Evidence map›Paper›PMID 41801770›Full record

ArticleAmerican journal of physiology. Cell physiology2026

How temperature tunes muscle mechanics during eccentric contractions.

Graham N Askew, Roger W P Kissane

Abstract read
In one paragraph

Article in American journal of physiology. Cell physiology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors.

Graham N AskewSchool of Biomedical Sciences, University of Leeds, Leeds, United Kingdom.ORCID 0000-0003-1010-4439
Roger W P KissaneDepartment of Musculoskeletal and Ageing Science, University of Liverpool, Liverpool, United Kingdom.ORCID 0000-0001-9385-2584

Funding

UKRI | Biotechnology and Biological Sciences Research Council (AFRC) BB/R016917/1UKRI | Biotechnology and Biological Sciences Research Council (AFRC) BB/Y002466/1University of Liverpool (UoL) Early Career Researcher and Returners Fund
6 · The paper itself

Abstract

Eccentric muscle contractions occur when muscles actively lengthen, acting as brakes that dissipate energy and stabilize 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 nonphysiological temperatures. We studied active lengthening contractions in the 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.

Indexed as

Muscle ContractionMuscle, SkeletalActinsAnimalsBiomechanical PhenomenaConnectinMaleMiceMice, Inbred C57BLTemperatureActinsConnectineccentric contractionforce-velocityHill-type modelmuscle mechanicstitin

Identifiers

PMID41801770
PMCPMC7618963

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.