The Overlooked Role of Fiber Length in Mechanical Load-Induced Growth of Skeletal Muscle
Open accessAbstract
Dear Editor-in-Chief: Skeletal muscles that have been subjected to chronic mechanical overload typically present with a large increase in the total number of fibers per cross-section, and the review by Murach et al. (1) proposes that fiber splitting could, at least in part, explain this effect. To support their position, the first figure of their manuscript uses data from Roy and Edgerton (2) to argue that if an increase in muscle fiber cross-sectional area and pennation angle occur simultaneously, then there would be no net increase in the number of fibers per cross-section. However, their argument did not account for the 13% increase in muscle fiber length that was also reported by Roy and Edgerton (2). We believe that this was a critical oversight because, as illustrated below, subtle changes in fiber length could lead to a substantial increase in both the number of fibers per cross-section and the overall cross-sectional area of the muscle. Before explaining our position, we first want to state that we fully agree with Murach et al., in that models of chronic mechanical overload (e.g., synergist ablation) can induce a doubling in muscle mass within 1–2 wk, whereas substantial changes in the fiber cross-sectional area typically occur on a much slower time scale (1–2 months). Importantly, however, it has also been shown that chronic mechanical overload can lead to a very rapid increase in fiber length. For instance, Aoki et al. (3) reported that a ≈25% increase in both sarcomere number and fiber length can occur within 4 d after the onset of chronic stretch. Likewise, Williams and Goldspink (4) reported that 7 d of chronic mechanical overload (via tenotomy) led to a 25% increase in the number of sarcomeres per fiber. Based on these studies, it seems reasonable to propose that the 13% increase in fiber length reported by Roy and Edgerton could have occurred within a matter of days after the onset of mechanical overload. In Figure 1, we describe the key elements of a geometric model that can be used to predict the architectural properties of skeletal muscle (5). As shown in Figure 2, we used this model to assess what would happen if the plantaris muscle experienced a 13% increase in fiber length. The outcomes of our analysis revealed that, in the absence of any other changes (e.g., increase in fiber cross-sectional area, fiber splitting, etc.), a subtle 13% increase in fiber length would lead to a remarkable 52% increase in both the whole muscle cross-sectional area and the number of fibers per cross-section. Unfortunately, the majority of the studies in the field (including our own) have not measured fiber length. Yet, as recently summarized by Franchi et al. (6), there are strong indications that even resistance exercise in humans can lead to an increase in fiber length. Thus, it is our hope that this letter will help to raise awareness about the potentially profound role that changes in fiber length could play during various forms of mechanical load-induced growth.Figure 1: Geometric model of skeletal muscle architecture.Figure 2: Scale model of a plantaris muscle undergoing a 13% increase in fiber length.Kent W. JorgensonTroy A. Hornberger School of Veterinary Medicine and the Department of Comparative Biosciences University of Wisconsin–Madison Madison, WI
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
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?
Based on geometric modeling, relatively modest changes in FL can have disproportionately large effects on ACSA and muscle volume.
“based on geometric modeling it has recently been argued that relatively modest changes in FL can have disproportionately large effects on ACSA and muscle volume (46).”
From What makes long-term resistance-trained individuals so strong? A comparison of skeletal muscle morphology, architecture, and joint mechanics (2020) · cites this paper as [46]
Several other studies have found substantially greater muscle size of long-term resistance-trained participants (70% to 86%).
“Several other studies have found substantially greater muscle size of long-term resistance-trained participants [70% to 86% (9, 37, 46, 49)]”
From What makes long-term resistance-trained individuals so strong? A comparison of skeletal muscle morphology, architecture, and joint mechanics (2020) · cites this paper as [46]
Cites
The effect of immobilization on the longitudinal growth of striated muscle fibres.
WILLIAMS, P. E., & Goldspink, G. (1973) · PubMed · Cited by 331 · see citing works
Estimation of number of fibers in guinea pig skeletal muscles.
Maxwell, L., Faulkner, J. A., & Hyatt, G. J. (1974) · Journal of Applied Physiology · doi:10.1152/jappl.1974.37.2.259 · Cited by 80 · see citing works
Expression of genes related to myostatin signaling during rat skeletal muscle longitudinal growth
Aoki, M. S., Soares, A. G., Miyabara, E. H., Baptista, I. L., & Moriscot, A. S. (2009) · Muscle & Nerve · doi:10.1002/mus.21426 · Cited by 60 · see citing works
Muscle Fiber Splitting Is a Physiological Response to Extreme Loading in Animals
Murach, K. A., Dungan, C. M., Peterson, C. A., & McCarthy, J. J. (2019) · Exercise and Sport Sciences Reviews · doi:10.1249/jes.0000000000000181 · Cited by 48 · see citing works
Franchi, M. V., Atherton, P. J., Maganaris, C. N., & Narici, M. V. (2016) · SpringerPlus · doi:10.1186/s40064-015-1548-8 · Cited by 41 · see citing works
Response of mouse plantaris muscle to functional overload: comparison with rat and cat
Roy, R. R., & Edgerton, V. R. (1995) · Comparative Biochemistry and Physiology Part A Physiology · doi:10.1016/0300-9629(95)00062-c · Cited by 34 · see citing works
Flagged first, then by citations
Cited by
Sorted by citations
Roberts, M. D., McCarthy, J. J., Hornberger, T. A., Phillips, S. M., Mackey, A. L., Nader, G. A., Boppart, M. D., Kavazis, A. N., Reidy, P. T., Ogasawara, R., et al. (2023) · Physiological Reviews · doi:10.1152/physrev.00039.2022 · Cited by 214 · see citing works
Self-citationMaden-Wilkinson, T. M., Balshaw, T. G., Massey, G. J., & Folland, J. P. (2020) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00224.2019 · Cited by 81 · see citing works
Roberts, M. D., Haun, C. T., Vann, C. G., Osburn, S. C., & Young, K. C. (2020) · Frontiers in Physiology · doi:10.3389/fphys.2020.00816 · Cited by 66 · see citing works
Resistance exercise protects mice from protein-induced fat accretion
Trautman, M. E., Braucher, L. N., Elliehausen, C., Zhu, W. G., Zelenovskiy, E., Green, M., Sonsalla, M. M., Yeh, C.-Y., Hornberger, T. A., Konopka, A. R., et al. (2023) · eLife · doi:10.7554/elife.91007 · Cited by 8 · see citing works
Self-citationResistance exercise protects mice from protein-induced fat accretion
Trautman, M. E., Braucher, L. N., Elliehausen, C., Zhu, W. G., Zelenovskiy, E., Green, M., Sonsalla, M. M., Yeh, C.-Y., Hornberger, T. A., Konopka, A. R., et al. (2023) · doi:10.7554/elife.91007.2 · Cited by 1 · see citing works
Self-citation
- Authors
- Jorgenson, K. W., & Hornberger, T. A.
- Affiliations
- University of Wisconsin–Madison (US)
- Venue
- Exercise and Sport Sciences Reviews
- Published
- 2019-10
- Volume
- 47
- Issue
- 4
- Pages
- 258-259
- ISSN
- 0091-6331 (ISSN-L)
- 1538-3008
- PMC
- PMC6750012
- OpenAlex
- W2981422412
- Cited by
- 35
- References
- 6
- Citations by year
- 2026: 4 · 2025: 6 · 2024: 5 · 2023: 7 · 2022: 3 · 2021: 4 · 2020: 4 · 2019: 2
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Exercise and Sport Sciences Reviews (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Institute of General Medical Sciences (T32GM008688)
- National Institute of Arthritis and Musculoskeletal and Skin Diseases (R01AR057347)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Muscle Physiology and Disorders
- Health Sciences › Medicine › Complementary and alternative medicine › Cardiovascular and exercise physiology
- Physical Sciences › Engineering › Biomedical Engineering › Muscle activation and electromyography studies
- Keywords
- skeletal muscle hypertrophy, mechanical overload, muscle fiber length, fiber splitting, muscle architecture, sarcomere number, muscle cross-sectional area, synergist ablation, plantaris muscle, pennation angle, tenotomy, fiber cross-sectional area, muscle mass gain, muscle fiber cross-sectional area
- MeSH terms
- Animals, Muscle, Skeletal, Muscle Fibers, Skeletal
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review