Evidence map›Paper›PMID 24486373›Full record

ArticleArchives of biochemistry and biophysics2014

Random myosin loss along thick-filaments increases myosin attachment time and the proportion of bound myosin heads to mitigate force decline in skeletal muscle.

Bertrand C W Tanner, Mark McNabb, Bradley M Palmer, Michael J Toth, Mark S Miller

Abstract read
In one paragraph

Article in Archives of biochemistry and biophysics, 2014. 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
1.0field-weighted citation impact, top 21% 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, 8 citations in OpenAlex.

  1. Article
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  4. Review
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 2 institutions in 1 country.

Bertrand C W TannerDepartment of Integrative Physiology and Neuroscience, Washington State University, Pullman, WA 99164, United States. Electronic address: btanner@vetmed.wsu.edu.
Mark McNabbDepartment of Integrative Physiology and Neuroscience, Washington State University, Pullman, WA 99164, United States.
Bradley M PalmerDepartment of Molecular Physiology and Biophysics, University of Vermont, Burlington, VT 05405, United States.
Michael J TothDepartment of Molecular Physiology and Biophysics, University of Vermont, Burlington, VT 05405, United States; Department of Medicine, University of Vermont, Burlington, VT 05405, United States.
Mark S MillerDepartment of Molecular Physiology and Biophysics, University of Vermont, Burlington, VT 05405, United States.
University of Vermont · USWashington State University · US

Funding

Ventricular and Cardiac Fiber Characterization and Integration CoreP01HL059408 · NHLBI · UNIVERSITY OF VERMONT &ST AGRIC COLLEGE · PI ROBBINS, JEFFREY · 1999 to 2014
$26.4M
POST-DOCTORAL CARDIOVASCULAR RESEARCH TRAINING PROGRAMT32HL007647 · NHLBI · UNIVERSITY OF VERMONT &ST AGRIC COLLEGE · PI LEWINTER, MARTIN M · 1988 to 2013
$3.3M
Muscle disuse and contractile dysfunction in the elderlyR01AG033547 · NIA · UNIVERSITY OF VERMONT & ST AGRIC COLLEGE · PI TOTH, MICHAEL J · 2010 to 2014
$1.9M
Skeletal muscle contractile dysfunction in heart failureR01HL077418 · NHLBI · UNIVERSITY OF VERMONT & ST AGRIC COLLEGE · PI TOTH, MICHAEL J · 2006 to 2009
$1.5M
Single Skeletal Muscle Fiber Mechanics and Myosin Kinetics in Human AgingK01AG031303 · NIA · UNIVERSITY OF VERMONT & ST AGRIC COLLEGE · PI MILLER, MARK STUART · 2008 to 2012
$611k
NHLBI NIH HHS P01 HL059408NHLBI NIH HHS P01-HL59408NHLBI NIH HHS R01 HL077418NHLBI NIH HHS R01-HL077418NHLBI NIH HHS T32 HL007647NHLBI NIH HHS T32-HL007647NIA NIH HHS K01 AG031303NIA NIH HHS K01-AG031303NIA NIH HHS R01 AG033547NIA NIH HHS R01-AG033547
6 · The paper itself

Abstract

Diminished skeletal muscle performance with aging, disuse, and disease may be partially attributed to the loss of myofilament proteins. Several laboratories have found a disproportionate loss of myosin protein content relative to other myofilament proteins, but due to methodological limitations, the structural manifestation of this protein loss is unknown. To investigate how variations in myosin content affect ensemble cross-bridge behavior and force production we simulated muscle contraction in the half-sarcomere as myosin was removed either (i) uniformly, from the Z-line end of thick-filaments, or (ii) randomly, along the length of thick-filaments. Uniform myosin removal decreased force production, showing a slightly steeper force-to-myosin content relationship than the 1:1 relationship that would be expected from the loss of cross-bridges. Random myosin removal also decreased force production, but this decrease was less than observed with uniform myosin loss, largely due to increased myosin attachment time (ton) and fractional cross-bridge binding with random myosin loss. These findings support our prior observations that prolonged ton may augment force production in single fibers with randomly reduced myosin content from chronic heart failure patients. These simulations also illustrate that the pattern of myosin loss along thick-filaments influences ensemble cross-bridge behavior and maintenance of force throughout the sarcomere.

Indexed as

Biomechanical PhenomenaComputer SimulationHumansKineticsModels, BiologicalModels, MolecularMuscle, SkeletalMyosinsSarcomeresMyosinsComputational modelingCross-bridge kineticsMuscle mechanicsSarcomere structureThick-filaments

Identifiers

PMID24486373
PMCPMC4043927
OpenAlexW2074580028

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.