Cited by 319Exercise and Physiological ResponsesMuscle Physiology and DisordersMuscle metabolism and nutrition

The DOI matches its Crossref record; 48 of the 48 references it cites were found in a registry or an index; none of the 29 sources its claims cite is checked for support yet.

Myofibre damage in human skeletal muscle: effects of electrical stimulation versus voluntary contraction

Open access
Crameri, R. M., Aagaard, P., Qvortrup, K., Langberg, H., Olesen, J., Kjær, M.·2007·The Journal of Physiology

Abstract

Disruption to proteins within the myofibre after a single bout of unaccustomed eccentric exercise is hypothesized to induce delayed onset of muscle soreness and to be associated with an activation of satellite cells. This has been shown in animal models using electrical stimulation but not in humans using voluntary exercise. Untrained males ( n = 8, range 22–27 years) performed 210 maximal eccentric contractions with each leg on an isokinetic dynamometer, voluntarily (VOL) with one leg and electrically induced (ES) with the other leg. Assessments from the skeletal muscle were obtained prior to exercise and at 5, 24, 96 and 192 h postexercise. Muscle tenderness rose in VOL and ES after 24 h, and did not differ between groups. Maximal isometric contraction strength, rate of force development and impulse declined in the VOL leg from 4 h after exercise, but not in ES (except at 24 h). In contrast, a significant disruption of cytoskeletal proteins (desmin) and a rise of myogenic growth factors (myogenin) occurred only in ES. Intracellular disruption and destroyed Z‐lines were markedly more pronounced in ES (40%) compared with VOL (10%). Likewise, the increase in satellite cell markers [neural cell adhesion molecule (N‐CAM) and paired‐box transcription factor (Pax‐7)] was more pronounced in ES versus VOL. Finally, staining of the intramuscular connective tissue (tenascin C) was increased equally in ES and VOL after exercise. The present study demonstrates that in human muscle, the delayed onset of muscle soreness was not significantly different between the two treatments despite marked differences in intramuscular histological markers, in particular myofibre proteins and satellite cell markers. An increase in tenascin C expression in the midbelly of the skeletal muscle in both legs provides further evidence of a potential role for the extracellular matrix in the phenomenon of delayed onset of muscle soreness.

Overview

Integrity signals

Registry

Crossref · 10.1113/jphysiol.2007.128827

Cites

48 of 48 references verified0 citation errors · 0 not checkable

Statistics

Nothing to recompute.

Verification

Claims the paper makes

0 of 29 cited sources checked · 0 supported · 0 flagged

Show all 73 claims

  • It may state two separate claims as one. 41
  • Probably not a substantial claim. 12
  • The quote only partly states this claim. 1
50 of 50
  • The paper relies on this without support.

    Baseline histological and molecular characteristics are equivalent between the two legs, even though the baseline biopsy was taken from only one leg.

    “Muscle samples were taken randomly from one leg 48 h prior to the exercise bout (baseline) and from both legs 5, 24, 96 and 192 h after the exercise bout.”
  • The paper relies on this without support.

    Electrical stimulation in this study represents the electrical stimulation used in previous animal studies.

    “electrical muscle stimulation (representing that of previous animal studies)”
  • The paper relies on this without support.

    The difference in myofibre damage between ES and VOL is due to differences in muscle activation pattern rather than the large difference in mechanical force or work between the two modes.

    “Quadriceps knee extension moment of force (peak moment, average moment in total range of motion), power (peak power, mean power) and contractile work during the 210 eccentric loading contractions were substantially greater for the voluntarily activated leg (VOL) than the electrostimulated leg (ES; P < 0.0001; Table 1).”
  • The paper relies on this without support.

    The extracellular matrix transfers up to 70% of the force produced by the myofibre.

    “Since the ECM is known to transfer up to 70% of muscle force produced by the myofibre”
  • The paper relies on this without support.

    The mass distribution, fibre pennation angle and fibre length are about the same for all quadriceps compartments.

    “Given that the mass distribution of 34%, the fibre pennation angle and the fibre length are about the same for all the quadriceps compartments”
5 of 5

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

Self-check

Percentages, sums and reported differences re-computed from the paper’s own numbers.

Each contradiction between two passages listed here was confirmed by an independent check.

  • Discussion incorrectly rules out VOL Z-line damage

    Major

    The discussion says significant Z-line damage was absent in VOL. The electron-microscopy results instead report significant disruption and an increase in fully destroyed Z-lines in that leg.

  • RFD100 suppression is assigned to the wrong follow-up time

    Minor

    The results say RFD100 was suppressed at 96 hours, but Table 2 marks the 192-hour VOL value as significant and does not mark the 96-hour value.

  • Relative-RFD changes cite a time point absent from the table

    Minor

    The results report a VOL relative-RFD reduction at 48 hours, but Table 2 has no 48-hour measurement; its follow-ups are 4, 24, 96 and 192 hours.

  • Discussion places the ES Pax-7 increase at 96 hours

    Minor

    The discussion reports increased ES Pax-7 at 96 hours. The results state that ES Pax-7 was significantly elevated at 192 hours only.

  • Figure 7 caption reverses the VOL desmin finding

    Minor

    The caption claims significant desmin-negative fibres in both legs, while the results explicitly state that none were found in VOL at any measured time. Figure 8's caption also says none were found in VOL.

  • Slow-trial mean-power percentage is incorrect

    Minor

    The ES mean power is 0.14/1.18 × 100 = 11.9% of the VOL value, not 5.9%.

    Reported 5.9 · recomputed 11.864407

  • IMP50 increase is assigned to the wrong follow-up time

    Minor

    The narrative places the ES increase at 96 hours, whereas Table 2 marks only the 192-hour ES value as significant.

  • Discussion calls ES MVC reductions significant despite the reported test

    Minor

    The discussion says both legs had significant MVC reductions at 4 and 24 hours. The results say ES MVC was unchanged apart from a 24-hour decrease, and Table 2 describes even that decrease as nonsignificant (P = 0.06).

  • Discussion overstates when VOL Pax-7 increased

    Minor

    The discussion reports increased VOL Pax-7 at both 96 and 192 hours, while the results say its significant increase occurred only at 96 hours.

  • ES relative-RFD significance is placed at 96 rather than 192 hours

    Minor

    The narrative identifies 96 hours as the exception to unchanged ES relative RFD. In Table 2, both ES relative-RFD rows carry significance marks at 192 hours, not 96 hours.

10 of 10

Citations

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Show all 48 references

Research works printed but not linked: 1

  1. Bergstrom J, 1962, Muscle electrolytes in man, Scan J Clin Lab Med, 14, 511

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Metadata

Authors
Crameri, R. M., Aagaard, P., Qvortrup, K., Langberg, H., Olesen, J., & Kjær, M.
Affiliations
  • Bispebjerg Hospital (DK)
  • University of Southern Denmark (DK)
  • University of Copenhagen (DK)
Corresponding author
Crameri, R. M.
Venue
The Journal of Physiology
Publisher
Wiley
Published
2007-08
Volume
583
Issue
1
Pages
365-380
ISSN
  • 0022-3751 (ISSN-L)
  • 1469-7793
OpenAlex
W1552699877
Cited by
319
References
48
Citations by year
2026: 9 · 2025: 12 · 2024: 14 · 2023: 13 · 2022: 10 · 2021: 20 · 2020: 15 · 2019: 20 · 2018: 17 · 2017: 15 · 2016: 22 · 2015: 13 · 2014: 23 · 2013: 12 · 2012: 24
FWCI
19.96
Type
journal article
Language
en
Open access
Locations
  • The Journal of Physiology (publishedVersion)
  • PubMed Central (publishedVersion)
  • PubMed (publishedVersion)
  • Research at the University of Copenhagen (University of Copenhagen) (publishedVersion)
  • Research at the University of Copenhagen (University of Copenhagen) (submittedVersion)
Topics
  • Health Sciences › Medicine › Physiology (medical) › Exercise and Physiological Responses
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Muscle Physiology and Disorders
  • Health Sciences › Nursing › Nutrition and Dietetics › Muscle metabolism and nutrition
Keywords
delayed onset muscle soreness, eccentric exercise, electrical stimulation, voluntary muscle contraction, satellite cells, desmin, myogenin, CD56, Pax7, tenascin-C, extracellular matrix, muscle contraction strength, rate of force development
MeSH terms
Adult, Biopsy, Electric Stimulation, Extracellular Matrix, Humans, Male, Muscle Contraction, Myofibrils, Pain, Vimentin, Biomarkers, Exercise, Muscle, Skeletal, Tenascin, Satellite Cells, Skeletal Muscle

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