Cited by 17Muscle Physiology and DisordersNutrition and Health in AgingNeurogenetic and Muscular Disorders Research

Voluntary wheel running with and without follistatin overexpression improves NMJ transmission but not motor unit loss in late life of C57BL/6J mice

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Chugh, Deepti, Iyer, Chitra C., Bobbili, Prameela, Blatnik, Anton J., Kaspar, Brian K., Meyer, Kathrin, Burghes, Arthur HM, Clark, Brian C. +1 more·2021·Neurobiology of Aging

Abstract

Sarcopenia, or pathological loss of muscle mass and strength during aging, is an important contributor to loss of physical function in older adults. Sarcopenia is a multifactorial syndrome associated with intrinsic muscle and upstream neurological dysfunction. Exercise is well-established as an effective intervention for sarcopenia, but less is known about the long-term neurobiological impact of exercise. The goals of this study were to investigate the effects of exercise, alone or in combination with follistatin (FST) overexpression (antagonist of myostatin), on neuromuscular junction transmission and motor unit numbers in mice between the age of 22 and 27 months, ages at which prior studies have demonstrated that some motor unit loss is already evident. C57BL/6J mice underwent baseline assessment and were randomized to housing with or without voluntary running wheels and injection with adeno-associated virus to overexpress FST or vehicle. Groups for comparison included sedentary and running with and without FST. Longitudinal assessments showed significantly increased muscle mass and contractility in the 'running plus FST' group, but running, with and without FST, showed no effect on motor unit degeneration. In contrast, running, with and without FST, demonstrated marked improvement of neuromuscular junction transmission stability.

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Crossref · 10.1016/j.neurobiolaging.2021.01.012

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  • Transgenic mice overexpressing follistatin that followed a voluntary wheel running program for 5 months showed a notable increase in muscle mass and contractility.

    “Transgenic mice overexpressing follistatin that followed a voluntary wheel running (speed >0.2 km/day) program for 5 months showed a notable increase in muscle mass and contractility [94] (Table 1).”

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References 72 · Cited by 17

Authors
Chugh, D., Iyer, C. C., Bobbili, P., Blatnik, A. J., Kaspar, B. K., Meyer, K., Burghes, A. H., Clark, B. C., & Arnold, W. D.
Affiliations
  • The Ohio State University Wexner Medical Center (US)
  • Nationwide Children's Hospital (US)
  • Ohio University (US)
Corresponding author
Arnold, W. David
Venue
Neurobiology of Aging
Publisher
Elsevier BV
Published
2021-05
Volume
101
Pages
285-296
ISSN
0197-4580 (ISSN-L)
OpenAlex
W3127040098
Cited by
17
References
72
Citations by year
2026: 1 · 2025: 7 · 2024: 3 · 2023: 1 · 2022: 2 · 2021: 3
FWCI
0.71
Type
journal article
Language
en
Open access
Locations
  • Neurobiology of Aging (publishedVersion)
  • PubMed (publishedVersion)
  • PubMed Central (acceptedVersion)
Funders
National Institute on Aging
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Muscle Physiology and Disorders
  • Health Sciences › Medicine › Physiology › Nutrition and Health in Aging
  • Health Sciences › Medicine › Genetics › Neurogenetic and Muscular Disorders Research
Keywords
voluntary wheel running, neuromuscular transmission, motor unit loss, sarcopenia, aging, physical activity, muscle mass, muscle contractility, AAV gene delivery, C57BL/6J mice
MeSH terms
Aging, Animals, Female, Male, Mice, Inbred C57BL, Motor Neurons, Synaptic Transmission, Neuromuscular Junction, Running, Gene Expression, Follistatin, Mice, Sarcopenia

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