calcium-force relationship also accounted for the length-force and velocity-force properties measured under full excitation. These results imply that the calcium sensitivity and cooperativity of force-inducing crossbridge formation between actin and myosin filaments may be operationally altered in accordance with the mode of neural excitation and muscle movement in intact fast muscles. Copyright: © 2023 Kim, Heckman. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
URI
http://hdl.handle.net/20.500.11750/46343
DOI
10.1371/journal.pcbi.1011178
Publisher
Public Library of Science
Related Researcher
  • 김호정 Kim, Hojeong 바이오메디컬연구부
  • Research Interests Movement science; Neuromuscular physiology; Computational Medicine; Neural interface
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Division of Biotechnology 1. Journal Articles

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