Mechanotransduction and the regulation of protein synthesis in skeletal muscle
Open accessAbstract
Repeated bouts of resistance exercise produce an increase in skeletal muscle mass. The accumulation of protein associated with the growth process results from a net increase in protein synthesis relative to breakdown. While the effect of resistance exercise on muscle mass has long been recognized, the mechanisms underlying the link between high-resistance contractions and the regulation of protein synthesis and breakdown are, to date, poorly understood. In the present paper skeletal muscle will be viewed as a mechanosensitive cell type and the possible mechanisms through which mechanically-induced signalling events lead to changes in rates of protein synthesis will be examined.
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Murine synergistic ablation models cannot faithfully replicate the transcriptomic kinetics induced by voluntary resistance exercise in humans.
“While murine models utilizing synergistic ablation offer profound mechanistic insights, the extreme, non-physiological nature of such surgical overload cannot faithfully replicate the transcriptomic kinetics induced by voluntary resistance exercise in humans [83,84].”
From Ribosome Biogenesis as a Putative Bottleneck to Skeletal Muscle Hypertrophy: Mechanisms, Human Evidence, and Practical Modulators (2026) · cites this paper as [84]
The “Specificity in mechanotransduction” section says different mechanical loads can produce different adaptations, but it does not compare murine synergistic ablation with voluntary human resistance exercise. Searches for surgical overload and transcriptomic kinetics found no passage addressing whether the model can replicate the human time course; page numbers were unavailable in our copy. (LLM, conf=0.72)
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Cites
Mechanotransduction Across the Cell Surface and Through the Cytoskeleton
Wang, N., Butler, J. P., & Ingber, D. E. (1993) · Science · doi:10.1126/science.7684161 · Cited by 3,007 · see citing works
Integrins: Emerging Paradigms of Signal Transduction
Schwartz, M. A., Schaller, M. D., & Ginsberg, M. H. (1995) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev.cb.11.110195.003001 · Cited by 1,596 · see citing works
Molecular Basis of Mechanotransduction in Living Cells
Hamill, O. P., & Martinac, B. (2001) · Physiological Reviews · doi:10.1152/physrev.2001.81.2.685 · Cited by 1,124 · see citing works
Rapamycin suppresses 5′TOP mRNA translation through inhibition of p70s6k
Jefferies, H. B. J., Fumagalli, S., Dennis, P. B., Reinhard, C., Pearson, R. B., & Thomas, G. (1997) · The EMBO Journal · doi:10.1093/emboj/16.12.3693 · Cited by 934 · see citing works
Structure and function of phosphoinositide 3-kinases
Wymann, M. P., & Pirola, L. (1998) · Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids · doi:10.1016/s0005-2760(98)00139-8 · Cited by 662 · see citing works
<i>Physiology of a Microgravity Environment</i> Invited Review: Microgravity and skeletal muscle
Fitts, R. H., Riley, D. R., & Widrick, J. J. (2000) · Journal of Applied Physiology · doi:10.1152/jappl.2000.89.2.823 · Cited by 548 · see citing works
Mechanical stress-induced cardiac hypertrophy: mechanisms and signal transduction pathways
Ruwhof, C. (2000) · Cardiovascular Research · doi:10.1016/s0008-6363(00)00076-6 · Cited by 506 · see citing works
Plopper, G. E., McNamee, H., Dike, L. E., Bojanowski, K., & Ingber, D. E. (1995) · Molecular Biology of the Cell · doi:10.1091/mbc.6.10.1349 · Cited by 503 · see citing works
Rando, T. A. (2001) · Muscle & Nerve · doi:10.1002/mus.1192 · Cited by 425 · see citing works
Mechanism of work-induced hypertrophy of skeletal muscle
GOLDBERG, A. L., ETLINGER, J. D., GOLDSPINK, D. F., & JABLECKI, C. (1975) · Medicine and Science in Sports and Exercise · doi:10.1249/00005768-197500730-00016 · Cited by 402 · see citing works
The influence of immobilization and stretch on protein turnover of rat skeletal muscle.
Goldspink, D. F. (1977) · The Journal of Physiology · doi:10.1113/jphysiol.1977.sp011667 · Cited by 351 · see citing works
Modulation of GTPase activity of G proteins by fluid shear stress and phospholipid composition
Gudi, S., Nolan, J. P., & Frangos, J. A. (1998) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.95.5.2515 · Cited by 343 · see citing works
Kimball, S. R., Farrell, P. A., & Jefferson, L. S. (2002) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00221.2002 · Cited by 296 · see citing works
Exercise, Protein Metabolism, and Muscle Growth
Tipton, K. D., & Wolfe, R. R. (2001) · International Journal of Sport Nutrition and Exercise Metabolism · doi:10.1123/ijsnem.11.1.109 · Cited by 253 · see citing works
Dulhunty, A. F., & Franzini‐Armstrong, C. (1975) · The Journal of Physiology · doi:10.1113/jphysiol.1975.sp011068 · Cited by 241 · see citing works
Contraction Regulation of Akt in Rat Skeletal Muscle
Sakamoto, K., Hirshman, M. F., Aschenbach, W. G., & Goodyear, L. J. (2002) · Journal of Biological Chemistry · doi:10.1074/jbc.m112410200 · Cited by 192 · see citing works
Space travel directly induces skeletal muscle atrophy
Vandenburgh, H. H., Chromiak, J. A., Shansky, J., Tatto, M. D., & Lemaire, J. (1999) · The FASEB Journal · doi:10.1096/fasebj.13.9.1031 · Cited by 179 · see citing works
PROTEIN SYNTHESIS DURING WORK-INDUCED GROWTH OF SKELETAL MUSCLE
Goldberg, A. L. (1968) · The Journal of Cell Biology · doi:10.1083/jcb.36.3.653 · Cited by 152 · see citing works
Herbert, T. P., Kilhams, G. R., Batty, I. H., & Proud, C. G. (2000) · Journal of Biological Chemistry · doi:10.1074/jbc.275.15.11249 · Cited by 107 · see citing works
Vandenburgh, H. H., Shansky, J., Solerssi, R., & Chromiak, J. A. (1995) · Journal of Cellular Physiology · doi:10.1002/jcp.1041630209 · Cited by 103 · see citing works
Phosphorylation of 4E-BP1 Is Mediated by the p38/MSK1 Pathway in Response to UVB Irradiation
Liu, G., Zhang, Y., Bode, A. M., Ma, W., & Dong, Z. (2002) · Journal of Biological Chemistry · doi:10.1074/jbc.m110477200 · Cited by 82 · see citing works
Motion into mass: how does tension stimulate muscle growth?
Vandenburgh, H. H. (1987) · PubMed · Cited by 80 · see citing works
Palmer, R. M., Reeds, P. J., Atkinson, T., & Smith, R. H. (1983) · Biochemical Journal · doi:10.1042/bj2141011 · Cited by 70 · see citing works
Translation Control of Gene Expression
Oppenheim, A., Altuvia, S., Kornitzer, D., Teff, D., & Koby, S. (1991) · Journal of Basic and Clinical Physiology and Pharmacology · doi:10.1515/jbcpp.1991.2.3.223 · Cited by 41 · see citing works
The non-junctional sarcolemmal cytoskeleton: the costameres.
Anastasi, G., Cutroneo, G., Santoro, G., & Trimarchi, F. (1998) · PubMed · Cited by 17 · see citing works
Flagged first, then by citations
Cited by
Sorted by citations
A review on the mechanisms of blood-flow restriction resistance training-induced muscle hypertrophy
Pearson, S. J., & Hussain, S. R. (2015) · Sports Medicine · doi:10.1007/s40279-014-0264-9 · Cited by 592 · see citing works
Wernbom, M., Augustsson, J., & Thome??, R. (2007) · Sports Medicine · doi:10.2165/00007256-200737030-00004 · Cited by 583 · see citing works
Hornberger, T. A., Chu, W. K., Mak, Y. W., Hsiung, J. W., Huang, S. A., & Chien, S. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0600678103 · Cited by 312 · see citing works
Blood Flow Restricted Exercise and Skeletal Muscle Health
Manini, T. M., & Clark, B. C. (2009) · Exercise and Sport Sciences Reviews · doi:10.1097/jes.0b013e31819c2e5c · Cited by 296 · see citing works
The Structure and Role of Intramuscular Connective Tissue in Muscle Function
Purslow, P. P. (2020) · Frontiers in Physiology · doi:10.3389/fphys.2020.00495 · Cited by 229 · see citing works
O’Neil, T. K., Duffy, L. R., Frey, J. W., & Hornberger, T. A. (2009) · The Journal of Physiology · doi:10.1113/jphysiol.2009.173609 · Cited by 227 · see citing works
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
Mangine, G. T., Hoffman, J. R., Gonzalez, A. M., Townsend, J. R., Wells, A. J., Jajtner, A. R., Beyer, K. S., Boone, C. H., Miramonti, A. A., Wang, R., et al. (2015) · Physiological Reports · doi:10.14814/phy2.12472 · Cited by 204 · see citing works
Farup, J., de Paoli, F., Bjerg, K., Riis, S., Ringgard, S., & Vissing, K. (2015) · Scandinavian Journal of Medicine & Science in Sports · doi:10.1111/sms.12396 · Cited by 195 · see citing works
Cellular mechanisms regulating protein synthesis and skeletal muscle hypertrophy in animals
Miyazaki, M., & Esser, K. A. (2008) · Journal of Applied Physiology · doi:10.1152/japplphysiol.91355.2008 · Cited by 197 · see citing works
Ischemic strength training: a low‐load alternative to heavy resistance exercise?
Wernbom, M., Augustsson, J., & Raastad, T. (2008) · Scandinavian Journal of Medicine and Science in Sports · doi:10.1111/j.1600-0838.2008.00788.x · Cited by 169 · see citing works
Muscle structural assembly and functional consequences
Narici, M. V., Franchi, M. V., & Maganaris, C. N. (2016) · Journal of Experimental Biology · doi:10.1242/jeb.128017 · Cited by 157 · see citing works
Kramerova, I. A., Kudryashova, E., Venkatraman, G., & Spencer, M. J. (2005) · Human Molecular Genetics · doi:10.1093/hmg/ddi217 · Cited by 147 · see citing works
Neuroendocrine-immune interactions and responses to exercise
Fragala, M. S., Kraemer, W. J., Denegar, C. R., Maresh, C. M., Mastro, A. M., & Volek, J. S. (2011) · Sports Medicine · doi:10.2165/11590430-000000000-00000 · Cited by 145 · see citing works
Gundermann, D. M., Walker, D. K., Reidy, P. T., Borack, M. S., Dickinson, J. M., Volpi, E., & Rasmussen, B. B. (2014) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00600.2013 · Cited by 143 · see citing works
YAP-Mediated Mechanotransduction in Skeletal Muscle
Fischer, M., Rikeit, P., Knaus, P., & Coirault, C. (2016) · Frontiers in Physiology · doi:10.3389/fphys.2016.00041 · Cited by 145 · see citing works
Kalkhoven, J. T., Watsford, M. L., & Impellizzeri, F. M. (2020) · Journal of science and medicine in sport · doi:10.1016/j.jsams.2020.02.002 · Cited by 144 · see citing works
Atrophy and hypertrophy of skeletal muscles: structural and functional aspects
Boonyarom, O., & Inui, K. (2006) · Acta Physiologica · doi:10.1111/j.1748-1716.2006.01613.x · Cited by 137 · see citing works
Investigating the mechanisms of massage efficacy: the role of mechanical immunomodulation.
Waters-Banker, C., Dupont-Versteegden, E., Kitzman, P., & Butterfield, T. A. (2014) · Journal of athletic training · doi:10.4085/1062-6050-49.2.25 · Cited by 136 · see citing works
Wang, X. H., Du, J., Klein, J. D., Bailey, J. L., & Mitch, W. E. (2009) · Kidney International · doi:10.1038/ki.2009.260 · Cited by 129 · see citing works
Use of Flow, Electrical, and Mechanical Stimulation to Promote Engineering of Striated Muscles
Rangarajan, S., Madden, L. R., & Bursac, N. (2013) · Annals of Biomedical Engineering · doi:10.1007/s10439-013-0966-4 · Cited by 122 · see citing works
TACE release of TNF-α mediates mechanotransduction-induced activation of p38 MAPK and myogenesis
Zhan, M., Jin, B., Chen, S., Reecy, J. M., & Li, Y.-P. (2007) · Journal of Cell Science · doi:10.1242/jcs.03372 · Cited by 89 · see citing works
Franchi, M. V., Ruoss, S., Valdivieso, P., Mitchell, K. W., Smith, K., Atherton, P. J., Narici, M. V., & Flück, M. (2018) · Acta Physiologica · doi:10.1111/apha.13056 · Cited by 83 · see citing works
A map of the phosphoproteomic alterations that occur after a bout of maximal‐intensity contractions
Potts, G. K., McNally, R. M., Blanco, R., You, J., Hebert, A. S., Westphall, M. S., Coon, J. J., & Hornberger, T. A. (2017) · The Journal of Physiology · doi:10.1113/jp273904 · Cited by 83 · see citing works
The α7β1-integrin increases muscle hypertrophy following multiple bouts of eccentric exercise
Zou, K., Meador, B. M., Johnson, B., Huntsman, H. D., Mahmassani, Z. S., Valero, M. C., Huey, K. A., & Boppart, M. D. (2011) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00081.2011 · Cited by 79 · see citing works
Extracorporeal Shock Wave Therapy Accelerates Regeneration After Acute Skeletal Muscle Injury
Zissler, A., Steinbacher, P., Zimmermann, R. P., Pittner, S., Stoiber, W., Bathke, A. C., & Sänger, A. M. (2016) · The American Journal of Sports Medicine · doi:10.1177/0363546516668622 · Cited by 71 · see citing works
Exercise timing and circadian rhythms
Wolff, C. A., & Esser, K. A. (2019) · Current Opinion in Physiology · doi:10.1016/j.cophys.2019.04.020 · Cited by 69 · see citing works
Single vs. multi-joint resistance exercises: Effects on muscle strength and hypertrophy
Gentil, P., Soares, S., & Bottaro, M. (2015) · Asian Journal of Sports Medicine · doi:10.5812/asjsm.24057 · Cited by 67 · see citing works
A role for Raptor phosphorylation in the mechanical activation of mTOR signaling
Frey, J. W., Jacobs, B. L., Goodman, C. A., & Hornberger, T. A. (2013) · Cellular Signalling · doi:10.1016/j.cellsig.2013.11.009 · Cited by 60 · see citing works
Does blood flow restriction enhance hypertrophic signaling in skeletal muscle?
Meyer, R. A. (2006) · Journal of Applied Physiology · doi:10.1152/japplphysiol.01636.2005 · Cited by 54 · see citing works
Dunn, S. L., & Olmedo, M. L. (2016) · Physical Therapy · doi:10.2522/ptj.20150073 · Cited by 53 · see citing works
External physical and biochemical stimulation to enhance skeletal muscle bioengineering
Handschin, C., Mortezavi, A., Plock, J. A., & Eberli, D. (2014) · Advanced Drug Delivery Reviews · doi:10.1016/j.addr.2014.10.021 · Cited by 48 · see citing works
Thomas, A. C. Q., Stead, C. A., Burniston, J. G., & Phillips, S. M. (2024) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2024.08.010 · Cited by 52 · see citing works
Kosek, D. J., & Bamman, M. M. (2008) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00708.2007 · Cited by 44 · see citing works
Bae, K., Lee, K., Seo, Y.-U., Lee, H., Kim, D., & Choi, I. (2006) · Molecules and Cells · doi:10.1016/s1016-8478(23)17421-8 · Cited by 43 · see citing works
Frey, J. W., Farley, E. E., O’Neil, T. K., Burkholder, T. J., & Hornberger, T. A. (2009) · Biophysical Journal · doi:10.1016/j.bpj.2009.04.025 · Cited by 36 · see citing works
Innovations in Geroscience to enhance mobility in older adults
Anton, S. D., Cruz‐Almeida, Y., Singh, A., Alpert, J. M., Bensadon, B. A., Cabrera, M., Clark, D. J., Ebner, N. C., Esser, K. A., Fillingim, R. B., et al. (2020) · Experimental Gerontology · doi:10.1016/j.exger.2020.111123 · Cited by 37 · see citing works
Kim, H., Lee, S., & Choue, R. (2011) · Journal of the International Society of Sports Nutrition · doi:10.1186/1550-2783-8-10 · Cited by 33 · see citing works
Mahoney, D. J., & Tarnopolsky, M. A. (2005) · Physical Medicine and Rehabilitation Clinics of North America · doi:10.1016/j.pmr.2005.08.018 · Cited by 29 · see citing works
Zhang, N., Chim, Y. N., Wang, J., Wong, R. M. Y., Chow, S. K., & Cheung, W. (2019) · Journal of Orthopaedic Research® · doi:10.1002/jor.24477 · Cited by 29 · see citing works
Roberts, M. D., Holland, A. M., Kephart, W. C., Mobley, C. B., Mumford, P. W., Lowery, R. P., Fox, C. D., McCloskey, A. E., Shake, J. J., Mesquita, P. H. C., et al. (2015) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00837.2015 · Cited by 28 · see citing works
Disuse Atrophy of Human Skeletal Muscle
Urso, M. L. (2009) · Medicine & Science in Sports & Exercise · doi:10.1249/mss.0b013e3181a6458a · Cited by 28 · see citing works
Grosset, J., & Onambélé-Pearson, G. L. (2008) · The Anatomical Record · doi:10.1002/ar.20759 · Cited by 28 · see citing works
Deane, C. S., Phillips, B. E., Willis, C. R. G., Wilkinson, D. J., Smith, K., Higashitani, N., Williams, J. P., Szewczyk, N. J., Atherton, P. J., Higashitani, A., et al. (2022) · GeroScience · doi:10.1007/s11357-022-00658-5 · Cited by 27 · see citing works
Champ, C. E., Carpenter, D. J., Diaz, A. K., Rosenberg, J., Ackerson, B. G., & Hyde, P. N. (2022) · Sports Medicine · doi:10.1007/s40279-022-01759-z · Cited by 27 · see citing works
Mesenchymal Stem Cells Augment the Adaptive Response to Eccentric Exercise
Zou, K., Huntsman, H. D., VALERO, C. M., Adams, J. T., Skelton, J. T., Lisio, M. D., Jensen, T., & Boppart, M. D. (2014) · Medicine & Science in Sports & Exercise · doi:10.1249/mss.0000000000000405 · Cited by 27 · see citing works
Skiba, G. H., Andrade, S. F., & Rodacki, A. L. F. (2021) · Neurological Sciences · doi:10.1007/s10072-021-05307-x · Cited by 26 · see citing works
Nucleus Mechanosensing in Cardiomyocytes
Coscarella, I. L., Landim-Vieira, M., Rastegarpouyani, H., Chase, P. B., Irianto, J., & Pinto, J. R. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms241713341 · Cited by 25 · see citing works
Bird, S. P., Nienhuis, M. B., Biagioli, B., Pauw, K. D., & MEEUSEN, R. R. (2024) · Nutrients · doi:10.3390/nu16121886 · Cited by 26 · see citing works
Myonuclear alterations associated with exercise are independent of age in humans
Battey, E., Ross, J. A., Hoang, A., Wilson, D. G. S., Han, Y., Levy, Y., Pollock, R. D., Kalakoutis, M., Pugh, J. N., Close, G. L., et al. (2023) · The Journal of Physiology · doi:10.1113/jp284128 · Cited by 23 · see citing works
Favero, G. D., Woelflingseder, L., Janker, L., Neuditschko, B., Seriani, S., Gallina, P., Sbaizero, O., Gerner, C., & Marko, D. (2018) · Scientific Reports · doi:10.1038/s41598-018-29728-5 · Cited by 20 · see citing works
Cessation of contraction induces cardiomyocyte remodeling during zebrafish cardiogenesis
Yang, J., Hartjes, K. A., Nelson, T. J., & Xu, X. (2013) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.00721.2013 · Cited by 18 · see citing works
Campelj, D. G., Timpani, C. A., Petersen, A. C., Hayes, A., Goodman, C. A., & Rybalka, E. (2020) · Cancers · doi:10.3390/cancers12123810 · Cited by 17 · see citing works
Choi, I., Lee, K., Kim, M., Lee, M., & Park, K. (2005) · Journal of Cellular Biochemistry · doi:10.1002/jcb.20616 · Cited by 13 · see citing works
Evaluation of anabolic steroid induced renal damage with sonography in bodybuilders
Kantarcı, U. H., Pündük, Z., Şenarslan, Ö., & Dirik, A. (2018) · The Journal of Sports Medicine and Physical Fitness · doi:10.23736/s0022-4707.17.06763-9 · Cited by 12 · see citing works
Integrating Biophysics in Toxicology
Favero, G. D., & Kraegeloh, A. (2020) · Cells · doi:10.3390/cells9051282 · Cited by 12 · see citing works
CCN2 participates in overload-induced skeletal muscle hypertrophy
Petrosino, J. M., Longenecker, J. Z., Angell, C. D., Hinger, S. A., Martens, C. R., & Accornero, F. (2022) · Matrix Biology · doi:10.1016/j.matbio.2022.01.003 · Cited by 11 · see citing works
Genomic and Proteomic Approaches in Comparative Biochemistry and Physiology
Storey, K. B. (2006) · Physiological and Biochemical Zoology · doi:10.1086/499985 · Cited by 11 · see citing works
Regulation of mTOR signaling in skeletal muscle hypertrophy.
Esser, K. A. (2008) · PubMed · Cited by 10 · see citing works
Panisset, M. G., El‐Ansary, D., Dunlop, S. A., Marshall, R., Clark, J., Churilov, L. P., & Galea, M. P. (2020) · Journal of Spinal Cord Medicine · doi:10.1080/10790268.2020.1815480 · Cited by 10 · see citing works
Evaluation of in vitro macrophage differentiation during space flight
Ortega, M. T., Lu, N., & Chapes, S. K. (2012) · Advances in Space Research · doi:10.1016/j.asr.2012.02.021 · Cited by 9 · see citing works
Naimo, M. A., Rader, E. P., Ensey, J. S., Kashon, M. L., & Baker, B. A. (2019) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00582.2018 · Cited by 9 · see citing works
Benedini-Elias, P. C. O., Morgan, M. C., Cornachione, A. S., Martínez, E. Z., & Mattiello‐Sverzut, A. C. (2013) · Acta Histochemica · doi:10.1016/j.acthis.2013.10.008 · Cited by 7 · see citing works
Cação-Benedini, L. O., Ribeiro, P. G., Prado, C. M., Chesca, D. L., & Mattiello‐Sverzut, A. C. (2014) · Brazilian Journal of Medical and Biological Research · doi:10.1590/1414-431x20143521 · Cited by 5 · see citing works
Hesselink, M. K. C., & van Baak, M. A. (2004) · Proceedings of The Nutrition Society · doi:10.1079/pns2004353 · Cited by 4 · see citing works
Resistance exercise and mechanical overload upregulate vimentin for skeletal muscle remodeling
Godwin, J. S., Michel, J. M., Libardi, C. A., Kavazis, A. N., Fry, C. S., Frugé, A. D., McCashland, M., Vechetti, I. J., McCarthy, J. J., Mobley, C. B., et al. (2025) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.01028.2024 · Cited by 2 · see citing works
Morgalla, M. H., Marquetand, J. C., & Staber, F. K. (2023) · Pain Practice · doi:10.1111/papr.13324 · Cited by 2 · see citing works
Changes in BDNF Concentration in Men after Foam Roller Massage
Murawska‐Ciałowicz, E., Ciałowicz, M., Rosłanowski, A., Kaczmarek, A., Ratajczak‐Wielgomas, K., Kmiecik, A. M., Partyńska, A., Dzięgiel, P., & Andrzejewski, W. (2024) · Cells · doi:10.3390/cells13181564 · Cited by 2 · see citing works
Immunomodulatory Effec ts of Massage in Skeletal Muscle
Banker, C. W. (2013) · UKnowledge (University of Kentucky) · Cited by 2 · see citing works
Carson, J. A., & Puppa, M. (2012) · Springer eBooks · doi:10.1007/978-1-4614-4493-0_5 · Cited by 2 · see citing works
Hormone-mediated strategies to enhance training and performance
Beaven, C. M. (2010) · Tuwhera (Auckland University of Technology) · Cited by 2 · see citing works
Muñoz López, M., López-Gil, J. F., Ramírez de la piscina Viúdez, X., Baz-Valle, E., & Tornero Aguilera, J. F. (2026) · Cells · doi:10.3390/cells15111041 · Cited by 1 · see citing works
“While murine models utilizing synergistic ablation offer profound mechanistic insights, the extreme, non-physiological nature of such surgical overload cannot faithfully replicate the transcriptomic kinetics induced by voluntary resistance exercise in humans [83,84].”
Mechanisms and Efficacy of Massage Therapy for Post-Exercise Muscle Repair: A Narrative Review
Tiidus, P. M. (2026) · Muscles · doi:10.3390/muscles5020029 · Cited by 1 · see citing works
CALORIE RESTRICTION AS A MEANS TO CONTROL SKELETAL MUSCLE STIFFNESS IN AGED RATS
Pauwels, L. L., Dowling, B., Okafor, N., Breighner, R. E., & Domire, Z. J. (2012) · Journal of Musculoskeletal Research · doi:10.1142/s0218957712500194 · Cited by 1 · see citing works
Angleri, V., Damas, F., Stotzer, U. S., Selistre-de-Araújo, H. S., Santanielo, N., Soligon, S. D., Costa, L. A. R., Lixandrão, M. E., Conceição, M. S., VECHIN, F. C., et al. (2022) · Muscles · doi:10.3390/muscles1010002 · Cited by 1 · see citing works
El masaje, una técnica basada en la evidencia
Rulleau, T., Rivette, C., & Toussaint, L. (2017) · EMC - Kinesiterapia - Medicina Física · doi:10.1016/s1293-2965(17)85494-3 · Cited by 1 · see citing works
Leucine and exercise improve skeletal muscle function in the mdx mouse
Voelker, K. A. (2010) · VTechWorks (Virginia Tech)
The specificity of training adaptation in skeletal muscle
CAMERA, D. M. (2013) · RMIT Research Repository (RMIT University Library) · doi:10.25439/rmt.27576843
Skeletal Muscle Adaptations to Resistance Training with Ischemia
Elder, C. P., & McCully, K. K. (2008) · Medicine & Science in Sports & Exercise · doi:10.1249/01.mss.0000321477.90570.1a
Molecular Changes Following Skeletal Muscle Disuse in Humans
Reich, K. A. (2022) · ScholarWorks@UMassAmherst (University of Massachusetts Amherst) · doi:10.7275/1079181
Mechanical and metabolic stresses contribute to high force contraction signaling
Rahnert, J. A. (2012) · SMARTech Repository (Georgia Institute of Technology)
A Dissertation entitled The Impact of FoxO1 on Skeletal Muscle Protein Synthesis
Potter, R. A., & McLoughlin, T. J. (2014)
Phosphatidic Acid Increases Lean Body Tissue And Strength In Resistance Trained Men
Williams, D. R. (2012) · Journal of International Crisis and Risk Communication Research
Zou, K. (2014) · Illinois Digital Environment for Access to Learning and Scholarship (University of Illinois at Urbana-Champaign)
Il massaggio, approccio basato sulle evidenze
Rulleau, T., Rivette, C., & Toussaint, L. (2017) · EMC - Medicina Riabilitativa · doi:10.1016/s1283-078x(17)85845-4
Optimizing protein delivery to promote skeletal muscle protein synthesis
Areta, J. L. (2014) · RMIT Research Repository (RMIT University Library) · doi:10.25439/rmt.27351192
Phillips, S. M. (2020) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.727649711.793571158
Exercício físico como sincronizador do ritmo circadiano no câncer.
Teixeira, A. A. D. S. (2020) · doi:10.11606/t.42.2020.tde-05052021-134229
Hill, E. C., Proppe, C. E., Lubiak, S. M., Howard, M. A., Prajapati, A. J., Shah, N. M., Patel, N. N., Rivera, P. M., Zak, R., Schmidt, J. T., et al. (2025) · Journal of Neurophysiology · doi:10.1152/jn.00197.2025
The Repair Tax of Resistance Training: Microdamage Control as a Molecular Gatekeeper of Hypertrophy
Schaaf, K., Jacko, D., & Gehlert, S. (2026) · Exercise Science · doi:10.15857/ksep.2026.00059
Effects of prolonged physical training on skeletal muscle mass accrual throughout the life span
Ledergerber, R., Kotikangas, J., Cadore, E. L., Feuerbacher, J. F., & Schumann, M. (2026) · Best Practice & Research Clinical Endocrinology & Metabolism · doi:10.1016/j.beem.2026.102132
Baek, K., Ahn, Y. J., Kim, J.-S., & Lee, A. Y. (2026) · International Journal of Molecular Sciences · doi:10.3390/ijms27198609
Morgalla, M. (2026) · Frontiers in Pain Research · doi:10.3389/fpain.2026.1954865
- Authors
- Hornberger, T. A., & Esser, K. A.
- Affiliations
- University of Illinois Chicago (US)
- Venue
- Proceedings of The Nutrition Society
- Publisher
- Cambridge University Press (CUP)
- Published
- 2004-05
- Volume
- 63
- Issue
- 2
- Pages
- 331-335
- ISSN
- 0029-6651 (ISSN-L)
- 1475-2719
- OpenAlex
- W2063515332
- Cited by
- 102
- References
- 25
- Citations by year
- 2026: 6 · 2025: 2 · 2024: 3 · 2023: 4 · 2022: 5 · 2021: 1 · 2020: 8 · 2019: 5 · 2018: 3 · 2017: 4 · 2016: 4 · 2015: 4 · 2014: 10 · 2013: 7 · 2012: 7
- FWCI
- 1.51
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Proceedings of The Nutrition Society (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Aeronautics and Space Administration
- Pfizer
- National Institutes of Health
- National Institute of Arthritis and Musculoskeletal and Skin Diseases (AR 45617, R01AR045617)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Muscle metabolism and nutrition
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Muscle Physiology and Disorders
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Metabolism, Diabetes, and Cancer
- Keywords
- mechanotransduction, protein synthesis, skeletal muscle, resistance training, muscle hypertrophy, mechanosensitive cells, mechanical signalling, protein degradation, muscle mass
- MeSH terms
- Humans, Hypertrophy, Muscle Contraction, Muscle Proteins, Protein Biosynthesis, Weight Lifting, Exercise, Muscle, Skeletal
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