How temperature tunes muscle mechanics during eccentric contractions

Eccentric muscle contractions occur when muscles actively lengthen, acting as brakes that dissipate energy and stabilise joints. When actively stretched, muscle force rises in two phases: an initial steep increase (phase 1), followed by a slower, sustained rise (phase 2). The temperature sensitivity of this response is poorly understood, despite its relevance for musculoskeletal models that often rely on data collected at non-physiological temperatures. We studied active lengthening contractions in mouse extensor digitorum longus muscle at 17°C, 27°C and 37°C. Force development in both phases was temperature sensitive. Phase 1 stiffness decreased at higher temperatures, consistent with faster ATP-dependent cross-bridge detachment, and contributions from mechanical strain-dependent detachment. In phase 2, stiffness increased with temperature, consistent with stronger and faster titin-actin interactions. The transition between phases (muscle 'give') varied with temperature and may reflect lower temperatures delaying cross-bridge detachment and engagement of the parallel elastic elements. Together, these findings highlight the intrinsic tuning of muscle mechanics, with potential implications for susceptibility to muscle damage under different thermal conditions, and provide a foundation for the development for more accurate musculoskeletal models.

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Publication Details

Journal
American Journal of Physiology-Cell Physiology
Published
2026-03-09
DOI
https://doi.org/10.1152/ajpcell.00047.2026
Primary Topic
Cardiomyopathy and Myosin Studies
Type
article
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article

How temperature tunes muscle mechanics during eccentric contractions

R. W. P. Kissane, Graham N. Askew
American Journal of Physiology-Cell Physiology
Cardiomyopathy and Myosin Studies
article

How temperature tunes muscle mechanics during eccentric contractions

R. W. P. Kissane, Graham N. Askew
article en

Abstract

Eccentric muscle contractions occur when muscles actively lengthen, acting as brakes that dissipate energy and stabilise joints. When actively stretched, muscle force rises in two phases: an initial steep increase (phase 1), followed by a slower, sustained rise (phase 2). The temperature sensitivity of this response is poorly understood, despite its relevance for musculoskeletal models that often rely on data collected at non-physiological temperatures. We studied active lengthening contractions in mouse extensor digitorum longus muscle at 17°C, 27°C and 37°C. Force development in both phases was temperature sensitive. Phase 1 stiffness decreased at higher temperatures, consistent with faster ATP-dependent cross-bridge detachment, and contributions from mechanical strain-dependent detachment. In phase 2, stiffness increased with temperature, consistent with stronger and faster titin-actin interactions. The transition between phases (muscle 'give') varied with temperature and may reflect lower temperatures delaying cross-bridge detachment and engagement of the parallel elastic elements. Together, these findings highlight the intrinsic tuning of muscle mechanics, with potential implications for susceptibility to muscle damage under different thermal conditions, and provide a foundation for the development for more accurate musculoskeletal models.

American Journal of Physiology-Cell Physiology
University of Leeds (GB), University of Liverpool (GB)
Affordable and clean energy
Openalex Percentile: Top 36%
Cardiomyopathy and Myosin Studies
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