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Related Experiment Video

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Isometric and Eccentric Force Generation Assessment of Skeletal Muscles Isolated from Murine Models of Muscular Dystrophies
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An acute eccentric exercise increases circulating myomesin 3 fragments.

Minjung Lee1, Jaehoon Shin1, Tatsuya Kato1

  • 1Faculty of Sport Sciences, Waseda University, 2-579-15 Mikajima, Tokorozawa, Saitama, 359-1192, Japan.

The Journal of Physiological Sciences : JPS
|January 20, 2021
PubMed
Summary

Researchers identified circulating myomesin 3 fragments as a novel biomarker for exercise-induced muscle damage. Levels increased 96 hours post-exercise, correlating with muscle symptoms and other damage markers.

Keywords:
BiomarkersEccentric exerciseMuscle damageMyomesin

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Area of Science:

  • Exercise Physiology
  • Biochemistry
  • Sports Medicine

Background:

  • Accurate assessment of exercise-induced muscle damage (EIMD) is crucial for athletes and coaches.
  • Current biomarkers for EIMD lack specificity or optimal detection timing.
  • Novel blood markers are needed to precisely evaluate muscle damage and recovery.

Purpose of the Study:

  • To investigate circulating myomesin 3 fragments as a potential novel biomarker for EIMD.
  • To assess the time course of myomesin 3 fragment changes following eccentric exercise.
  • To correlate myomesin 3 fragment levels with subjective muscle symptoms and established damage markers.

Main Methods:

  • Nine healthy males underwent a strenuous one-leg calf-raise exercise protocol (10 sets x 40 reps, 50% body weight load).
  • Blood samples were collected pre-exercise and at 2, 4, 24, 48, 72, and 96 hours post-exercise.
  • Muscle damage was assessed using a visual analog scale (VAS) for symptoms and plasma myomesin 3 fragment analysis.

Main Results:

  • Plasma myomesin 3 fragment levels showed a significant increase at 96 hours post-exercise.
  • Elevated myomesin 3 fragment levels positively correlated with visual analog scale (VAS) scores for muscle symptoms.
  • The changes in myomesin 3 fragments also correlated with other established biomarkers of muscle damage.

Conclusions:

  • Circulating myomesin 3 fragments show potential as a sensitive biomarker for detecting eccentric exercise-induced muscle damage.
  • Myomesin 3 fragments may provide valuable insights into the timing and extent of muscle damage and recovery.
  • Further research can validate myomesin 3 fragments for practical application in sports science and clinical settings.