Evidence map›Paper›PMID 24810676›Full record

ArticleMedical hypotheses2014

Muscle as a molecular machine for protecting joints and bones by absorbing mechanical impacts.

Armen Sarvazyan, Oleg Rudenko, Salavat Aglyamov, Stanislav Emelianov

Open access · greenAbstract read
In one paragraph

Article in Medical hypotheses, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.0field-weighted citation impact, top 25% 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

12 citing papers in PubMed, 27 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Neurophysiology of ACL Injury.Orthopedic reviews · 2025
    Article
  7. Article
  8. Article
  9. Article
  10. How muscle stiffness affects human body model behavior.Biomedical engineering online · 2021
    Article
  11. Article
  12. 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

4 authors at 3 institutions in 2 countries.

Armen SarvazyanARTANN Laboratories, Lambertville, NJ 08530, USA.
Oleg RudenkoDepartment of Physics, Moscow State University, Vorob'evy Gory, Moscow 119992, Russia.
Salavat AglyamovDepartment of Biomedical Engineering, University of Texas at Austin, Austin, TX 78712, USA. Electronic address: aglyamov@utexas.edu.
Stanislav EmelianovDepartment of Biomedical Engineering, University of Texas at Austin, Austin, TX 78712, USA.
The University of Texas at Austin · USArtann Laboratories, Inc. · USLomonosov Moscow State University · RU

Funding

Optical Coherence Elastography of the CorneaR01EY022362 · NEI · UNIVERSITY OF HOUSTON · PI Salavat R Aglyamov, Kirill V Larin · 2012 to 2026
$6.7M
Muscle viscosity as a protective mechanism for absorbing mechanical shockR21AR065024 · NIAMS · ARTANN LABORATORIES, INC. · PI SARVAZYAN, ARMEN · 2013 to 2014
$355k
NEI NIH HHS R01 EY022362NIAMS NIH HHS R21 AR065024NIAMS NIH HHS R21AR065024
6 · The paper itself

Abstract

We hypothesize that dissipation of mechanical energy of external impact to absorb mechanical shock is a fundamental function of skeletal muscle in addition to its primary function to convert chemical energy into mechanical energy. In physical systems, the common mechanism for absorbing mechanical shock is achieved with the use of both elastic and viscous elements and we hypothesize that the viscosity of the skeletal muscle is a variable parameter which can be voluntarily controlled by changing the tension of the contracting muscle. We further hypothesize that an ability of muscle to absorb shock has been an important factor in biological evolution, allowing the life to move from the ocean to land, from hydrodynamic to aerodynamic environment with dramatically different loading conditions for musculoskeletal system. The ability of muscle to redistribute the energy of mechanical shock in time and space and unload skeletal joints is of key importance in physical activities. We developed a mathematical model explaining the absorption of mechanical shock energy due to the increased viscosity of contracting skeletal muscles. The developed model, based on the classical theory of sliding filaments, demonstrates that the increased muscle viscosity is a result of the time delay (or phase shift) between the mechanical impact and the attachment/detachment of myosin heads to binding sites on the actin filaments. The increase in the contracted muscle's viscosity is time dependent. Since the forward and backward rate constants for binding the myosin heads to the actin filaments are on the order of 100s(-1), the viscosity of the contracted muscle starts to significantly increase with an impact time greater than 0.01s. The impact time is one of the key parameters in generating destructive stress in the colliding objects. In order to successfully dampen a short high power impact, muscles must first slow it down to engage the molecular mechanism of muscle viscosity. Muscle carries out two functions, acting first as a nonlinear spring to slow down impact and second as a viscous damper to absorb the impact. Exploring the ability of muscle to absorb mechanical shock may shed light to many problems of medical biomechanics and sports medicine. Currently there are no clinical devices for real-time quantitative assessment of viscoelastic properties of contracting muscles in vivo. Such assessment may be important for diagnosis and monitoring of treatment of various muscle disorders such as muscle dystrophy, motor neuron diseases, inflammatory and metabolic myopathies and many more.

Indexed as

Biomechanical PhenomenaBone and BonesElasticityHumansJointsMuscle, SkeletalViscosity

Identifiers

PMID24810676
PMCPMC4112738
OpenAlexW1992961783

What OpenQuestion holds

Textmetadata
LicenceTDM
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.