Potential role of omega-3 fatty acids on the myogenic program of satellite cells
Open accessAbstract
Skeletal muscle loss is associated with aging as well as pathological conditions. Satellite cells (SCs) play an important role in muscle regeneration. Omega-3 fatty acids are widely studied in a variety of muscle wasting diseases; however, little is known about their impact on skeletal muscle regeneration. The aim of this review is to evaluate studies examining the effect of omega-3 fatty acids, α-linolenic acid, eicosapentaenoic acid, and docosahexaenoic acid on the regulation of SC proliferation and differentiation. This review highlights mechanisms by which omega-3 fatty acids may modulate the myogenic program of the stem cell population within skeletal muscles and identifies considerations for future studies. It is proposed that minimally three myogenic transcriptional regulatory factors, paired box 7 (Pax7), myogenic differentiation 1 protein, and myogenin, should be measured to confirm the stage of SCs within the myogenic program affected by omega-3 fatty acids.
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
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?
n-3 PUFAs alter skeletal muscle function.
“and more recently alter skeletal muscle function”
From Potential Roles of n-3 PUFAs during Skeletal Muscle Growth and Regeneration (2018) · cites this paper as [48]
n-3 PUFAs may stimulate rates of muscle protein synthesis by increasing intracellular activities of signalling molecules involved in maintenance of skeletal muscle mass and possibly satellite cell activity.
“Accumulating evidence now indicates that n-3 PUFAs may additionally stimulate rates of muscle protein synthesis (MPS) by increasing both the intracellular activities of signalling molecules that are involved in the maintenance of skeletal muscle mass [46,47] and possibly satellite cell activity [48].”
From Potential Roles of n-3 PUFAs during Skeletal Muscle Growth and Regeneration (2018) · cites this paper as [48]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Cites
SATELLITE CELL OF SKELETAL MUSCLE FIBERS
Mauro, A. (1961) · The Journal of Cell Biology · doi:10.1083/jcb.9.2.493 · Cited by 3,683 · see citing works
Prado, C. M., Lieffers, J. R., McCargar, L. J., Reiman, T., Sawyer, M. B., Martin, L., & Baracos, V. E. (2008) · The Lancet Oncology · doi:10.1016/s1470-2045(08)70153-0 · Cited by 3,238 · see citing works
Martin, L., Birdsell, L., Macdonald, N., Reiman, T., Clandinin, M. T., McCargar, L. J., Murphy, R. A., Ghosh, S., Sawyer, M. B., & Baracos, V. E. (2013) · Journal of Clinical Oncology · doi:10.1200/jco.2012.45.2722 · Cited by 2,698 · 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
Pax7 Is Required for the Specification of Myogenic Satellite Cells
Seale, P., Sabourin, L. A., Girgis-Gabardo, A., Mansouri, A., Gruß, P., & Rudnicki, M. A. (2000) · Cell · doi:10.1016/s0092-8674(00)00066-0 · Cited by 2,345 · see citing works
Serial passaging and differentiation of myogenic cells isolated from dystrophic mouse muscle
Yaffe, D., & Saxel, O. (1977) · Nature · doi:10.1038/270725a0 · Cited by 2,153 · see citing works
Marine omega-3 fatty acids and inflammatory processes: effects, mechanisms and clinical relevance
Calder, P. C. (2015) · Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids · doi:10.1016/j.bbalip.2014.08.010 · Cited by 1,717 · see citing works
Protein degradation by the ubiquitin-proteasome pathway in normal and disease states
Lecker, S. H., Goldberg, A. L., & Mitch, W. E. (2006) · Journal of the American Society of Nephrology · doi:10.1681/asn.2006010083 · Cited by 1,234 · see citing works
Sandri, M., Lin, J., Handschin, C., Yang, W., Arany, Z. P., Lecker, S. H., Goldberg, A. L., & Spiegelman, B. M. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0607795103 · Cited by 974 · see citing works
Conversion of <b>α</b> -linolenic acid to longer-chain polyunsaturated fatty acids in human adults
Burdge, G. C., & Calder, P. C. (2005) · Reproduction Nutrition Development · doi:10.1051/rnd:2005047 · Cited by 939 · see citing works
Cornelison, D., & Wold, B. J. (1997) · Developmental Biology · doi:10.1006/dbio.1997.8721 · Cited by 934 · see citing works
Mechanisms of Action of (n-3) Fatty Acids,
Calder, P. C. (2012) · Journal of Nutrition · doi:10.3945/jn.111.155259 · Cited by 871 · see citing works
Plasticity of the Differentiated State
Blau, H. M., Pavlath, G. K., Hardeman, E. C., Chiu, C., Silberstein, L., Webster, S. G., Miller, S. C., & Webster, C. (1985) · Science · doi:10.1126/science.2414846 · Cited by 840 · see citing works
Satellite Cells and Skeletal Muscle Regeneration
Dumont, N. A., Bentzinger, C. F., Sincennes, M., & Rudnicki, M. A. (2015) · Comprehensive Physiology · doi:10.1002/cphy.c140068 · Cited by 719 · see citing works
Smith, G. I., Atherton, P., Reeds, D. N., Mohammed, B. S., Rankin, D., Rennie, M. J., & Mittendorfer, B. (2011) · The American Journal of Clinical Nutrition · doi:10.3945/ajcn.110.005611 · Cited by 665 · see citing works
Pax7 is critical for the normal function of satellite cells in adult skeletal muscle
von Maltzahn, J., Jones, A. E., Parks, R. J., & Rudnicki, M. A. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1307680110 · Cited by 602 · see citing works
Sacheck, J. M., Hyatt, J. K., Raffaello, A., Thomas Jagoe, R., Roy, R. R., Reggie Edgerton, V., Lecker, S. H., & Goldberg, A. L. (2007) · The FASEB Journal · doi:10.1096/fj.06-6604com · Cited by 585 · 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
Dietary fats and membrane function: implications for metabolism and disease
Hulbert, A. J., Turner, N. A., Storlien, L. H., & Else, P. L. (2005) · Biological reviews/Biological reviews of the Cambridge Philosophical Society · doi:10.1017/s1464793104006578 · Cited by 406 · see citing works
Cornelison, D., Filla, M. S., Stanley, H. M., Rapraeger, A. C., & Olwin, B. B. (2001) · Developmental Biology · doi:10.1006/dbio.2001.0416 · Cited by 399 · see citing works
Cardioprotective mechanism of omega-3 polyunsaturated fatty acids
Endo, J., & Arita, M. (2016) · Journal of Cardiology · doi:10.1016/j.jjcc.2015.08.002 · Cited by 369 · see citing works
Burattini, S., Ferri, P., Battistelli, M., Curci, R., Luchetti, F., & Falcieri, E. (2004) · PubMed · doi:10.4081/891 · Cited by 353 · see citing works
Handschin, C., Choi, C. S., Chin, S., Kim, S., Kawamori, D., Kurpad, A. J., Neubauer, N., Hu, J., Mootha, V. K., Kim, Y.-B., et al. (2007) · Journal of Clinical Investigation · doi:10.1172/jci31785 · Cited by 335 · see citing works
Functional and Metabolic Consequences of Sarcopenia
Vandervoort, A. A., & Symons, T. B. (2001) · Canadian Journal of Applied Physiology · doi:10.1139/h01-007 · Cited by 324 · see citing works
Visser, M., & Schaap, L. A. (2011) · Clinics in Geriatric Medicine · doi:10.1016/j.cger.2011.03.006 · Cited by 320 · see citing works
Olsen, S., Aagaard, P., Kadi, F., Tufekovic, G., Verney, J., Olesen, J. L., Suetta, C., & Kjær, M. (2006) · The Journal of Physiology · doi:10.1113/jphysiol.2006.107359 · Cited by 319 · 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
Cornelison, D. D. W., Wilcox-Adelman, S. A., Goetinck, P. F., Rauvala, H., Rapraeger, A. C., & Olwin, B. B. (2004) · Genes & Development · doi:10.1101/gad.1214204 · Cited by 317 · see citing works
Olguín, H. C., Yang, Z., Tapscott, S. J., & Olwin, B. B. (2007) · The Journal of Cell Biology · doi:10.1083/jcb.200608122 · Cited by 311 · see citing works
Wilson, G. J., Wilson, J. M., & Manninen, A. H. (2008) · Nutrition & Metabolism · doi:10.1186/1743-7075-5-1 · Cited by 306 · see citing works
Robinson, S. M., Jameson, K. A., Batelaan, S. F., Martin, H. J., Syddall, H. E., Dennison, E. M., Cooper, C., Sayer, A. A., & the Hertfordshire Cohort Study Group (2008) · Journal of the American Geriatrics Society · doi:10.1111/j.1532-5415.2007.01478.x · Cited by 282 · see citing works
The muscle-specific ubiquitin ligase atrogin-1/MAFbx mediates statin-induced muscle toxicity
Hanai, J., Cao, P., Tanksale, P., Imamura, S., Koshimizu, E., Zhao, J., Kishi, S., Yamashita, M., Phillips, P. S., Sukhatme, V. P., et al. (2007) · Journal of Clinical Investigation · doi:10.1172/jci32741 · Cited by 281 · see citing works
Dietary fat: exogenous determination of membrane structure and cell function
Clandinin, M. T., Cheema, S. K., Field, C. J., et al. (1991) · The FASEB Journal · doi:10.1096/fasebj.5.13.1916101 · Cited by 272 · see citing works
A plea to reduce or replace fetal bovine serum in cell culture media
Gstraunthaler, G. J. A., Lindl, T., & van der Valk, J. (2013) · Cytotechnology · doi:10.1007/s10616-013-9633-8 · Cited by 265 · see citing works
Effect of denervation on mitochondrially mediated apoptosis in skeletal muscle.
Adhihetty, P. J., O'Leary, M. F. N., Chabi, B., Wicks, K. L., & Hood, D. A. (2007) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00768.2006 · Cited by 240 · see citing works
Impaired PGC-1α function in muscle in Huntington's disease
Chaturvedi, R. K., Adhihetty, P. J., Shukla, S., Hennessy, T., Calingasan, N. Y., Yang, L., Starkov, A. A., Kiaei, M., Cannella, M., Sassone, J., et al. (2009) · Human Molecular Genetics · doi:10.1093/hmg/ddp243 · Cited by 237 · see citing works
Therapeutic potential of n-3 polyunsaturated fatty acids in disease
Fetterman, J. W., & Zdanowicz, M. M. (2009) · American Journal of Health-System Pharmacy · doi:10.2146/ajhp080411 · Cited by 236 · see citing works
Functional and Metabolic Consequences of Sarcopenia
Evans, W. J. (1997) · Journal of Nutrition · doi:10.1093/jn/127.5.998s · Cited by 220 · see citing works
Field, C. J., Ryan, E. A., Thomson, A. B. R., & Clandinin, M. T. (1990) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(19)38569-2 · Cited by 215 · see citing works
Delarue, J., Foll, C. L., Corporeau, C., & Lucas, D. (2004) · annales de biologie animale biochimie biophysique · doi:10.1051/rnd:2004033 · Cited by 203 · see citing works
Wigmore, S. J., Fearon, K. C. H., Maingay, J. P., & Ross, J. A. (1997) · Clinical Science · doi:10.1042/cs0920215 · Cited by 195 · see citing works
Seale, P., Ishibashi, J., Scimè, A., & Rudnicki, M. A. (2004) · PLoS Biology · doi:10.1371/journal.pbio.0020130 · Cited by 186 · see citing works
Langelaan, M. L. P., Boonen, K. J. M., Rosaria-Chak, K. Y., van der Schaft, D. W. J., Post, M. J., & Baaijens, F. F. (2010) · Journal of Tissue Engineering and Regenerative Medicine · doi:10.1002/term.345 · Cited by 175 · see citing works
Regulation of Satellite Cell Function in Sarcopenia
Alway, S. E., Myers, M. J., & Mohamed, J. S. (2014) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2014.00246 · Cited by 160 · see citing works
Tumor necrosis factor-α inhibits myogenesis through redox-dependent and -independent pathways
LANGEN, R. C. J., Schols, A. M. W. J., KELDERS, M. C. J. M., van der Velden, J. L. J., Wouters, E. F. �., & Janssen-Heininger, Y. M. W. (2002) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00418.2001 · Cited by 132 · see citing works
Involvement of myogenic regulator factors during fusion in the cell line C2C12
Dedieu, S., Mazères, G., Cottin, P., & Brustis, J. (2002) · The International Journal of Developmental Biology · doi:10.1387/ijdb.11934152 · Cited by 129 · see citing works
Gutiérrez, J., & Brandan, E. (2010) · Molecular and Cellular Biology · doi:10.1128/mcb.01164-09 · Cited by 122 · see citing works
Effect of diet on activity of enzymes involved in fatty acid and cholesterol synthesis.
Romsos, D. R., & Leveille, G. A. (1974) · PubMed · Cited by 118 · see citing works
Yang, M. J., Wei, D., Mo, C., Zhang, J., Wang, X., Han, X., Wang, Z., & Xiao, H. (2013) · Lipids in Health and Disease · doi:10.1186/1476-511x-12-104 · Cited by 116 · see citing works
Alway, S. E., Pereira, S. L., Edens, N. K., Hao, Y., & Bennett, B. T. (2013) · Experimental Gerontology · doi:10.1016/j.exger.2013.06.005 · Cited by 114 · see citing works
Vaughan, R. A., Garcia-Smith, R., Bisoffi, M., Conn, C. A., & Trujillo, K. A. (2012) · Lipids in Health and Disease · doi:10.1186/1476-511x-11-142 · Cited by 112 · 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
Eicosapentaenoic acid in cancer improves body composition and modulates metabolism
Pappalardo, G., Almeida, A. G., & Ravasco, P. (2014) · Nutrition · doi:10.1016/j.nut.2014.12.002 · Cited by 102 · see citing works
Romsos, D. R., & Leveille, G. A. (1974) · Advances in lipid research · doi:10.1016/b978-0-12-024912-1.50010-7 · Cited by 97 · see citing works
Changes in serum influence the fatty acid composition of established cell lines
Stoll, L. L., & Spector, A. A. (1984) · In Vitro Cellular & Developmental Biology - Plant · doi:10.1007/bf02618879 · Cited by 96 · see citing works
Murphy, R. A., Mourtzakis, M., Chu, Q. S.-C., Reiman, T., & Mazurak, V. C. (2010) · Journal of Nutrition · doi:10.3945/jn.110.123521 · Cited by 94 · see citing works
Self-citationRegulation of muscle protein synthesis in humans
Phillips, B. E., Hill, D. S., & Atherton, P. J. (2012) · Current Opinion in Clinical Nutrition and Metabolic Care · doi:10.1097/mco.0b013e32834d19bc · Cited by 91 · see citing works
Dollenmeier, P., Turner, D. C., & Eppenberger, H. M. (1981) · Experimental Cell Research · doi:10.1016/0014-4827(81)90298-6 · Cited by 89 · see citing works
Penna, F., Busquets, S., Pin, F., Toledo, M., Baccino, F. M., López-Soriano, F. J., Costelli, P., & Argilés, J. M. A. (2011) · Journal of Cachexia Sarcopenia and Muscle · doi:10.1007/s13539-011-0028-4 · Cited by 86 · see citing works
Inhibition of myogenic differentiation in myoblasts expressing a truncated type II TGF-β receptor
Filvaroff, E. H., Ebner, R., & Derynck, R. (1994) · Development · doi:10.1242/dev.120.5.1085 · Cited by 84 · see citing works
Can muscle regeneration fail in chronic inflammation: a weakness in inflammatory myopathies?
Loell, I., & Lundberg, I. E. (2011) · Journal of Internal Medicine · doi:10.1111/j.1365-2796.2010.02334.x · Cited by 82 · see citing works
Age-Related Changes in Speed and Mechanism of Adult Skeletal Muscle Stem Cell Migration
Collins‐Hooper, H., Woolley, T. E., Dyson, L., Patel, A. P., Potter, P. K., Baker, R. E., Gaffney, E. A., Maini, P. K., Dash, P. R., & Patel, K. (2012) · Stem Cells · doi:10.1002/stem.1088 · Cited by 82 · see citing works
Plasma Polyunsaturated Fatty Acids and Age-Related Physical Performance Decline
Abbatecola, A. M., Cherubini, A., Guralnik, J. M., Andrés‐Lacueva, C., Ruggiero, C., Maggio, M. G., Bandinelli, S., Paolisso, G., & Ferrucci, L. (2009) · Rejuvenation Research · doi:10.1089/rej.2008.0799 · Cited by 82 · see citing works
n-3 polyunsaturated fatty acids
Murphy, R. A., Mourtzakis, M., & Mazurak, V. C. (2012) · Current Opinion in Clinical Nutrition & Metabolic Care · doi:10.1097/mco.0b013e328351c32f · Cited by 78 · see citing works
Self-citationFarup, 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
Glucocorticoid effects on insulin- and IGF-I-regulated muscle protein metabolism during aging
Dardevet, D. P., Sornet, C., Savary‐Auzeloux, I., Debras, E., Patureau-Mirand, P., & Grizard, J. (1998) · Journal of Endocrinology · doi:10.1677/joe.0.1560083 · Cited by 75 · see citing works
Smith, H. J., Greenberg, N. A., & Tisdale, M. J. (2004) · British Journal of Cancer · doi:10.1038/sj.bjc.6601981 · Cited by 74 · see citing works
Diel, P. R., Baadners, D., Schlüpmann, K., Velders, M., & Schwarz, J. P. (2008) · Journal of Molecular Endocrinology · doi:10.1677/jme-07-0175 · Cited by 74 · see citing works
Alway, S. E., Bennett, B. T., Wilson, J. C., Sperringer, J., Mohamed, J. S., Edens, N. K., & Pereira, S. L. (2015) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00674.2014 · Cited by 73 · see citing works
Layne, M. D., & Farmer, S. R. (1999) · Experimental Cell Research · doi:10.1006/excr.1999.4465 · Cited by 71 · see citing works
Farup, J., Rahbek, S. K., Riis, S., Vendelbo, M. H., Paoli, F. D., & Vissing, K. (2014) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00261.2014 · Cited by 70 · see citing works
Johnson, M. L., Lalia, A. Z., Dasari, S., Pallauf, M., Fitch, M., Hellerstein, M. K., & Lanza, I. R. (2015) · Aging Cell · doi:10.1111/acel.12352 · Cited by 66 · see citing works
Docosahexaenoic Acid Protects Muscle Cells from Palmitate-Induced Atrophy
Bryner, R. W., Woodworth‐Hobbs, M. E., Williamson, D. L., & Alway, S. E. (2012) · ISRN Obesity · doi:10.5402/2012/647348 · Cited by 66 · see citing works
Magee, P., Pearson, S., Whittingham-Dowd, J., & Allen, J. (2012) · The Journal of Nutritional Biochemistry · doi:10.1016/j.jnutbio.2011.09.005 · Cited by 65 · see citing works
Velleman, S. G., Nestor, K., Coy, C. S., Harford, I., & ANTHONY, N. B. (2010) · International Journal of Poultry Science · doi:10.3923/ijps.2010.417.425 · Cited by 63 · see citing works
Why do we still use serum in the production of biopharmaceuticals?
Shah, G. (1999) · PubMed · Cited by 60 · see citing works
Epigallocatechin-3-gallate improves plantaris muscle recovery after disuse in aged rats
Alway, S. E., Bennett, B., Wilson, J. C., Edens, N. K., & Pereira, S. L. (2013) · Experimental Gerontology · doi:10.1016/j.exger.2013.11.011 · Cited by 60 · see citing works
Role of n-3 fatty acids in muscle loss and myosteatosis
Ewaschuk, J. B., Al-Masud, A. A., & Mazurak, V. C. (2014) · Applied Physiology, Nutrition, and Metabolism · doi:10.1139/apnm-2013-0423 · Cited by 55 · see citing works
Self-citationTolosa, L., Morlá, M., Iglesias, A., Busquets, X., Lladó, J., & Olmos, G. (2005) · Cellular Signalling · doi:10.1016/j.cellsig.2005.02.001 · Cited by 53 · see citing works
Functional crosstalk of PGC-1 coactivators and inflammation in skeletal muscle pathophysiology
Eisele, P. S., & Handschin, C. (2013) · Seminars in Immunopathology · doi:10.1007/s00281-013-0406-4 · Cited by 53 · see citing works
Castillero, E., Martín, A. I., López-Menduiña, M., Villanúa, M. A., & López-Calderón, A. (2009) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00388.2009 · Cited by 53 · see citing works
Kotliar, N., & Pilch, P. F. (1992) · Molecular Endocrinology · doi:10.1210/mend.6.3.1584210 · Cited by 52 · see citing works
Dangardt, F., Chen, Y., Gronowitz, E., Dahlgren, J., Friberg, P., & Strandvik, B. (2012) · Journal of Nutrition and Metabolism · doi:10.1155/2012/395757 · Cited by 52 · see citing works
Slee, E. L., McLennan, P. L., Owen, A. J., & Theiss, M. L. (2010) · Journal of Lipid Research · doi:10.1194/jlr.m004069 · Cited by 43 · see citing works
Different effects of omega-3 fatty acids on the cell cycle in c2c12 myoblast proliferation
Peng, Y., Zheng, Y., Zhang, Y., Zhao, J., Chang, F., Lu, T., Zhang, R., Li, Q., Hu, X., & Li, N. (2012) · Molecular and Cellular Biochemistry · doi:10.1007/s11010-012-1329-4 · Cited by 34 · see citing works
The effect of nutritional status on myogenic satellite cell proliferation and differentiation
Powell, D. J., McFarland, D. C., Cowieson, A. J., et al. (2013) · Poultry Science · doi:10.3382/ps.2013-03107 · Cited by 33 · see citing works
An Omega-3 Fatty Acid-Enriched Diet Prevents Skeletal Muscle Lesions in a Hamster Model of Dystrophy
Fiaccavento, R., Carotenuto, F., Vecchini, A., Binaglia, L., Forte, G., Capucci, E., Maccari, A. M., Minieri, M., & Nardo, P. D. (2010) · American Journal Of Pathology · doi:10.2353/ajpath.2010.100174 · Cited by 32 · see citing works
Librán-Pérez, M., Figueiredo-Silva, A. C., Panserat, S., Geurden, I., Míguez, J. M., Polakof, S., & Soengas, J. L. (2012) · Comparative Biochemistry and Physiology Part A Molecular & Integrative Physiology · doi:10.1016/j.cbpa.2012.09.012 · Cited by 29 · see citing works
The Effects of Omega-3 Fatty Acid Supplementation on Dexamethasone-Induced Muscle Atrophy
Fappi, A., Godoy, T. S., Maximino, J. R., Rizzato, V. R., Neves, J. D. C., Chadi, G., & Zanoteli, E. (2014) · BioMed Research International · doi:10.1155/2014/961438 · Cited by 29 · see citing works
Diet composition as a source of variation in experimental animal models of cancer cachexia
Giles, K. H., Chen, G., Jagoe, R. T., et al. (2015) · Journal of Cachexia Sarcopenia and Muscle · doi:10.1002/jcsm.12058 · Cited by 28 · see citing works
Shin, J., McFarland, D. C., & Velleman, S. G. (2011) · Poultry Science · doi:10.3382/ps.2011-01695 · Cited by 27 · see citing works
Apolinário, L. M., De Carvalho, S. C., Santo Neto, H., & Marques, M. J. (2015) · The Anatomical Record · doi:10.1002/ar.23177 · Cited by 22 · see citing works
Hashimoto, Y., Yamada, K., Tsushima, H., Miyazawa, D., Mori, M., Nishio, K., Ohkubo, T., Hibino, H., Ohara, N., & Okuyama, H. (2013) · Lipids · doi:10.1007/s11745-013-3805-3 · Cited by 22 · see citing works
PGC-1α is associated with C2C12 Myoblast differentiation
Lin, Y., Zhao, Y., Li, R., Gong, J., Zheng, Y., & Wang, Y. (2014) · Open Life Sciences · doi:10.2478/s11535-014-0341-y · Cited by 22 · see citing works
McFarland, D. C., Velleman, S. G., Pesall, J. E., et al. (2011) · Comparative Biochemistry and Physiology Part A Molecular & Integrative Physiology · doi:10.1016/j.cbpa.2011.02.017 · Cited by 5 · see citing works
Flagged first, then by citations
Cited by
Sorted by citations
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
- Authors
- Bhullar, A. S., Putman, C. T., & Mazurak, V. C.
- Affiliations
- University of Alberta (CA)
- Corresponding author
- Mazurak, Vera C.
- ORCID
- Mazurak, Vera C.
- Venue
- Nutrition and Metabolic Insights
- Publisher
- SAGE Publications
- Published
- 2016-01
- Volume
- 9
- Pages
- 1-10
- ISSN
- 1178-6388 (ISSN-L)
- PMC
- PMC4747635
- OpenAlex
- W2254897605
- Cited by
- 26
- References
- 95
- Citations by year
- 2026: 1 · 2025: 3 · 2024: 6 · 2023: 1 · 2022: 2 · 2021: 2 · 2020: 5 · 2019: 1 · 2018: 2 · 2017: 2 · 2016: 1
- FWCI
- 0.18
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Locations
- Nutrition and Metabolic Insights (publishedVersion, cc-by-nc)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Muscle Physiology and Disorders
- Health Sciences › Nursing › Nutrition and Dietetics › Fatty Acid Research and Health
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Muscle metabolism and nutrition
- Keywords
- omega-3 fatty acids, satellite cells, myogenesis, skeletal muscle regeneration, muscle atrophy, alpha-linolenic acid, eicosapentaenoic acid, docosahexaenoic acid, Pax7, MyoD, myogenin, stem cell proliferation, aging
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