Evidence map›Paper›PMID 39688124›Full record

ArticleThe Journal of experimental biology2025

Residual force enhancement is not altered while force depression is amplified at the cellular level in old age.

Binta S Njai, Avery Hinks, Makenna A Patterson, Geoffrey A Power

Abstract read
In one paragraph

Article in The Journal of experimental biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Binta S NjaiDepartment of Human Health and Nutritional Sciences, College of Biological Sciences, University of Guelph, Guelph, ON, Canada, N1G 2W1.
Avery HinksDepartment of Human Health and Nutritional Sciences, College of Biological Sciences, University of Guelph, Guelph, ON, Canada, N1G 2W1.
Makenna A PattersonDepartment of Human Health and Nutritional Sciences, College of Biological Sciences, University of Guelph, Guelph, ON, Canada, N1G 2W1.
Geoffrey A PowerDepartment of Human Health and Nutritional Sciences, College of Biological Sciences, University of Guelph, Guelph, ON, Canada, N1G 2W1.ORCID 0000-0003-2604-0740

Funding

Natural Sciences and Engineering Research Council of Canada RGPIN-2024-03782University of Guelph
6 · The paper itself

Abstract

Residual force enhancement (rFE) and residual force depression (rFD) are history-dependent properties of muscle which refer to increased and decreased isometric force following a lengthening or shortening contraction, respectively. The history dependence of force is greater in older than in younger human adults when assessed at the joint level. However, it is unclear whether this amplification of the history dependence of force in old age is owing to cellular mechanisms or is a consequence of age-related remodelling of muscle architecture. Single muscle fibres from the psoas major of old and young F344BN rats were dissected and chemically permeabilized. Single muscle fibres were mounted between a force transducer and length controller, then maximally activated (pCa 4.5). To assess rFD, fibres were actively shortened from 3.1 to 2.5 µm at both a slow (0.15 Lo s-1) and fast (0.6 Lo s-1) speed, with a fixed-end isometric reference contraction at 2.5 µm. To assess rFE, fibres were activated and stretched at 0.3 Lo s-1 from a sarcomere length of 2.2 to 2.5 µm, and 2.7 to 3.0 µm, and compared with fixed-end isometric reference contractions at 2.5 and 3.0 µm, respectively. Isometric force (2.5 µm) was ∼19% lower in muscle fibres from old as compared with young rats (P<0.001). Upon normalizing to fibre cross-sectional area, there was no age-related difference in specific force (P>0.05). rFD was ∼33% greater in muscle fibres from old as compared with young rats (P<0.05), while rFE did not differ between groups (P>0.05). rFD is amplified in old age at the cellular level, while rFE appears to be unchanged; thus, previously reported age-related modification of rFE occurs upstream from the cellular level.

Indexed as

AgingIsometric ContractionMuscle Fibers, SkeletalPsoas MusclesAnimalsBiomechanical PhenomenaMaleMuscle ContractionRatsRats, Inbred BNRats, Inbred F344Cross-bridgeHistory dependence of forceIsometric forceMuscle architectureSingle fibreStiffness

Identifiers

PMID39688124
PMCPMC11832184

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LicenceCC BY
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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.