Evidence map›Paper›PMID 26289752›Full record

ArticleAmerican journal of physiology. Cell physiology2015

A new experimental model for force enhancement: steady-state and transient observations of the Drosophila jump muscle.

Ryan A Koppes, Douglas M Swank, David T Corr

Abstract read
In one paragraph

Article in American journal of physiology. Cell physiology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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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

2 citing papers in PubMed.

  1. Article
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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

3 authors.

Ryan A KoppesDepartment of Biomedical Engineering, Rensselaer Polytechnic Institute, Troy, New York; and.
Douglas M SwankDepartment of Biomedical Engineering, Rensselaer Polytechnic Institute, Troy, New York; and Department of Biological Sciences and Center for Biotechnology and Interdisciplinary Study, Rensselaer Polytechnic Institute, Troy, New York.
David T CorrDepartment of Biomedical Engineering, Rensselaer Polytechnic Institute, Troy, New York; and corrd@rpi.edu.

Funding

Modulating stretch activation to restore muscle and heart functionR01AR064274 · NIAMS · RENSSELAER POLYTECHNIC INSTITUTE · PI SWANK, DOUGLAS M · 2014 to 2018
$1.2M
NIAMS NIH HHS R01 AR064274
6 · The paper itself

Abstract

The increase in steady-state force after active lengthening in skeletal muscle, termed force enhancement (FE), has been observed for nearly one century. Although demonstrated experimentally at various structural levels, the underlying mechanism(s) remain unknown. We recently showed that the Drosophila jump muscle is an ideal model for investigating mechanisms behind muscle physiological properties, because its mechanical characteristics, tested thus far, duplicate those of fast mammalian skeletal muscles, and Drosophila has the advantage that it can be more easily genetically modified. To determine if Drosophila would be appropriate to investigate FE, we performed classic FE experiments on this muscle. Steady-state FE (FESS), following active lengthening, increased by 3, 7, and 12% of maximum isometric force, with increasing stretch amplitudes of 5, 10, and 20% of optimal fiber length (FLOPT), yet was similar for stretches across increasing stretch velocities of 4, 20, and 200% FLOPT/s. These FESS characteristics of the Drosophila jump muscle closely mimic those observed previously. Jump muscles also displayed typical transient FE characteristics. The transient force relaxation following active stretch was fit with a double exponential, yielding two phases of force relaxation: a fast initial relaxation of force, followed by a slower recovery toward steady state. Our analyses identified a negative correlation between the slow relaxation rate and FESS, indicating that there is likely an active component contributing to FE, in addition to a passive component. Herein, we have established the Drosophila jump muscle as a new and genetically powerful experimental model to investigate the underlying mechanism(s) of FE.

Indexed as

AnimalsDrosophilaIsometric ContractionMechanical PhenomenaModels, BiologicalMuscle, SkeletalMyosinsMyosinsDrosophilaforce enhancementhistory-dependent phenomenonskeletal muscletergal depressor of the trochanter

Identifiers

PMID26289752
PMCPMC4609653

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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.