Skeletal muscle regeneration and impact of aging and nutrition
Abstract
After skeletal muscle injury a regeneration process takes place to repair muscle. Skeletal muscle recovery is a highly coordinated process involving cross-talk between immune and muscle cells. It is well known that the physiological activities of both immune cells and muscle stem cells decline with advancing age, thereby blunting the capacity of skeletal muscle to regenerate. The age-related reduction in muscle repair efficiency contributes to the development of sarcopenia, one of the most important factors of disability in elderly people. Preserving muscle regeneration capacity may slow the development of this syndrome. In this context, nutrition has drawn much attention: studies have demonstrated that nutrients such as amino acids, n-3 polyunsaturated fatty acids, polyphenols and vitamin D can improve skeletal muscle regeneration by targeting key functions of immune cells, muscle cells or both. Here we review the process of skeletal muscle regeneration with a special focus on the cross-talk between immune and muscle cells. We address the effect of aging on immune and skeletal muscle cells involved in muscle regeneration. Finally, the mechanisms of nutrient action on muscle regeneration are described, showing that quality of nutrition may help to preserve the capacity for skeletal muscle regeneration with age.
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Chronic inflammation during ageing is associated with increased pro-inflammatory cytokines TNF-α and IL-6 compared to younger individuals due to possible dysregulation in immune cell function.
“On the other hand, chronic inflammation observed during ageing is associated with an increase in pro-inflammatory cytokines (compared to younger individuals) such as TNF-α and IL-6 due to possible dysregulation in immune cell function [59,76].”
From Potential Roles of n-3 PUFAs during Skeletal Muscle Growth and Regeneration (2018) · cites this paper as [76]
Cites
Holick, M. F. (2007) · New England Journal of Medicine · doi:10.1056/nejmra070553 · Cited by 13,720 · see citing works
The chemokine system in diverse forms of macrophage activation and polarization
MANTOVANI, A., SICA, A., SOZZANI, S., ALLAVENA, P., VECCHI, A., & LOCATI, M. (2004) · Trends in Immunology · doi:10.1016/j.it.2004.09.015 · Cited by 6,534 · see citing works
NF-κB AND REL PROTEINS: Evolutionarily Conserved Mediators of Immune Responses
Ghosh, S., May, M. J., & Kopp, E. B. (1998) · Annual Review of Immunology · doi:10.1146/annurev.immunol.16.1.225 · Cited by 5,182 · see citing works
Chronic Inflammation (Inflammaging) and Its Potential Contribution to Age-Associated Diseases
Franceschi, C., & Campisi, J. (2014) · The Journals of Gerontology Series A: Biological Sciences and Medical Sciences · doi:10.1093/gerona/glu057 · Cited by 3,891 · see citing works
Fadok, V. A., Bratton, D. L., Konowal, A., Freed, P. W., Westcott, J. Y., & Henson, P. M. (1998) · Journal of Clinical Investigation · doi:10.1172/jci1112 · Cited by 3,166 · see citing works
Muscles, exercise and obesity: skeletal muscle as a secretory organ
Pedersen, B. K., & Febbraio, M. A. (2012) · Nature Reviews Endocrinology · doi:10.1038/nrendo.2012.49 · Cited by 2,909 · see citing works
n−3 Polyunsaturated fatty acids, inflammation, and inflammatory diseases
Calder, P. C. (2006) · The American Journal of Clinical Nutrition · doi:10.1093/ajcn/83.6.1505s · Cited by 2,525 · see citing works
Muscle as an Endocrine Organ: Focus on Muscle-Derived Interleukin-6
Pedersen, B. K., & Febbraio, M. A. (2008) · Physiological Reviews · doi:10.1152/physrev.90100.2007 · Cited by 2,388 · see citing works
Rejuvenation of aged progenitor cells by exposure to a young systemic environment
Conboy, I. M., Conboy, M. J., Wagers, A. J., Girma, E. R., Weissman, I. L., & Rando, T. A. (2005) · Nature · doi:10.1038/nature03260 · Cited by 2,287 · see citing works
Satellite Cells and the Muscle Stem Cell Niche
Yin, H., Price, F., & Rudnicki, M. A. (2013) · Physiological Reviews · doi:10.1152/physrev.00043.2011 · Cited by 2,166 · see citing works
Arnold, L., Henry, A., Poron, F., Baba-Amer, Y., van Rooijen, N., Plonquet, A., Gherardi, R. K., & Chazaud, B. (2007) · The Journal of Experimental Medicine · doi:10.1084/jem.20070075 · Cited by 2,002 · see citing works
Myogenic satellite cells: physiology to molecular biology
Hawke, T. J., & Garry, D. J. (2001) · Journal of Applied Physiology · doi:10.1152/jappl.2001.91.2.534 · Cited by 1,646 · see citing works
Increased Wnt signaling during aging alters muscle stem cell fate and increases fibrosis
Brack, A. S., Conboy, M. J., Roy, S., Lee, M., Kuo, C. J., Keller, C., & Rando, T. A. (2007) · Science · doi:10.1126/science.1144090 · Cited by 1,564 · see citing works
NF-κB Controls Cell Growth and Differentiation through Transcriptional Regulation of Cyclin D1
D, D. C. G., Albanese, C., Reuther, J. Y., Pestell, R. G., & Baldwin, A. S. (1999) · Molecular and Cellular Biology · doi:10.1128/mcb.19.8.5785 · Cited by 1,304 · see citing works
A Special Population of Regulatory T Cells Potentiates Muscle Repair
Burzyn, D., Kuswanto, W., Kolodin, D., Shadrach, J. L., Cerletti, M., Jang, Y., Sefik, E., Tan, T. G., Wagers, A. J., Benoist, C., et al. (2013) · Cell · doi:10.1016/j.cell.2013.10.054 · Cited by 1,234 · see citing works
Notch-Mediated Restoration of Regenerative Potential to Aged Muscle
Conboy, I. M., Conboy, M. J., Smythe, G. M., & Rando, T. A. (2003) · Science · doi:10.1126/science.1087573 · Cited by 1,121 · see citing works
Regulatory interactions between muscle and the immune system during muscle regeneration
Tidball, J. G., & Villalta, S. A. (2010) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00735.2009 · Cited by 1,105 · see citing works
Age-dependent dysregulation of innate immunity
Shaw, A. C., Goldstein, D. R., & Montgomery, R. R. (2013) · Nature Reviews Immunology · doi:10.1038/nri3547 · Cited by 1,061 · see citing works
Conboy, I. M., & Rando, T. A. (2002) · Developmental Cell · doi:10.1016/s1534-5807(02)00254-x · Cited by 905 · see citing works
Interleukin-6 Is an Essential Regulator of Satellite Cell-Mediated Skeletal Muscle Hypertrophy
Serrano, A. L., Baeza-Raja, B., Perdiguero, E., Jardí, M., & Muñoz-Cánoves, P. (2008) · Cell Metabolism · doi:10.1016/j.cmet.2007.11.011 · Cited by 873 · see citing works
The aged niche disrupts muscle stem cell quiescence
Chakkalakal, J. V., Jones, K. M., Basson, M. A., & Brack, A. S. (2012) · Nature · doi:10.1038/nature11438 · Cited by 851 · see citing works
Sağ, D., Carling, D., Stout, R. D., & Suttles, J. (2008) · The Journal of Immunology · doi:10.4049/jimmunol.181.12.8633 · Cited by 798 · see citing works
Brack, A. S., Conboy, I. M., Conboy, M. J., Shen, J., & Rando, T. A. (2008) · Cell Stem Cell · doi:10.1016/j.stem.2007.10.006 · Cited by 682 · see citing works
Pedersen, B. K. (2011) · Journal of Experimental Biology · doi:10.1242/jeb.048074 · Cited by 668 · see citing works
Retrospective Birth Dating of Cells in Humans
Spalding, K. L., Bhardwaj, R. D., Buchholz, B. A., Druid, H., & Frisén, J. (2005) · Cell · doi:10.1016/j.cell.2005.04.028 · Cited by 626 · see citing works
Ruffell, D., Mourkioti, F., Gambardella, A., Kirstetter, P., Lopez, R. G., Rosenthal, N., & Nerlov, C. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0908641106 · Cited by 626 · see citing works
Paulsen, G., Mikkelsen, U. R., Raastad, T., & Peake, J. M. (2026) · PubMed · doi:10.22029/eir.2012.1668 · Cited by 572 · see citing works
Panda, A., Qian, F., Mohanty, S., van Duin, D., Newman, F. K., Zhang, L., Chen, S., Towle, V., Belshe, R. B., Fikrig, E., et al. (2010) · The Journal of Immunology · doi:10.4049/jimmunol.0901022 · Cited by 548 · see citing works
Hearps, A. C., Martin, G. E., Angelovich, T. A., Cheng, W., Maisa, A., Landay, A. L., Jaworowski, A., & Crowe, S. M. (2012) · Aging Cell · doi:10.1111/j.1474-9726.2012.00851.x · Cited by 547 · see citing works
p38 and Extracellular Signal-Regulated Kinases Regulate the Myogenic Program at Multiple Steps
Wu, Z.-G., Woodring, P. J., Bhakta, K. S., Tamura, K., Wen, F., Feramisco, J., Karin, M., Wang, J. Y. J., & Puri, P. (2000) · Molecular and Cellular Biology · doi:10.1128/mcb.20.11.3951-3964.2000 · Cited by 524 · see citing works
Villalta, S. A., Nguyen, H. X., Deng, B., Gotoh, T., & Tidball, J. G. (2008) · Human Molecular Genetics · doi:10.1093/hmg/ddn376 · Cited by 512 · see citing works
IL-4 Acts as a Myoblast Recruitment Factor during Mammalian Muscle Growth
Horsley, V., Jansen, K. M., Mills, S. T., & Pavlath, G. K. (2003) · Cell · doi:10.1016/s0092-8674(03)00319-2 · Cited by 508 · see citing works
Satellite-cell pool size does matter: Defining the myogenic potency of aging skeletal muscle
Shefer, G., de Mark, D. P. V., Richardson, J. B., & Yablonka‐Reuveni, Z. (2006) · Developmental Biology · doi:10.1016/j.ydbio.2006.02.022 · Cited by 506 · see citing works
Human innate immunosenescence: causes and consequences for immunity in old age
Panda, A., Arjona, A., Sapey, E., Bai, F., Fikrig, E., Montgomery, R. R., Lord, J. M., & Shaw, A. C. (2009) · Trends in Immunology · doi:10.1016/j.it.2009.05.004 · Cited by 502 · see citing works
Lenk, K., Schuler, G. C., & Adams, V. (2010) · Journal of Cachexia Sarcopenia and Muscle · doi:10.1007/s13539-010-0007-1 · Cited by 492 · see citing works
Philippidis, P., Mason, J. C., Evans, B. J., Nadra, I., Taylor, K. M., Haskard, D. O., & Landis, R. C. (2004) · Circulation Research · doi:10.1161/01.res.0000109414.78907.f9 · Cited by 476 · see citing works
IL-10 triggers changes in macrophage phenotype that promote muscle growth and regeneration
Deng, B., Wehling-Henricks, M., Villalta, S. A., Wang, Y., & Tidball, J. G. (2012) · The Journal of Immunology · doi:10.4049/jimmunol.1103180 · Cited by 472 · see citing works
Mounier, R., Théret, M., Arnold, L., Cuvellier, S., Bultot, L., Göransson, O., Sanz, N., Ferry, A., Sakamoto, K., Foretz, M., et al. (2013) · Cell Metabolism · doi:10.1016/j.cmet.2013.06.017 · Cited by 464 · see citing works
Sarcopenia, Cachexia and Aging: Diagnosis, Mechanisms and Therapeutic Options - A Mini-Review
Ali, S., & Garcia, J. M. (2014) · Gerontology · doi:10.1159/000356760 · Cited by 462 · see citing works
Effect of age on human neutrophil function
Wenisch, C., Patruta, S., Daxböck, F., Krause, R., & Hörl, W. H. (2000) · Journal of Leukocyte Biology · doi:10.1002/jlb.67.1.40 · Cited by 452 · see citing works
Chazaud, B., Sonnet, C., Lafuste, P., Bassez, G., Rimaniol, A., Poron, F., Authier, F., Dreyfus, P. A., & Gherardi, R. K. (2003) · The Journal of Cell Biology · doi:10.1083/jcb.200212046 · Cited by 452 · see citing works
The immune system and aging: A review
Castelo-Branco, C., & Soveral, I. (2014) · Gynecological Endocrinology · doi:10.3109/09513590.2013.852531 · Cited by 449 · see citing works
Agrawal, A., Agrawal, S., Cao, J.-N., Su, H., Osann, K., & Gupta, S. (2007) · The Journal of Immunology · doi:10.4049/jimmunol.178.11.6912 · Cited by 435 · see citing works
Inflammatory cytokines inhibit myogenic differentiation through activation of nuclear factor‐κΒ
LANGEN, R. C. J., Schols, A. M. W. J., KELDERS, M. C. J. M., Wouters, E. F. �., & Janssen-Heininger, Y. M. W. (2001) · The FASEB Journal · doi:10.1096/fj.00-0463 · Cited by 423 · see citing works
Saclier, M., Yacoub‐Youssef, H., Mackey, A. L., Arnold, L., Ardjoune, H., Magnan, M., Sailhan, F., Chelly, J., Pavlath, G. K., Mounier, R., et al. (2012) · Stem Cells · doi:10.1002/stem.1288 · Cited by 421 · see citing works
Muscle transplantation between young and old rats: age of host determines recovery
Carlson, B. M., & Faulkner, J. A. (1989) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.1989.256.6.c1262 · Cited by 417 · see citing works
Oxidized LDL and HDL: antagonists in atherothrombosis
Mertens, A. C., & Holvoet, P. (2001) · The FASEB Journal · doi:10.1096/fj.01-0273rev · Cited by 410 · see citing works
Chronic low-grade inflammation and age-related sarcopenia
Beyer, I., Mets, T., & Bautmans, I. (2012) · Current Opinion in Clinical Nutrition and Metabolic Care · doi:10.1097/mco.0b013e32834dd297 · Cited by 400 · see citing works
Satellite cells in human skeletal muscle; from birth to old age
Verdijk, L. B., Snijders, T., Drost, M., Delhaas, T., Kadi, F., & van Loon, L. J. C. (2014) · AGE · doi:10.1007/s11357-013-9583-2 · Cited by 399 · see citing works
Vitamin D and Its Role in Skeletal Muscle
Ceglia, L., & Harris, S. S. (2012) · Calcified Tissue International · doi:10.1007/s00223-012-9645-y · Cited by 388 · see citing works
Tidball, J. G., & Wehling‐Henricks, M. (2007) · The Journal of Physiology · doi:10.1113/jphysiol.2006.118265 · Cited by 375 · see citing works
Fadok, V. A., Bratton, D. L., Guthrie, L. A., & Henson, P. M. (2001) · The Journal of Immunology · doi:10.4049/jimmunol.166.11.6847 · Cited by 368 · see citing works
Age-Associated Defect in Human TLR-1/2 Function
van Duin, D., Mohanty, S., Thomas, V., Ginter, S., Montgomery, R. R., Fikrig, E., Allore, H. G., Medzhitov, R., & Shaw, A. C. (2007) · The Journal of Immunology · doi:10.4049/jimmunol.178.2.970 · Cited by 352 · see citing works
Gómez, C. R., Nomellini, V., Faunce, D. E., & Kovacs, E. J. (2008) · Experimental Gerontology · doi:10.1016/j.exger.2008.05.016 · Cited by 328 · see citing works
A Population of Myogenic Stem Cells That Survives Skeletal Muscle Aging
Collins, C. A., Zammit, P. S., Ruiz, A. P., Morgan, J. E., & Partridge, T. A. (2007) · Stem Cells · doi:10.1634/stemcells.2006-0372 · Cited by 320 · see citing works
Tumor necrosis factor-alpha inhibits myogenic differentiation through myod protein destabilization
Langen, R. C. J., van der Velden, J. L. J., Schols, A. M. W. J., Kelders, M. C. J. M., Wouters, E. F. M., & Janssen‐Heininger, Y. M. W. (2004) · The FASEB Journal · doi:10.1096/fj.03-0251com · Cited by 319 · see citing works
Ramprasad, M. P., Fischer, W., Witztum, J. L., Sambrano, G. R., Quehenberger, O., & Steinberg, D. H. (1995) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.92.21.9580 · Cited by 311 · see citing works
Decary, S., Mouly, V., Hamida, C. B., Sautet, A., Barbet, P., & Butler-Browne, G. S. (1997) · Human Gene Therapy · doi:10.1089/hum.1997.8.12-1429 · Cited by 304 · see citing works
Macrophage Plasticity and the Role of Inflammation in Skeletal Muscle Repair
Kharraz, Y., Guerra, J., Mann, C. J., Serrano, A. L., & Muñoz‐Cánoves, P. (2013) · Mediators of Inflammation · doi:10.1155/2013/491497 · Cited by 302 · see citing works
TNF-α regulates myogenesis and muscle regeneration by activating p38 MAPK
Chen, S., Jin, B., & Li, Y.-P. (2006) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00486.2006 · Cited by 301 · see citing works
Villalta, S. A., Rinaldi, C., Deng, B., Liu, G., Fedor, B., & Tidball, J. G. (2011) · Human Molecular Genetics · doi:10.1093/hmg/ddq523 · Cited by 299 · see citing works
Pillon, N. J., Bilan, P. J., Fink, L. N., & Klip, A. (2013) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00553.2012 · Cited by 285 · see citing works
The Role of Macrophages in Skeletal Muscle Regeneration with Particular Reference to Chemotaxis
Robertson, T. A., Maley, M. A. L., Grounds, M. D., & Papadimitriou, J. M. (1993) · Experimental Cell Research · doi:10.1006/excr.1993.1199 · Cited by 283 · see citing works
Zhang, C., Li, Y., Wu, Y., Wang, L., Wang, X., & Du, J. (2013) · Journal of Biological Chemistry · doi:10.1074/jbc.m112.419788 · Cited by 279 · see citing works
Hakim, F. T., Flomerfelt, F. A., Boyiadzis, M. M., & Gress, R. E. (2004) · Current Opinion in Immunology · doi:10.1016/j.coi.2004.01.009 · Cited by 272 · see citing works
The involvement of the ubiquitin proteasome system in human skeletal muscle remodelling and atrophy
Murton, A. J., Constantin, D., & Greenhaff, P. L. (2008) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2008.10.011 · Cited by 265 · see citing works
Lu, H., Huang, D., Saederup, N., Charo, I. F., Ransohoff, R. M., & Zhou, L. (2010) · The FASEB Journal · doi:10.1096/fj.10-171579 · Cited by 260 · see citing works
Lu, H., Huang, D., Ransohoff, R. M., & Zhou, L. (2011) · The FASEB Journal · doi:10.1096/fj.10-178939 · Cited by 255 · see citing works
Day, K., Shefer, G., Shearer, A., & Yablonka-Reuveni, Z. (2010) · Developmental Biology · doi:10.1016/j.ydbio.2010.01.006 · Cited by 254 · see citing works
Regulatory T cells suppress muscle inflammation and injury in muscular dystrophy
Villalta, S. A., Rosenthal, W. L., Martinez, L., Kaur, A., Sparwasser, T. D., Tidball, J. G., Margeta, M., Spencer, M. J., & Bluestone, J. A. (2014) · Science Translational Medicine · doi:10.1126/scitranslmed.3009925 · Cited by 253 · see citing works
TNF-α is a mitogen in skeletal muscle
Li, Y.-P. (2003) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00453.2002 · Cited by 249 · see citing works
Impaired functions of peripheral blood monocyte subpopulations in aged humans
Nyugen, J., Agrawal, S., Gollapudi, S., & Gupta, S. (2010) · Journal of Clinical Immunology · doi:10.1007/s10875-010-9448-8 · Cited by 249 · see citing works
Monocyte/macrophage interactions with myogenic precursor cells during skeletal muscle regeneration
Saclier, M., Cuvellier, S., Magnan, M., Mounier, R., & Chazaud, B. (2013) · FEBS Journal · doi:10.1111/febs.12166 · Cited by 248 · see citing works
Baeza-Raja, B., & Muñoz-Cánoves, P. (2004) · Molecular Biology of the Cell · doi:10.1091/mbc.e03-08-0585 · Cited by 247 · see citing works
What does chronic electrical stimulation teach us about muscle plasticity?
Pette, D., & Vrbov�, G. (1999) · Muscle & Nerve · doi:10.1002/(sici)1097-4598(199906)22:6 · Cited by 246 · see citing works
Molecular aging and rejuvenation of human muscle stem cells
Carlson, M. E., Suetta, C., Conboy, M. J., Aagaard, P., Mackey, A., Kjaer, M., & Conboy, I. (2009) · EMBO Molecular Medicine · doi:10.1002/emmm.200900045 · Cited by 245 · see citing works
The effects of obesity on skeletal muscle regeneration
Akhmedov, D., & Berdeaux, R. (2013) · Frontiers in Physiology · doi:10.3389/fphys.2013.00371 · Cited by 241 · see citing works
Vitamin D and Innate and Adaptive Immunity
Hewison, M. (2011) · Vitamins and hormones · doi:10.1016/b978-0-12-386960-9.00002-2 · Cited by 239 · see citing works
Dual and Beneficial Roles of Macrophages During Skeletal Muscle Regeneration
Chazaud, B., Brigitte, M., Yacoub-Youssef, H., Arnold, L., Gherardi, R., Sonnet, C., Lafuste, P., & Chrétien, F. (2009) · Exercise and sport sciences reviews · doi:10.1097/jes.0b013e318190ebdb · Cited by 238 · see citing works
IL-7 is expressed and secreted by human skeletal muscle cells
Haugen, F., Norheim, F., Lian, H., Wensaas, A. J., Dueland, S., Berg, O., Funderud, A., Skålhegg, B. S., Raastad, T., & Drevon, C. A. (2010) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00094.2009 · Cited by 237 · see citing works
Perdiguero, E., Sousa-Victor, P., Ruiz-Bonilla, V., Jardí, M., Caelles, C., Serrano, A. L., & Muñoz-Cánoves, P. (2011) · Journal of Cell Biology · doi:10.1083/jcb.201104053 · Cited by 236 · see citing works
Physiopathological Mechanism of Sarcopenia
Walrand, S., Guillet, C., Salles, J., Cano, N., & Boirie, Y. (2011) · Clinics in Geriatric Medicine · doi:10.1016/j.cger.2011.03.005 · Cited by 235 · see citing works
Pizza, F. X., Peterson, J. M., Baas, J. H., & Koh, T. J. (2004) · The Journal of Physiology · doi:10.1113/jphysiol.2004.073965 · Cited by 228 · see citing works
Teixeira, C. F., Zamuner, S., Zuliani, J., Fernandes, C. M., Cruz-Hofling, M. A., Fernandes, I., Chaves, F., & Gutiérrez, J. (2003) · Muscle and Nerve · doi:10.1002/mus.10453 · Cited by 223 · see citing works
Age-related changes in natural killer cell receptors from childhood through old age
Almeida-Oliveira, A., Smith-Carvalho, M., Pôrto, L. C., Cardoso-Oliveira, J., Ribeiro, A. D. S., Falcão, R. R., Abdelhay, E., Bouzas, L. F., Thuler, L. C. S., Ornellas, M. H., et al. (2011) · Human Immunology · doi:10.1016/j.humimm.2011.01.009 · Cited by 223 · see citing works
Inflamm-aging: autoimmunity, and the immune-risk phenotype
Boren, E. J., & Gershwin, M. E. (2004) · Autoimmunity Reviews · doi:10.1016/j.autrev.2004.03.004 · Cited by 222 · see citing works
Lolmede, K., Campana, L., Vezzoli, M., Bosurgi, L., Tonlorenzi, R., Clementi, E., Bianchi, M. E., Cossu, G., Manfredi, A. A., Brunelli, S., et al. (2009) · Journal of Leukocyte Biology · doi:10.1189/jlb.0908579 · Cited by 216 · see citing works
Innate and adaptive immunosenescence
Agarwal, S., & Busse, P. J. (2010) · Annals of Allergy Asthma & Immunology · doi:10.1016/j.anai.2009.11.009 · Cited by 215 · see citing works
Endogenous interferon-γ is required for efficient skeletal muscle regeneration
Cheng, M., Nguyen, M.-H., Fantuzzi, G., & Koh, T. J. (2008) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00568.2007 · Cited by 214 · see citing works
Niwa, Y., Kasama, T., Miyachi, Y., & KANOH, T. (1989) · Life Sciences · doi:10.1016/0024-3205(89)90482-7 · Cited by 204 · see citing works
Macrophage Plasticity in Skeletal Muscle Repair
Rigamonti, E., Zordan, P., Sciorati, C., Rovere-Querini, P., & Brunelli, S. (2014) · BioMed Research International · doi:10.1155/2014/560629 · Cited by 196 · see citing works
Brigitte, M., Schilte, C., Plonquet, A., Baba‐Amer, Y., Henry, A., Charlier, C., Tajbakhsh, S., Albert, M. L., Gherardi, R. K., & Chrétien, F. C. (2009) · Arthritis & Rheumatism · doi:10.1002/art.27183 · Cited by 192 · see citing works
Aging is associated with increased regulatory T ‐cell function
Garg, S. K., Delaney, C. E., Toubai, T., Ghosh, A. K., Reddy, P. R., Banerjee, R. V., & Yung, R. L. (2013) · Aging Cell · doi:10.1111/acel.12191 · Cited by 184 · see citing works
Nguyen, H. X., & Tidball, J. (2003) · Journal of Physiology · doi:10.1111/j..2002.00125.x · Cited by 181 · see citing works
Skeletal muscle regeneration and the mitotic clock
Renault, V. M., Piron-Hamelin, G., Forestier, C.-L., Donna, S. D., Decary, S., Hentati, F., Saillant, G., Butler-Browne, G. S., & Mouly, V. (2000) · Experimental Gerontology · doi:10.1016/s0531-5565(00)00151-0 · Cited by 179 · see citing works
Age-Related Changes in Eosinophil Function in Human Subjects
Mathur, S. K., Schwantes, E. A., Jarjour, N. N., & Busse, W. W. (2008) · CHEST Journal · doi:10.1378/chest.07-2114 · Cited by 179 · see citing works
Ochoa, O., Sun, D., Reyna, S. M., Waite, L. L., Michalek, J. E., McManus, L. M., & Shireman, P. K. (2007) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00069.2007 · Cited by 178 · see citing works
Srikuea, R., Zhang, X., Park-Sarge, O.-K., & Esser, K. A. (2012) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00014.2012 · Cited by 177 · see citing works
Myonuclear apoptosis in dystrophic mdx muscle occurs by perforin-mediated cytotoxicity.
Spencer, M. J., Walsh, C. M., Dorshkind, K. A., Rodriguez, E. M., & Tidball, J. G. (1997) · Journal of Clinical Investigation · doi:10.1172/jci119464 · Cited by 176 · see citing works
Sonnet, C., Lafuste, P., Arnold, L., Brigitte, M., Poron, F., Authier, F., Chrétien, F. C., Gherardi, R. K., & Chazaud, B. (2006) · Journal of Cell Science · doi:10.1242/jcs.02988 · Cited by 169 · see citing works
Chemokine receptor CCR2 involvement in skeletal muscle regeneration
Warren, G. L., Hulderman, T., Mishra, D., Gao, X., Millecchia, L., O’Farrell, L., Kuziel, W. A., & Simeonova, P. P. (2004) · The FASEB Journal · doi:10.1096/fj.04-2421fje · Cited by 167 · see citing works
The Role of Tumor Necrosis Factor-alpha (TNF-α) in Skeletal Muscle Regeneration
Collins, R. A., & Grounds, M. D. (2001) · Journal of Histochemistry & Cytochemistry · doi:10.1177/002215540104900807 · Cited by 161 · see citing works
Przybyla, B., Gurley, C., Harvey, J. F., Bearden, E., Kortebein, P., Evans, W., Sullivan, D., Peterson, C. A., & Dennis, R. (2006) · Experimental Gerontology · doi:10.1016/j.exger.2005.12.007 · Cited by 158 · see citing works
Villalta, S. A., Deng, B., Rinaldi, C., Wehling-Henricks, M., & Tidball, J. G. (2011) · The Journal of Immunology · doi:10.4049/jimmunol.1101267 · Cited by 158 · see citing works
Owens, D. J., Sharples, A. P., Polydorou, I., Alwan, N., Donovan, T. F., TANG, J. C. Y., Fraser, W. D., Cooper, R. G., Morton, J. P., Stewart, C. E., et al. (2015) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00375.2015 · Cited by 156 · see citing works
LIF is a contraction-induced myokine stimulating human myocyte proliferation
Broholm, C., Laye, M. J., Brandt, C., Vadalasetty, R., Pilegaard, H., Pedersen, B. K., & Scheele, C. C. (2011) · Journal of Applied Physiology · doi:10.1152/japplphysiol.01399.2010 · Cited by 155 · see citing works
Age‐associated elevation in TLR5 leads to increased inflammatory responses in the elderly
Qian, F., Wang, X., Zhang, L., Chen, S., Piecychna, M., Allore, H., Bockenstedt, L., Malawista, S., Bucala, R., Shaw, A. C., et al. (2012) · Aging Cell · doi:10.1111/j.1474-9726.2011.00759.x · Cited by 154 · see citing works
NK Cells in Healthy Aging and Age-Associated Diseases
Camous, X., Pera, A., Solana, R., & Larbi, A. (2012) · BioMed Research International · doi:10.1155/2012/195956 · Cited by 154 · see citing works
Functional dysregulation of stem cells during aging: a focus on skeletal muscle stem cells
García‐Prat, L., Sousa‐Victor, P., & Muñoz‐Cánoves, P. (2013) · The FEBS Journal · doi:10.1111/febs.12221 · Cited by 152 · see citing works
Qian, F., Wang, X., Zhang, L., Lin, A., Zhao, H., Fikrig, E., & Montgomery, R. R. (2011) · The Journal of Infectious Diseases · doi:10.1093/infdis/jir048 · Cited by 151 · see citing works
Martinez, C. O., McHale, M. J., Wells, J. T., Ochoa, O., Michalek, J. E., McManus, L. M., & Shireman, P. K. (2010) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00797.2009 · Cited by 151 · see citing works
Bencze, M., Négroni, E., Vallese, D., Yacoub‐Youssef, H., Chaouch, S., Wolff, A., Aamiri, A., Santo, J. P. D., Chazaud, B., Butler-Browne, G. S., et al. (2012) · Molecular Therapy · doi:10.1038/mt.2012.189 · Cited by 151 · see citing works
Role of CC chemokines in skeletal muscle functional restoration after injury
Warren, G. L., O’Farrell, L., Summan, M., Hulderman, T., Mishra, D., Luster, M. I., Kuziel, W. A., & Simeonova, P. P. (2004) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00467.2003 · Cited by 149 · see citing works
Cellular and Molecular Basis of Age-Related Sarcopenia
Welle, S. L. (2002) · Canadian Journal of Applied Physiology · doi:10.1139/h02-002 · Cited by 145 · see citing works
Ottnad, E., Parthasarathy, S., Sambrano, G. R., Ramprasad, M. P., Quehenberger, O., Kondratenko, N., Green, S., & Steinberg, D. H. (1995) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.92.5.1391 · Cited by 144 · see citing works
Clearance of Neutrophil-derived Myeloperoxidase by the Macrophage Mannose Receptor
Shepherd, V. L., & Hoidal, J. R. (1990) · American Journal of Respiratory Cell and Molecular Biology · doi:10.1165/ajrcmb/2.4.335 · Cited by 143 · see citing works
Replicative aging down‐regulates the myogenic regulatory factors in human myoblasts
Bigot, A., Jacquemin, V., Debacq‐Chainiaux, F., Butler-Browne, G. S., Toussaint, O., Furling, D., & Mouly, V. (2008) · Biology of the Cell · doi:10.1042/bc20070085 · Cited by 141 · see citing works
Barnard, W., Bower, J., Brown, M. A., Murphy, M., & Austin, L. (1994) · Journal of the Neurological Sciences · doi:10.1016/0022-510x(94)90211-9 · Cited by 140 · see citing works
Aging increases the susceptibility of skeletal muscle derived satellite cells to apoptosis
Jejurikar, S. S., Henkelman, E., Cederna, P. S., Marcelo, C. L., Urbanchek, M. G., & Kuzon, W. M. (2006) · Experimental Gerontology · doi:10.1016/j.exger.2006.06.053 · Cited by 133 · see citing works
Macrophage invasion does not contribute to muscle membrane injury during inflammation
Tidball, J., Berchenko, E., & Frenette, J. (1999) · Journal of Leukocyte Biology · doi:10.1002/jlb.65.4.492 · Cited by 132 · see citing works
NF-κB signaling in skeletal muscle: prospects for intervention in muscle diseases
Mourkioti, F., & Rosenthal, N. A. (2008) · Journal of Molecular Medicine · doi:10.1007/s00109-008-0308-4 · Cited by 132 · see citing works
Requirement of Inducible Nitric Oxide Synthase for Skeletal Muscle Regeneration after Acute Damage
Rigamonti, E., Touvier, T., Clementi, E., Manfredi, A. A., Brunelli, S., & Rovere, P. Q. (2013) · The Journal of Immunology · doi:10.4049/jimmunol.1202903 · Cited by 129 · see citing works
Barker, T., Henriksen, V. T., Martins, T. B., Hill, H. R., Kjeldsberg, C. R., Schneider, E. D., Dixon, B., & Weaver, L. K. (2013) · Nutrients · doi:10.3390/nu5041253 · Cited by 129 · see citing works
Radley‐Crabb, H. G., & Grounds, M. D. (2006) · Neurobiology of Disease · doi:10.1016/j.nbd.2006.03.016 · Cited by 129 · see citing works
Age-dependent alteration in muscle regeneration: the critical role of tissue niche
Barberi, L., Scicchitano, B. M., Rossi, M. D., Bigot, A., Duguez, S., Wielgosik, A., Stewart, C., McPhee, J., Conte, M., Narici, M., et al. (2013) · Biogerontology (Dordrecht) · doi:10.1007/s10522-013-9429-4 · Cited by 128 · see citing works
Zhang, J., Xiao, Z., Qu, C., Cui, W., Wang, X., & Du, J. (2014) · The Journal of Immunology · doi:10.4049/jimmunol.1303486 · Cited by 127 · see citing works
Martinis, M. D., Modesti, M., & Ginaldi, L. (2004) · Immunology and Cell Biology · doi:10.1111/j.0818-9641.2004.01242.x · Cited by 127 · see citing works
Skeletal Muscle Stem Cells: Effects of Aging and Metabolism on Muscle Regenerative FunctionPreprint
Jang, Y. C., Sinha, M., Cerletti, M., Dall’Osso, C., & Wagers, A. J. (2011) · Cold Spring Harbor Symposia on Quantitative Biology · doi:10.1101/sqb.2011.76.010652 · Cited by 127 · see citing works
Cantini, M., Giurisato, E., Radu, C. M., Tiozzo, S., Pampinella, F., Senigaglia, D., Zaniolo, G., Mazzoleni, F., & Vitiello, L. (2002) · Neurological Sciences · doi:10.1007/s100720200060 · Cited by 127 · see citing works
Nguyen, H. X., & Tidball, J. G. (2003) · The Journal of Physiology · doi:10.1113/jphysiol.2002.031450 · Cited by 122 · see citing works
Arthur, S. T., & Cooley, I. D. (2012) · International Journal of Biological Sciences · doi:10.7150/ijbs.4262 · Cited by 119 · see citing works
Lira, S. A., Zalamea, P., Heinrich, J. N., Fuentes, M. E., Carrasco, D., Lewin, A. C., Barton, D. S., Durham, S., & Bravo, R. (1994) · The Journal of experimental medicine · doi:10.1084/jem.180.6.2039 · Cited by 115 · see citing works
Hoene, M., Runge, H., Häring, H. U., Schleicher, E. D., & Weigert, C. (2013) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00025.2012 · Cited by 110 · see citing works
Evolving Therapeutic Strategies for Duchenne Muscular Dystrophy: Targeting Downstream Events
Tidball, J. G., & Wehling‐Henricks, M. (2004) · Pediatric Research · doi:10.1203/01.pdr.0000145578.01985.d0 · Cited by 108 · see citing works
Complement activation promotes muscle inflammation during modified muscle use.
Frenette, J., Cai, B.-Y., & Tidball, J. (2000) · American Journal of Pathology · doi:10.1016/s0002-9440(10)65081-x · Cited by 108 · see citing works
Choi, M., Park, H., Cho, S., & Lee, M. (2013) · Cytokine · doi:10.1016/j.cyto.2013.03.018 · Cited by 107 · see citing works
Magee, P., Pearson, S., & Allen, J. (2008) · Lipids in Health and Disease · doi:10.1186/1476-511x-7-24 · Cited by 105 · see citing works
Age-related skeletal muscle dysfunction: causes and mechanisms.
Degens, H. (2007) · PubMed · Cited by 103 · see citing works
Effect of exercise training on skeletal muscle cytokine expression in the elderly
Gatta, P. A. D., GARNHAM, A. P., Peake, J. M., & Cameron‐Smith, D. (2014) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2014.01.006 · Cited by 101 · see citing works
Leukaemia inhibitory factor - an exercise-induced myokine
Broholm, C., & Pedersen, B. K. (2026) · PubMed · doi:10.22029/eir.2010.1652 · Cited by 97 · see citing works
Tumor Necrosis Factor-α (TNF-α) Stimulates Chemotactic Response in Mouse Myogenic Cells
Torrente, Y., Fahime, E. E., Caron, N. J., Del Bo, R., Belicchi, M., Pisati, F., Tremblay, J. P., & Bresolin, N. (2003) · Cell Transplantation · doi:10.3727/000000003783985115 · Cited by 97 · see citing works
Early Life Nutrition Modulates Muscle Stem Cell Number: Implications for Muscle Mass and Repair
Woo, M., ISGANAITIS, E. M., Cerletti, M., Fitzpatrick, C., Wagers, A. J., Jimenez-Chillaron, J., & Patti, M. (2011) · Stem Cells and Development · doi:10.1089/scd.2010.0349 · Cited by 97 · see citing works
Effect of Inflammation on the Aging Microcirculation: Impact on Skeletal Muscle Blood Flow Control
Payne, G. W. (2006) · Microcirculation · doi:10.1080/10739680600618918 · Cited by 96 · see citing works
Wehling‐Henricks, M., Sokolow, S., Lee, J. J., Myung, K. H., Villalta, S. A., & Tidball, J. G. (2008) · Human Molecular Genetics · doi:10.1093/hmg/ddn129 · Cited by 96 · see citing works
Myoblasts produce IL-6 in response to inflammatory stimuli
Gallucci, S. (1998) · International Immunology · doi:10.1093/intimm/10.3.267 · Cited by 88 · see citing works
Null Mutation of gp91phox Reduces Muscle Membrane Lysis During Muscle Inflammation in Mice
Nguyen, H. X., & Tidball, J. (2003) · Journal of Physiology · doi:10.1113/jphysiol.2003.051912 · Cited by 87 · see citing works
Stratos, I., Li, Z., Herlyn, P. K. E., Rotter, R., Behrendt, A.-K., Mittlmeier, T., & Vollmar, B. (2012) · American Journal Of Pathology · doi:10.1016/j.ajpath.2012.11.006 · Cited by 84 · see citing works
CHARGÉ, S. B. P., Brack, A. S., & Hughes, S. M. (2002) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00206.2002 · Cited by 84 · see citing works
Age-related changes in the mitotic and metabolic characteristics of muscle-derived cells
Barani, A. E., Durieux, A., Sabido, O., & Freyssenet, D. G. (2003) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00437.2003 · Cited by 81 · see citing works
Increased myogenic repressor Id mRNA and protein levels in hindlimb muscles of aged rats
Alway, S. E., Degens, H., Lowe, D. A., & Krishnamurthy, G. (2002) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00332.2001 · Cited by 81 · see citing works
Akataki, K., Mita, K., Itoh, K., Suzuki, N., & Watakabe, M. (1996) · Muscle & Nerve · doi:10.1002/(sici)1097-4598(199610)19:10 · Cited by 81 · see citing works
Farup, J., Rahbek, S. K., Knudsen, I. S., de Paoli, F. V., Mackey, A. L., & Vissing, K. (2014) · Amino Acids · doi:10.1007/s00726-014-1810-3 · Cited by 78 · see citing works
Leucine Supplementation Improves Skeletal Muscle Regeneration after Cryolesion in Rats
Pereira, M. G., Baptista, I. L., Carlassara, E. O. C., Moriscot, A. S., Aoki, M. S., & Miyabara, E. H. (2014) · PLoS ONE · doi:10.1371/journal.pone.0085283 · Cited by 77 · see citing works
Domingues-Faria, C., Chanet, A., Salles, J., Berry, A., Giraudet, C., Patrac, V., Denis, P., Bouton, K., Gonçalves-Mendes, N., Vasson, M., et al. (2014) · Nutrition & Metabolism · doi:10.1186/1743-7075-11-47 · Cited by 77 · see citing works
Nguyen, H. X., Lusis, A., & Tidball, J. (2005) · Journal of Physiology · doi:10.1113/jphysiol.2005.085506 · Cited by 75 · see citing works
Regenerative capacity of skeletal muscle
Ehrhardt, J., & Morgan, J. E. (2005) · Current Opinion in Neurology · doi:10.1097/01.wco.0000177382.62156.82 · Cited by 72 · see citing works
Evans, N. P., Call, J. A., Bassaganya-Riera, J., Robertson, J. L., & Grange, R. W. (2009) · Clinical Nutrition · doi:10.1016/j.clnu.2009.10.001 · Cited by 66 · see citing works
Immunosenescence, Aging, and Systemic Lupus Erythematous
Montoya-Ortiz, G. (2013) · Autoimmune Diseases · doi:10.1155/2013/267078 · Cited by 65 · see citing works
Accelerated skeletal muscle recovery after in vivo polyphenol administration
Myburgh, K. H., Kruger, M. J., & Smith, C. (2011) · The Journal of Nutritional Biochemistry · doi:10.1016/j.jnutbio.2011.05.014 · Cited by 63 · see citing works
Age‐Dependent Effects on Functional Aspects in Human Satellite Cells
BECCAFICO, S., PUGLIELLI, C., PIETRANGELO, T., BELLOMO, R., FANÒ, G., & FULLE, S. (2007) · Annals of the New York Academy of Sciences · doi:10.1196/annals.1395.037 · Cited by 61 · see citing works
Lesault, P., Théret, M., Magnan, M., Cuvellier, S., Niu, Y., Gherardi, R. K., Tremblay, J. P., Hittinger, L., & Chazaud, B. (2012) · PLoS ONE · doi:10.1371/journal.pone.0046698 · Cited by 61 · see citing works
Aging and Marrow Neutrophil Reserves
Chatta, G. S., Price, T. H., Stratton, J. R., & Dale, D. C. (1994) · Journal of the American Geriatrics Society · doi:10.1111/j.1532-5415.1994.tb06077.x · Cited by 60 · see citing works
Age-associated decrease in muscle precursor cell differentiation
Lees, S. J., Rathbone, C. R., & Booth, F. W. (2005) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00408.2005 · Cited by 58 · see citing works
STAT3 induces muscle stem cell differentiation by interaction with myoD
Yang, Y., Xu, Y., Li, W., Wang, G., Song, Y., Yang, G., Han, X., Du, Z., Sun, L., & Ma, K. (2009) · Cytokine · doi:10.1016/j.cyto.2008.12.015 · Cited by 54 · see citing works
Zádor, E., Mendler, L., Takács, V., Bleecker, J. D., & Wuytack, F. (2001) · Muscle & Nerve · doi:10.1002/mus.1110 · Cited by 51 · see citing works
Proapoptotic factor Bax is increased in satellite cells in the tibialis anterior muscles of old rats
Krajnak, K., Waugh, S., Miller, R., Baker, B. A., Geronilla, K. B., Alway, S. E., & Cutlip, R. G. (2006) · Muscle & Nerve · doi:10.1002/mus.20656 · Cited by 46 · see citing works
Blomberg, B. B., Frasca, D., Diaz, A., & Antoni, M. (2023) · The Journal of Immunology · doi:10.4049/jimmunol.210.supp.88.13 · Cited by 45 · see citing works
Barker, T., Martins, T. B., Hill, H. R., Kjeldsberg, C. R., Dixon, B. M., Schneider, E. D., Henriksen, V. T., & Weaver, L. K. (2014) · Cytokine · doi:10.1016/j.cyto.2013.12.004 · Cited by 43 · see citing works
Age-related responses of the microcirculation to ischemia-reperfusion and inflammation
Harris, N. R., & Rumbaut, R. E. (2001) · Pathophysiology · doi:10.1016/s0928-4680(01)00064-5 · Cited by 41 · see citing works
Leucine Supplementation Accelerates Connective Tissue Repair of Injured Tibialis Anterior Muscle
Pereira, M. G., da Silva, M. T., Carlassara, E. O. C., Gonçalves, D. A. P., Abrahamsohn, P. A., Kettelhut, Í. D. C., Moriscot, A. S., Aoki, M. S., & Miyabara, E. H. (2014) · Nutrients · doi:10.3390/nu6103981 · Cited by 35 · see citing works
Vasson, M., Farges, M., Gonçalves-Mendes, N., Talvas, J., Ribalta, J., Winklhofer‐Roob, B. M., Rock, E., & Rossary, A. (2013) · Immunity & Ageing · doi:10.1186/1742-4933-10-38 · Cited by 30 · see citing works
Age-related impairment of T cell-induced skeletal muscle precursor cell function
Dumke, B. R., & Lees, S. J. (2011) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00354.2010 · Cited by 30 · see citing works
Beneficial effects of cod protein on skeletal muscle repair following injury
Dort, J., Sirois, A., Leblanc, N., Côt́e, C. H., & Jacques, H. (2012) · Applied Physiology, Nutrition, and Metabolism · doi:10.1139/h2012-021 · Cited by 29 · see citing works
Zerria, K., Jerbi, E., Hammami, S., Maaroufi, A., Boubaker, S., Xiong, J.-P., Arnaout, M. A., & Fathallah, D. M. (2006) · Immunology · doi:10.1111/j.1365-2567.2006.02454.x · Cited by 24 · see citing works
Rejuvenating aged muscle stem cells
Bentzinger, C. F., & Rudnicki, M. A. (2014) · Nature Medicine · doi:10.1038/nm.3499 · Cited by 24 · see citing works
Dort, J., Leblanc, N., Maltais‐Giguère, J., Liaset, B., Côt́e, C. H., & Jacques, H. (2013) · PLoS ONE · doi:10.1371/journal.pone.0077274 · Cited by 22 · see citing works
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Li, Y., Xiao, Y., & Liu, C. (2017) · Chemical Reviews · doi:10.1021/acs.chemrev.6b00654 · Cited by 600 · see citing works
Sarcopenia – Molecular mechanisms and open questions
Wiedmer, P., Jung, T., Castro, J. P., Pomatto, L. C. D., Sun, P. Y., Davies, K. J. A., & Grune, T. (2020) · Ageing Research Reviews · doi:10.1016/j.arr.2020.101200 · Cited by 476 · see citing works
Skeletal Muscle as Potential Central Link between Sarcopenia and Immune Senescence
Nelke, C., Dziewas, R., Minnerup, J., Meuth, S. G., & Ruck, T. (2019) · eBioMedicine · doi:10.1016/j.ebiom.2019.10.034 · Cited by 437 · see citing works
Impact of the Natural Compound Urolithin A on Health, Disease, and Aging
D'Amico, D. F., Andreux, P. A., Valdés, P., Singh, A., Rinsch, C., & Auwerx, J. H. (2021) · Trends in Molecular Medicine · doi:10.1016/j.molmed.2021.04.009 · Cited by 417 · see citing works
Bilski, J., Pierzchalski, P., Szczepanik, M., Bonior, J., & Zoladz, J. A. (2022) · Cells · doi:10.3390/cells11010160 · Cited by 262 · see citing works
Advances in muscle health and nutrition: A toolkit for healthcare professionals
Prado, C. M., Landi, F., Chew, S. T. H., Atherton, P. J., Molinger, J., Ruck, T., & Gonzalez, M. C. (2022) · Clinical Nutrition · doi:10.1016/j.clnu.2022.07.041 · Cited by 237 · see citing works
Eivazzadeh‐Keihan, R., Chenab, K. K., Taheri‐Ledari, R., Mosafer, J., Hashemi, S. M., Mokhtarzadeh, A., Maleki, A. R., & Hamblin, M. R. (2019) · Materials Science and Engineering C · doi:10.1016/j.msec.2019.110267 · Cited by 201 · see citing works
Fang, E. F., Waltz, T. B., Kassahun, H., Lu, Q., Kerr, J. S., Morevati, M., Fivenson, E. M., Wollman, B. N., Marosi, K., Wilson, M. A., et al. (2017) · Scientific Reports · doi:10.1038/srep46208 · Cited by 187 · see citing works
Santa, F. D., Vitiello, L., Torcinaro, A., & Ferraro, E. (2018) · Antioxidants and Redox Signaling · doi:10.1089/ars.2017.7420 · Cited by 154 · see citing works
LIM, C., NUNES, E. A., CURRIER, B. S., MCLEOD, J. C., THOMAS, A. C. Q., & PHILLIPS, S. M. (2022) · Medicine & Science in Sports & Exercise · doi:10.1249/mss.0000000000002929 · Cited by 142 · see citing works
Nanomaterial-based bone regeneration
Li, Y., & Liu, C. (2017) · Nanoscale · doi:10.1039/c7nr00835j · Cited by 122 · see citing works
Liu, Y., Weng, W., Gao, R., & Liu, Y. (2019) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2019/4598167 · Cited by 116 · see citing works
Potential Roles of n-3 PUFAs during Skeletal Muscle Growth and Regeneration
Tachtsis, B., Camera, D., & Lacham-Kaplan, O. (2018) · Nutrients · doi:10.3390/nu10030309 · Cited by 104 · see citing works
Govoni, A., Gagliardi, D., Comi, G. P., & Corti, S. P. (2018) · Molecular Neurobiology · doi:10.1007/s12035-017-0831-9 · Cited by 86 · see citing works
Mediterranean Diet and Quality of Life in Adults: A Systematic Review
Godos, J., Guglielmetti, M., Ferraris, C., Frías-Toral, E., Azpíroz, I. D., Lipari, V., Mauro, A. D., Furnari, F., Castellano, S., Galvano, F., et al. (2025) · Nutrients · doi:10.3390/nu17030577 · Cited by 94 · see citing works
Low vitamin intake is associated with risk of frailty in older adults
Balboa‐Castillo, T., Struijk, E. A., López‐García, E., Banegas, J. R., Rodríguez‐Artalejo, F., & Guallar‐Castillón, P. (2018) · Age and Ageing · doi:10.1093/ageing/afy105 · Cited by 79 · see citing works
Álvarez, Á. M., DeOcesano-Pereira, C., Teixeira, C., & Moreira, V. (2020) · Cells · doi:10.3390/cells9092005 · Cited by 78 · see citing works
Autophagy in muscle regeneration: potential therapies for myopathies
Chen, W., Chen, Y., Liu, Y., & Wang, X. (2022) · Journal of Cachexia Sarcopenia and Muscle · doi:10.1002/jcsm.13000 · Cited by 77 · see citing works
Contribution of muscle satellite cells to sarcopenia
Huo, F., Liu, Q., & Liu, H. (2022) · Frontiers in Physiology · doi:10.3389/fphys.2022.892749 · Cited by 74 · see citing works
Graça, F. A., Stephan, A., Minden‐Birkenmaier, B. A., Shirinifard, A., Wang, Y., Demontis, F., & Labelle, M. (2023) · Nature Communications · doi:10.1038/s41467-023-38624-0 · Cited by 73 · see citing works
Agoncillo, M., Yu, J., & Gunton, J. E. (2023) · Nutrients · doi:10.3390/nu15204377 · Cited by 64 · see citing works
Schoufour, J. D., Tieland, M., Barazzoni, R., Ben Allouch, S., Bie, J. V. D., Boirie, Y., Cruz-Jentoft, A. J., Eglseer, D., Topinková, E., Visser, B., et al. (2021) · Frontiers in Nutrition · doi:10.3389/fnut.2021.661449 · Cited by 62 · see citing works
Jannas-Vela, S., Espinosa, A., Candia, A. A., Flores‐Opazo, M., Peñailillo, L., & Valenzuela, R. (2023) · Nutrients · doi:10.3390/nu15040871 · Cited by 61 · see citing works
Vennekens, A., Laporte, E., Hermans, F., Cox, B., Modave, E., Janiszewski, A., Nys, C., Kobayashi, H., Malengier‐Devlies, B., Chappell, J., et al. (2021) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2100052118 · Cited by 59 · see citing works
Single-nucleus profiling unveils a geroprotective role of the FOXO3 in primate skeletal muscle aging
Jing, Y., Zuo, Y., Yu, Y., Sun, L., Yu, Z., Ma, S., Zhao, Q., Sun, G., Hu, H., Li, J., et al. (2022) · Protein & Cell · doi:10.1093/procel/pwac061 · Cited by 57 · see citing works
Mechanisms of muscle cells alterations and regeneration decline during aging
Chinvattanachot, G., Rivas, D., & Duque, G. (2024) · Ageing Research Reviews · doi:10.1016/j.arr.2024.102589 · Cited by 58 · see citing works
Drosophila muscles regulate the immune response against wasp infection via carbohydrate metabolism
Yang, H., & Hultmark, D. (2017) · Scientific Reports · doi:10.1038/s41598-017-15940-2 · Cited by 55 · see citing works
Immunometabolism: Insights from the Drosophila model
Galenza, A., & Foley, E. (2019) · Developmental & Comparative Immunology · doi:10.1016/j.dci.2019.01.011 · Cited by 52 · see citing works
“English Disease”: Historical Notes on Rickets, the Bone–Lung Link and Child Neglect Issues
Zhang, M.-Y., Shen, F., Petryk, A., Tang, J., Chen, X., & Sergi, C. M. (2016) · Nutrients · doi:10.3390/nu8110722 · Cited by 51 · see citing works
Anderson, J. E. (2021) · European Journal of Applied Physiology · doi:10.1007/s00421-021-04865-4 · Cited by 52 · see citing works
Roles of the fibroblast growth factor signal transduction system in tissue injury repair
Chen, K., Rao, Z., Dong, S., Chen, Y., Wang, X., Luo, Y., Gong, F., & Li, X. (2022) · Burns & Trauma · doi:10.1093/burnst/tkac005 · Cited by 49 · see citing works
Acute Sarcopenia: Mechanisms and Management
Damanti, S., Senini, E., LORENZO, R. D., Merolla, A., Santoro, S., Festorazzi, C., Messina, M., Vitali, G., Sciorati, C., & Rovere, P. Q. (2024) · Nutrients · doi:10.3390/nu16203428 · Cited by 50 · see citing works
MuSCs and IPCs: roles in skeletal muscle homeostasis, aging and injury
Jiang, H., Liu, B., Lin, J., Xue, T., Han, Y., Lu, C., Zhou, S., Gu, Y., Xu, F., Shen, Y., et al. (2024) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-023-05096-w · Cited by 46 · see citing works
Go, G.-Y., Jo, A., Seo, D.-W., Kim, W.-Y., Kim, Y. K., So, E.-Y., Chen, Q., Kang, J.-S., Bae, G.-U., & Lee, S.-J. (2020) · Journal of Ginseng Research · doi:10.1016/j.jgr.2019.01.007 · Cited by 45 · see citing works
Cochet, C., Belloni, G., Buondonno, I., Chiara, F., & D’Amelio, P. (2023) · Nutrients · doi:10.3390/nu15173703 · Cited by 44 · see citing works
Tallis, J. A., Shelley, S. P., Degens, H., & Hill, C. (2021) · Biomolecules · doi:10.3390/biom11030372 · Cited by 44 · see citing works
Impact of Western and Mediterranean Diets and Vitamin D on Muscle Fibers of Sedentary Rats
Trovato, F. M., Castrogiovanni, P., Szychlinska, M. A., Purrello, F., & Musumeci, G. (2018) · Nutrients · doi:10.3390/nu10020231 · Cited by 41 · see citing works
Age-Related Changes in the Matrisome of the Mouse Skeletal Muscle
Lofaro, F. D., Cisterna, B., Lacavalla, M. A., Boschi, F., Malatesta, M., Quaglino, D., Zancanaro, C., & Boraldi, F. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms221910564 · Cited by 40 · see citing works
Tu, S., Hao, X., Xu, S., Jin, X., Liao, W., Xia, H., Wang, S., & Sun, G. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms26146740 · Cited by 35 · see citing works
Huang, K., Cai, H., Bao, J., & Wu, L. (2020) · Ageing Research Reviews · doi:10.1016/j.arr.2020.101132 · Cited by 36 · see citing works
Natural products and skeletal muscle health
Qu, Z., Zhou, S., Li, P., Liu, C., Yuan, B., Zhang, S., & Liu, A. (2021) · The Journal of Nutritional Biochemistry · doi:10.1016/j.jnutbio.2021.108619 · Cited by 35 · see citing works
Barbiera, A., Sorrentino, S., Fard, D., Lepore, E., Sica, G., Dobrowolny, G., Tamagnone, L., & Scicchitano, B. M. (2022) · Antioxidants · doi:10.3390/antiox11051016 · Cited by 35 · see citing works
Tu, H., Zhang, D., Corrick, R. M., Muelleman, R. L., Wadman, M. C., & Li, Y. (2017) · Frontiers in Physiology · doi:10.3389/fphys.2017.00207 · Cited by 33 · see citing works
Mullen, M. T., Williams, K. B., LaRocca, T. J., Duke, V. R., Hambright, W. S., Ravuri, S. K., Bahney, C. S., Ehrhart, N. P., & Huard, J. (2022) · Journal of Orthopaedic Research® · doi:10.1002/jor.25467 · Cited by 32 · see citing works
Wu, D., Gao, X., Shi, Y., Wang, H., Wang, W., Li, Y., & Zheng, Z. (2022) · International Journal of Environmental Research and Public Health · doi:10.3390/ijerph192013616 · Cited by 32 · see citing works
Nuñez-Lisboa, M., Valero‐Breton, M., & Dewolf, A. H. (2023) · Frontiers in Physiology · doi:10.3389/fphys.2023.1194889 · Cited by 24 · see citing works
Mitochondrial transplantation as a possible therapeutic option for sarcopenia
Türkel, İ., Özerkliğ, B., Yılmaz, M., Ülger, Ö., Kubat, G. B., & Tuncer, M. (2023) · Journal of Molecular Medicine · doi:10.1007/s00109-023-02326-3 · Cited by 24 · see citing works
Wang, T., Xu, H. Y., Wu, S., Guo, Y., Zhao, G., & Wang, D. (2023) · Journal of Agricultural and Food Chemistry · doi:10.1021/acs.jafc.3c02023 · Cited by 27 · see citing works
Comprehensive Analytics of Actovegin® and Its Effect on Muscle Cells
Reichl, F., Holdt, L. M., Teupser, D., Schütze, G. A., Metcalfe, A., Hickel, R., Högg, C., & Bloch, W. (2017) · International Journal of Sports Medicine · doi:10.1055/s-0043-115738 · Cited by 24 · see citing works
Dietary supplement intake among the elderly
Walrand, S. (2018) · Current Opinion in Clinical Nutrition & Metabolic Care · doi:10.1097/mco.0000000000000512 · Cited by 24 · see citing works
Soerensen, M., Li, W., Debrabant, B., Nygaard, M., Mengel‐From, J., Frost, M., Christensen, K., Christiansen, L., & Tan, Q. (2019) · Biogerontology · doi:10.1007/s10522-019-09818-1 · Cited by 23 · see citing works
Malila, Y., Uengwetwanit, T., Thanatsang, K. V., Arayamethakorn, S., Srimarut, Y., Petracci, M., Soglia, F., Rungrassamee, W., & Visessanguan, W. (2021) · Frontiers in Physiology · doi:10.3389/fphys.2021.691194 · Cited by 23 · see citing works
Regenerative Repair of Volumetric Muscle Loss Injury is Sensitive to Age
Kim, J. T., Kasukonis, B. M., Dunlap, G., Perry, R. A., Washington, T. A., & Wolchok, J. C. (2019) · Tissue Engineering Part A · doi:10.1089/ten.tea.2019.0034 · Cited by 23 · see citing works
Dual effects of obesity on satellite cells and muscle regeneration
Geiger, A. E., Daughtry, M. R., Yen, C., Kirkpatrick, L. T., Shi, H., & Gerrard, D. E. (2020) · Physiological Reports · doi:10.14814/phy2.14511 · Cited by 21 · see citing works
Qu, Z., Liu, C., Li, P., Xiong, W., Zeng, Z., Liu, A., Xiao, W., Huang, J., Liu, Z., & Zhang, S. (2020) · Journal of Agricultural and Food Chemistry · doi:10.1021/acs.jafc.0c03744 · Cited by 22 · see citing works
Ersoy, U., Kanakis, I., Alameddine, M., Pedraza-Vázquez, G., Ozanne, S. E., Peffers, M. J., Jackson, M. J., Goljanek‐Whysall, K., & Vasilaki, A. (2023) · Redox Biology · doi:10.1016/j.redox.2023.102980 · Cited by 22 · see citing works
Gold nanoparticles modulate macrophage polarization to promote skeletal muscle regeneration
Xu, L., Qiu, J., Ren, Q., Wang, D., Guo, A., Wang, L., Hou, K., Wang, R., & Liu, Y. (2025) · Materials Today Bio · doi:10.1016/j.mtbio.2025.101653 · Cited by 21 · see citing works
Using polyphenol derivatives to prevent muscle wasting
Francaux, M., & Deldicque, L. (2018) · Current Opinion in Clinical Nutrition & Metabolic Care · doi:10.1097/mco.0000000000000455 · Cited by 21 · see citing works
Ginsenoside Rg5 promotes muscle regeneration via p38MAPK and Akt/mTOR signaling
Kim, R., Kim, J. W., Choi, H., Oh, J., Kim, T. H., Go, G.-Y., Lee, S.-J., & Bae, G. (2023) · Journal of Ginseng Research · doi:10.1016/j.jgr.2023.06.004 · Cited by 21 · see citing works
nNOS/GSNOR interaction contributes to skeletal muscle differentiation and homeostasis
Montagna, C., Rizza, S., Cirotti, C., Maiani, E., Muscaritoli, M., Musarò, A., Carrı̀, M. T., Ferraro, E., Cecconi, F., & Filomeni, G. (2019) · Cell Death and Disease · doi:10.1038/s41419-019-1584-3 · Cited by 21 · see citing works
Malila, Y., Thanatsang, K. V., Sanpinit, P., Arayamethakorn, S., Soglia, F., Zappaterra, M., Bordini, M., Sirri, F., Rungrassamee, W., Davoli, R., et al. (2022) · PLoS ONE · doi:10.1371/journal.pone.0275160 · Cited by 20 · see citing works
Chang, S.-S., Chen, L., Huang, K., Huang, S.-W., Chang, C., Liao, K., Hu, E.-C., Chen, Y., Chen, Y., Hsu, P.-C., et al. (2023) · Food & Function · doi:10.1039/d3fo02766j · Cited by 20 · see citing works
Immune Cells and Immunosenescence
Bischof, J., Gärtner, F., Zeiser, K., Kunz, R., Schreiner, C., Hoffer, E., Burster, T., Knippschild, U., & Zimecki, M. (2019) · Folia Biologica · doi:10.14712/fb2019065020053 · Cited by 18 · see citing works
van Santen, V. J. B., Klein‐Nulend, J., Bakker, A. D., & Jaspers, R. T. (2022) · Cell Biochemistry and Biophysics · doi:10.1007/s12013-021-01050-4 · Cited by 17 · see citing works
Abreu, P., Pinheiro, C. H. D. J., Vitzel, K. F., de Vasconcelos, D. A. A., Torres, R. P., Fortes, M. A. S., Marzuca-Nassr, G. N., Mancini‐Filho, J., Hirabara, S. M., & Curi, R. (2016) · Experimental Physiology · doi:10.1113/ep085899 · Cited by 16 · see citing works
Serum vitamin D status and circulating irisin levels in older adults with sarcopenia
Wang, Y., Gu, Y., Huang, J. H., Wu, H., Meng, G., Zhang, Q., Liu, L., Zhang, S., Wang, X., Zhang, J., et al. (2022) · Frontiers in Nutrition · doi:10.3389/fnut.2022.1051870 · Cited by 16 · see citing works
Exercise, circadian rhythms, and muscle regeneration: a path to healthy aging
Su, Z., & Xiang, L. (2025) · Frontiers in Neuroscience · doi:10.3389/fnins.2025.1633835 · Cited by 15 · see citing works
RetractedXu, L., Zhang, Y., Wang, D., Ren, Q., Wang, Y., Zang, Z., Guo, A., Guo, J., Wang, L., Wang, R., et al. (2025) · Small · doi:10.1002/smll.202412611 · Cited by 14 · see citing works
A simple model of immune and muscle cell crosstalk during muscle regeneration
Kojouharov, H. V., Chen‐Charpentier, B. M., Solís, F. J., Biguetti, C. C., & Brotto, M. A. P. (2021) · Mathematical Biosciences · doi:10.1016/j.mbs.2021.108543 · Cited by 14 · see citing works
Han, M.-J., Park, S.-J., Lee, S., & Choung, S. (2022) · Nutrients · doi:10.3390/nu14040799 · Cited by 14 · see citing works
Brabcová, I., Trešlová, M., Bártlová, S., Vacková, J., Tóthová, V., & Motlová, L. (2016) · Central European Journal of Public Health · doi:10.21101/cejph.a4283 · Cited by 14 · see citing works
Chen, S., Zhang, S., Zheng, Q., Miao, J., & Guo, J. (2025) · PLoS ONE · doi:10.1371/journal.pone.0318920 · Cited by 13 · see citing works
Valenzuela, C., Azúa, M., Álvarez, C., Schmitt, P., Ojeda, N., & Mercado, L. A. (2023) · Animals · doi:10.3390/ani13050880 · Cited by 13 · see citing works
Komaru, T., Yanaka, N., & Kumrungsee, T. (2021) · Nutrients · doi:10.3390/nu13124531 · Cited by 12 · see citing works
Márquez-Arabia, W. H., Gómez-Hoyos, J., Gómez, M. G., Flórez, I. D., Gallo‐Villegas, J., Monsalve, F. J., Arias, L. F., & Martin, H. D. (2017) · Arthroscopy The Journal of Arthroscopic and Related Surgery · doi:10.1016/j.arthro.2017.01.036 · Cited by 12 · see citing works
Oh, H., Jin, H., & Lee, B.-Y. (2022) · Journal of Ginseng Research · doi:10.1016/j.jgr.2022.05.007 · Cited by 12 · see citing works
Liposome‐Enabled Nanomaterials for Muscle Regeneration
Wu, S., & Lu, J. (2025) · Small Methods · doi:10.1002/smtd.202402154 · Cited by 11 · see citing works
Liu, S., Liu, H., Liu, Y., Zhang, J., Liu, Z., Zheng, Z., & Luo, E. (2022) · Cell Proliferation · doi:10.1111/cpr.13370 · Cited by 10 · see citing works
Mosele, F. C., Ricci, R. B., Abreu, P., & Neto, J. C. R. (2020) · Journal of Cellular Physiology · doi:10.1002/jcp.29547 · Cited by 11 · see citing works
Benlebna, M., Balas, L., Pessemesse, L., Bonafos, B., Fouret, G., Pavlin, L., Goustard, B., Gaillet, S., Durand, T., Coudray, C., et al. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21239046 · Cited by 11 · see citing works
Molecular mechanism of skeletal muscle loss and its prevention by natural resources
Kim, J. T., Jeon, D. H., & Lee, H. J. (2024) · Food Science and Biotechnology · doi:10.1007/s10068-024-01678-x · Cited by 10 · see citing works
Evaluating skeletal muscle wasting and weakness in models of critical illness
Bongetti, A. J., Caldow, M. K., Abdelhamid, Y. A., & Lynch, G. S. (2025) · Clinical Science · doi:10.1042/cs20255458 · Cited by 10 · see citing works
Soluble interleukin 2 receptor is risk for sarcopenia in Men with high fracture risk
Ge, J., Zeng, J., Li, N., Ma, H., Zhao, Z., Sun, S., Jing, Y., Qian, C., Fei, Z., Qu, S., et al. (2022) · Journal of Orthopaedic Translation · doi:10.1016/j.jot.2022.10.017 · Cited by 10 · see citing works
Age‐related nitration/dysfunction of myogenic stem cell activator HGF
Elgaabari, A., Imatomi, N., Kido, H., Nakashima, T., Okuda, S., Manabe, Y., Sawano, S., Mizunoya, W., Kaneko, R., Tanaka, S., et al. (2023) · Aging Cell · doi:10.1111/acel.14041 · Cited by 9 · see citing works
Insights into the epitranscriptomic role of N6-methyladenosine on aging skeletal muscle
Enechojo, O. S., Wang, J., Shi, Y., Wang, Y., Xu, Z., Abankwah, J. K., Pozzo, L. D., Zhao, S., Zhou, H., Peng, Y., et al. (2024) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2024.117041 · Cited by 9 · see citing works
Wang, Y., Chen, W., Wang, C., Li, L., Bi, B., Li, S., & Wu, H. (2025) · Journal of Cachexia Sarcopenia and Muscle · doi:10.1002/jcsm.70017 · Cited by 9 · see citing works
Relaño, M. L., Manyes, L., Peiró, J., & Ramada, J. M. (2018) · Nutrición Hospitalaria · doi:10.20960/nh.1946 · Cited by 9 · see citing works
Daneshvar, N., & Anderson, J. E. (2022) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2022.874756 · Cited by 8 · see citing works
Nguyen, B. N., Hong, S., Choi, S., Lee, C., Yoo, G., & Kim, M. (2023) · Journal of Ginseng Research · doi:10.1016/j.jgr.2023.12.004 · Cited by 7 · see citing works
Regenerative Engineering of a Limb: From Amputation to Regeneration
Abedini, A. A., Hosseini, F. S., & Laurencin, C. T. (2023) · Regenerative Engineering and Translational Medicine · doi:10.1007/s40883-023-00323-z · Cited by 8 · see citing works
Tipbunjong, C., Thitiphatphuvanon, T., Pholpramool, C., & Surinlert, P. (2024) · Journal of Toxicology · doi:10.1155/2024/3840950 · Cited by 7 · see citing works
Yang, M., Sun, L., Kawabata, Y., Murayama, F., Maegawa, T., Nikawa, T., & Hirasaka, K. (2022) · Marine Drugs · doi:10.3390/md20050313 · Cited by 9 · see citing works
Investigation of niclosamide as a repurposing agent for skeletal muscle atrophy
Kim, H., Lee, J., Kim, S.-W., Lee, S., Jung, D., & Williams, D. R. (2021) · PLoS ONE · doi:10.1371/journal.pone.0252135 · Cited by 7 · see citing works
Genomic stability and telomere regulation in skeletal muscle tissue
Trajano, L. A. D. S. N., Trajano, E. T. L., Silva, M. A. D. S., Stumbo, A. C., Mencalha, A. L., & da Fonseca, A. D. S. (2018) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2018.01.004 · Cited by 7 · see citing works
Role of l-carnitine and oleate in myogenic differentiation: implications for myofiber regeneration
Lee, H., Lim, J., & Choi, S.-J. (2018) · Physical Activity and Nutrition · doi:10.20463/jenb.2018.0015 · Cited by 7 · see citing works
Sarcopenia dan Risiko Jatuh pada Pasien Geriatri
Setiorini, A. (2021) · Muhammadiyah Journal of Geriatric · doi:10.24853/mujg.2.1.10-16 · Cited by 6 · see citing works
Sarcopenia predicts 5‐year mortality in older adults with intellectual disabilities
Valentin, B., Festen, D. A. M., Schoufour, J. D., & Oppewal, A. (2023) · Journal of Intellectual Disability Research · doi:10.1111/jir.13078 · Cited by 6 · see citing works
Effect of Lactobacillus curvatus HY7602-Fermented Antler on Sarcopenia in Mice
Jeon, H., Lee, K., Kim, J.-Y., Shim, J.-J., & Lee, J.-L. (2023) · Fermentation · doi:10.3390/fermentation9050429 · Cited by 5 · see citing works
Valente, J. S., Perez, E. S., Zanella, B. T. T., de Paula, T. G., dos Santos, S. A. A., Duran, B. O. D. S., Carvalho, R. F., Justulin, L. A., Fantinatti, B. E. A., & Dal‐Pai‐Silva, M. (2021) · PubMed · doi:10.14670/hh-18-337 · Cited by 5 · see citing works
Li, S., Ma, H., Wu, J., Lu, J., Qiao, S., Zeng, X., & Zhou, J. (2025) · Agriculture · doi:10.3390/agriculture15121306 · Cited by 4 · see citing works
- Authors
- Domingues-Faria, C., Vasson, M.-P., Goncalves-Mendes, N., Boirie, Y., & Walrand, S.
- Affiliations
- Université Clermont Auvergne (FR)
- ORCID
- Vasson, Marie-Paule
- Venue
- Ageing Research Reviews
- Publisher
- Elsevier BV
- Published
- 2016-03
- Volume
- 26
- Pages
- 22-36
- ISSN
- 1568-1637 (ISSN-L)
- OpenAlex
- W2193057007
- Cited by
- 157
- References
- 178
- Citations by year
- 2026: 8 · 2025: 21 · 2024: 17 · 2023: 21 · 2022: 22 · 2021: 18 · 2020: 12 · 2019: 10 · 2018: 14 · 2017: 8 · 2016: 6
- FWCI
- 0.91
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Ageing Research Reviews (publishedVersion)
- PubMed (publishedVersion)
- HAL (submittedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Muscle Physiology and Disorders
- Health Sciences › Medicine › Physiology › Nutrition and Health in Aging
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Muscle metabolism and nutrition
- Keywords
- skeletal muscle regeneration, muscle aging, sarcopenia, muscle stem cells, immune cells, nutrition, amino acids, omega-3 fatty acids, polyphenols, vitamin D, muscle injury repair
- MeSH terms
- Immunosenescence, Aging, Humans, Nutritional Status, Regeneration, Muscle Fibers, Skeletal, Sarcopenia
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