Evidence map›Paper›PMID 25762422›Full record

ArticleExperimental gerontology2015

Mouse forepaw lumbrical muscles are resistant to age-related declines in force production.

Katelyn A Russell, Rainer Ng, John A Faulkner, Dennis R Claflin, Christopher L Mendias

Abstract read
In one paragraph

Article in Experimental gerontology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.3field-weighted citation impact, top 38% of its field
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

4 citing papers in PubMed, 7 citations in OpenAlex.

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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

5 authors at 1 institution in 1 country.

Katelyn A RussellDepartment of Biomedical Engineering, University of Michigan, Ann Arbor, MI, United States.
Rainer NgDepartment of Biomedical Engineering, University of Michigan, Ann Arbor, MI, United States.
John A FaulknerDepartment of Biomedical Engineering, University of Michigan, Ann Arbor, MI, United States; Department of Molecular & Integrative Physiology, University of Michigan, Ann Arbor, MI, United States.
Dennis R ClaflinDepartment of Biomedical Engineering, University of Michigan, Ann Arbor, MI, United States; Department of Surgery, Section of Plastic Surgery, University of Michigan, Ann Arbor, MI, United States.
Christopher L MendiasDepartment of Molecular & Integrative Physiology, University of Michigan, Ann Arbor, MI, United States; Department of Orthopaedic Surgery, University of Michigan, Ann Arbor, MI, United States. Electronic address: cmendias@umich.edu.
University of Michigan · US

Funding

Research Education CoreP30AG024824 · NIA · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Neil Alexander · 2004 to 2026
$29.2M
Sex Differences in Tendon Growth and RemodelingR01AR063649 · NIAMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI RODEO, SCOTT A · 2013 to 2022
$3.6M
NIAMS NIH HHS R01 AR063649NIA NIH HHS P30 AG024824NIA NIH HHS P30-AG024824
6 · The paper itself

Abstract

A progressive loss of skeletal muscle mass and force generating capacity occurs with aging. Mice are commonly used in the study of aging-associated changes in muscle size and strength, with most models of aging demonstrating 15-35% reductions in muscle mass, cross-sectional area (CSA), maximum isometric force production (Po) and specific force (sPo), which is Po/CSA. The lumbrical muscle of the mouse forepaw is exceptionally small, with corresponding short diffusion distances that make it ideal for in vitro pharmacological studies and measurements of contractile properties. However, the aging-associated changes in lumbrical function have not previously been reported. To address this, we tested the hypothesis that compared to adult (12month old) mice, the forepaw lumbrical muscles of old (30month old) mice exhibit aging-related declines in size and force production similar to those observed in larger limb muscles. We found that the forepaw lumbricals were composed exclusively of fibers with type II myosin heavy chain isoforms, and that the muscles accumulated connective tissue with aging. There were no differences in the number of fibers per whole-muscle cross-section or in muscle fiber CSA. The whole muscle CSA in old mice was increased by 17%, but the total CSA of all muscle fibers in a whole-muscle cross-section was not different. No difference in Po was observed, and while sPo normalized to total muscle CSA was decreased in old mice by 22%, normalizing Po by the total muscle fiber CSA resulted in no difference in sPo. Combined, these results indicate that forepaw lumbrical muscles from 30month old mice are largely protected from the aging-associated declines in size and force production that are typically observed in larger limb muscles.

Indexed as

Age FactorsAgingAnimalsBody ConstitutionConnective TissueIsometric ContractionMiceModels, AnimalMuscle Fibers, SkeletalMyosin Heavy ChainsProtein IsoformsSkeletal Muscle MyosinsMyosin Heavy ChainsProtein IsoformsSkeletal Muscle MyosinsContractilityLumbrical muscleSarcopenia

Identifiers

PMID25762422
PMCPMC4397162
OpenAlexW1997583290

What OpenQuestion holds

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Read underepoch 390

Registered trials

None linked

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.