Nrf2 mediates redox adaptations to exercise
Open accessAbstract
The primary aim of this review is to summarize the current literature on the effects of acute exercise and regular exercise on nuclear factor erythroid 2-related factor 2 (Nrf2) activity and downstream targets of Nrf2 signaling. Nrf2 (encoded in humans by the NFE2L2 gene) is the master regulator of antioxidant defenses, a transcription factor that regulates expression of more than 200 cytoprotective genes. Increasing evidence indicates that Nrf2 signaling plays a key role in how oxidative stress mediates the beneficial effects of exercise. Episodic increases in oxidative stress induced through bouts of acute exercise stimulate Nrf2 activation and when applied repeatedly, as with regular exercise, leads to upregulation of endogenous antioxidant defenses and overall greater ability to counteract the damaging effects of oxidative stress. The evidence of Nrf2 activation in response to exercise across variety of tissues may be an important mechanism of how exercise exerts its well-known systemic effects that are not limited to skeletal muscle and myocardium. Additionally there are emerging data that results from animal studies translate to humans.
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Exercise induces Nfe2l2 gene expression, whereas ROS generated during exercise would be expected to increase NFE2L2 stability.
“Exercise induces Nfe2l2 gene expression (7), whereas ROS generated during exercise would be expected to increase NFE2L2 stability (4, 30).”
From Skeletal muscle NOX4 is required for adaptive responses that prevent insulin resistance (2021) · cites this paper as [30]
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1 retracted
Niture, S. K., Jain, A. K., & Jaiswal, A. K. (2009) · Journal of Cell Science · doi:10.1242/jcs.058537 · Cited by 192 · see citing works
RetractedFree radicals and antioxidants in normal physiological functions and human disease
Valko, M., Leibfritz, D., Moncol, J., Cronin, M. T. D., Mazur, M., & Telser, J. (2007) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2006.07.001 · Cited by 14,269 · see citing works
Oxidants, oxidative stress and the biology of ageing
Finkel, T., & Holbrook, N. J. (2000) · Nature · doi:10.1038/35041687 · Cited by 9,413 · see citing works
Glutamate neurotoxicity and diseases of the nervous system
Choi, D. W. (1988) · Neuron · doi:10.1016/0896-6273(88)90162-6 · Cited by 8,152 · see citing works
Cell Survival Responses to Environmental Stresses Via the Keap1-Nrf2-ARE Pathway
Kensler, T. W., Wakabayashi, N., & Biswal, S. (2007) · Annual Review of Pharmacology and Toxicology · doi:10.1146/annurev.pharmtox.46.120604.141046 · Cited by 3,630 · see citing works
Kobayashi, A., Kang, M.-I., Okawa, H., Ohtsuji, M., Zenke, Y., Chiba, T., Igarashi, K., & Yamamoto, M. (2004) · Molecular and Cellular Biology · doi:10.1128/mcb.24.16.7130-7139.2004 · Cited by 2,224 · see citing works
Nrf2:INrf2 (Keap1) signaling in oxidative stress
Kaspar, J. W., Niture, S. K., & Jaiswal, A. K. (2009) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2009.07.035 · Cited by 1,646 · see citing works
Antioxidants prevent health-promoting effects of physical exercise in humans
Ristow, M., Zarse, K., Oberbach, A., Klöting, N., Birringer, M., Kiehntopf, M., Stumvoll, M., Kahn, C. R., & Blüher, M. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0903485106 · Cited by 1,582 · see citing works
Oxidative stress and gene regulation
Allen, R. G., & Tresini, M. (2000) · Free Radical Biology and Medicine · doi:10.1016/s0891-5849(99)00242-7 · Cited by 1,297 · see citing works
Regulatory Mechanisms Controlling Gene Expression Mediated by the Antioxidant Response Element
Nguyen, T., Sherratt, P. J., & Pickett, C. B. (2003) · The Annual Review of Pharmacology and Toxicology · doi:10.1146/annurev.pharmtox.43.100901.140229 · Cited by 1,232 · see citing works
Moderate exercise is an antioxidant: Upregulation of antioxidant genes by training
Gomez-Cabrera, M.-C., Domenech, E., & Viña, J. (2008) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2007.02.001 · Cited by 1,020 · see citing works
Kobayashi, A., Kang, M.-I., Watai, Y., Tong, K. I., Shibata, T., Uchida, K., & Yamamoto, M. P. (2005) · Molecular and Cellular Biology · doi:10.1128/mcb.26.1.221-229.2006 · Cited by 933 · see citing works
Kobayashi, M., & Yamamoto, M. P. (2006) · Advances in Enzyme Regulation · doi:10.1016/j.advenzreg.2006.01.007 · Cited by 855 · see citing works
Gomez-Cabrera, M.-C., Domenech, E., Romagnoli, M., Arduini, A., Borras, C., Pallardo, F. V., Sastre, J., & Viña, J. (2008) · The American Journal of Clinical Nutrition · doi:10.1093/ajcn/87.1.142 · Cited by 844 · see citing works
Nrf2 enhances resistance of cancer cells to chemotherapeutic drugs, the dark side of Nrf2
Wang, X.-J., Sun, Z., Villeneuve, N. F., Zhang, S., Zhao, F., Li, Y., Chen, W., Yi, X., Zheng, W., Wondrak, G. T., et al. (2008) · Carcinogenesis · doi:10.1093/carcin/bgn095 · Cited by 839 · see citing works
Tebay, L. E., Robertson, H., Durant, S. T., Vitale, S. R., Penning, T. M., Dinkova-Kostova, A. T., & Hayes, J. D. (2015) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2015.06.021 · Cited by 837 · see citing works
The Molecular Bases of Training Adaptation
Coffey, V. G., & Hawley, J. A. (2007) · Sports Medicine · doi:10.2165/00007256-200737090-00001 · Cited by 756 · see citing works
Kobayashi, M., Li, L., Iwamoto, N., Nakajima‐Takagi, Y., Kaneko, H., Nakayama, Y., Eguchi, M., Wada, Y., Kumagai, Y., & Yamamoto, M. P. (2008) · Molecular and Cellular Biology · doi:10.1128/mcb.01080-08 · Cited by 641 · see citing works
Perry, C. G. R., Lally, J., Holloway, G. P., Heigenhauser, G. J. F., Bonen, A., & Spriet, L. L. (2010) · The Journal of Physiology · doi:10.1113/jphysiol.2010.199448 · Cited by 559 · see citing works
Nrf2: friend or foe for chemoprevention?
Kensler, T. W., & Wakabayashi, N. (2009) · Carcinogenesis · doi:10.1093/carcin/bgp231 · Cited by 487 · see citing works
Antioxidants and oxidants regulated signal transduction pathways
Owuor, E. D., & Kong, A. T. (2002) · Biochemical Pharmacology · doi:10.1016/s0006-2952(02)01137-1 · Cited by 439 · see citing works
Role of Polyphenols and Other Phytochemicals on Molecular Signaling
Upadhyay, S., & Dixit, M. (2015) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2015/504253 · Cited by 382 · see citing works
Hormetic Dietary Phytochemicals
Son, T. G., Camandola, S., & Mattson, M. P. (2008) · NeuroMolecular Medicine · doi:10.1007/s12017-008-8037-y · Cited by 362 · see citing works
Identification of the interactive interface and phylogenic conservation of the Nrf2‐Keap1 system
Kobayashi, M., Itoh, K., Suzuki, T., Osanai, H., Nishikawa, K., Katoh, Y., Takagi, Y., & Yamamoto, M. P. (2002) · Genes to Cells · doi:10.1046/j.1365-2443.2002.00561.x · Cited by 340 · see citing works
Shih, P., Yeh, C., & Yen, G. (2007) · Journal of Agricultural and Food Chemistry · doi:10.1021/jf071933i · Cited by 333 · see citing works
Muthusamy, V. R., Kannan, S., Sadhaasivam, K., Gounder, S. S., Davidson, C. J., Boeheme, C., Hoidal, J. R., Wang, L., & Rajasekaran, N. S. (2011) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2011.10.440 · Cited by 316 · see citing works
Effect of Antioxidants Supplementation on Aging and Longevity
Sadowska‐Bartosz, I., & Bartosz, G. (2014) · BioMed Research International · doi:10.1155/2014/404680 · Cited by 298 · see citing works
Lifelong physical exercise delays age-associated skeletal muscle decline
Zampieri, S., Pietrangelo, L., Loefler, S., Fruhmann, H., Vogelauer, M., Burggraf, S., Pond, A., Grim-Stieger, M., Cvecka, J., Sedliak, M., et al. (2015) · The Journals of Gerontology Series A: Biological Sciences and Medical Sciences · doi:10.1093/gerona/glu006 · Cited by 282 · see citing works
Validation of the multiple sensor mechanism of the Keap1-Nrf2 system
Takaya, K., Suzuki, T., Motohashi, H., Onodera, K., Satomi, S., Kensler, T. W., & Yamamoto, M. P. (2012) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2012.06.023 · Cited by 277 · see citing works
Merry, T. L., & Ristow, M. (2016) · The Journal of Physiology · doi:10.1113/jp271957 · Cited by 246 · see citing works
Antioxidant supplements and mortality
Bjelakovic, G., Nikolova, D., & Gluud, C. (2013) · Current Opinion in Clinical Nutrition and Metabolic Care · doi:10.1097/mco.0000000000000009 · Cited by 234 · see citing works
Antioxidant Supplementation Reduces Skeletal Muscle Mitochondrial Biogenesis
Strobel, N., Peake, J. M., Matsumoto, A., Marsh, S. A., Coombes, J. S., & Wadley, G. D. (2010) · Medicine & Science in Sports & Exercise · doi:10.1249/mss.0b013e318203afa3 · Cited by 187 · see citing works
Fuentes, F., Paredes‐Gonzalez, X., & Kong, A. T. (2015) · Current Pharmacology Reports · doi:10.1007/s40495-015-0017-y · Cited by 185 · see citing works
Mechanism of Chemical Activation of Nrf2
Li, Y., Paonessa, J. D., & Zhang, Y. (2012) · PLoS ONE · doi:10.1371/journal.pone.0035122 · Cited by 179 · see citing works
The Keap1–Nrf2 Cell Defense Pathway – A Promising Therapeutic Target?
Copple, I. M. (2012) · Advances in pharmacology · doi:10.1016/b978-0-12-398339-8.00002-1 · Cited by 172 · see citing works
Gounder, S. S., Kannan, S., Devadoss, D., Miller, C. J., Whitehead, K. S., Odelberg, S. J., Firpo, M. A., Paine, R., Hoidal, J. R., Abel, E. D., et al. (2012) · PLoS ONE · doi:10.1371/journal.pone.0045697 · Cited by 171 · see citing works
Morrison, D., Hughes, J., Della Gatta, P. A., Mason, S., Lamon, S., Russell, A. P., & Wadley, G. D. (2015) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2015.10.412 · Cited by 171 · see citing works
Csiszár, A., Gautam, T., Sosnowska, D., Tarantini, S., Banki, E., Tucsek, Z., Tóth, P., Losonczy, G., Koller, Á., Reglődi, D., et al. (2014) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.00307.2014 · Cited by 161 · see citing works
Dysfunctional Nrf2–Keap1 redox signaling in skeletal muscle of the sedentary old
Safdar, A., DeBeer, J., & Tarnopolsky, M. A. (2010) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2010.08.010 · Cited by 158 · see citing works
The Predicted Molecular Weight of Nrf2: It Is What It Is Not
Lau, A., Tian, W., Whitman, S. A., & Zhang, D. D. (2012) · Antioxidants and Redox Signaling · doi:10.1089/ars.2012.4754 · Cited by 154 · see citing works
Translational Control of Nrf2 Protein in Activation of Antioxidant Response by Oxidants
Purdom, S., Sheveleva, E. V., Sun, H., & Chen, Q. M. (2007) · Molecular Pharmacology · doi:10.1124/mol.107.035360 · Cited by 144 · see citing works
Frugal chemoprevention: targeting Nrf2 with foods rich in sulforaphane
Yang, L., Palliyaguru, D. L., & Kensler, T. W. (2015) · Seminars in Oncology · doi:10.1053/j.seminoncol.2015.09.013 · Cited by 139 · see citing works
Seals, D. R., Kaplon, R. E., Gioscia‐Ryan, R. A., & LaRocca, T. J. (2014) · Physiology · doi:10.1152/physiol.00059.2013 · Cited by 138 · see citing works
NRF2, cancer and calorie restriction
Martín‐Montalvo, A., Villalba, J. M., Navas, P., & de Cabo, R. (2010) · Oncogene · doi:10.1038/onc.2010.492 · Cited by 128 · see citing works
Exercise-induced skeletal muscle signaling pathways and human athletic performance
Camera, D. M., Smiles, W. J., & Hawley, J. A. (2016) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2016.02.007 · Cited by 128 · see citing works
Asghar, M., George, L., & Lokhandwala, M. F. (2007) · American Journal of Physiology-Renal Physiology · doi:10.1152/ajprenal.00272.2007 · Cited by 111 · see citing works
The clinical potential of influencing Nrf2 signaling in degenerative and immunological disorders
Hybertson, B. M., Gao, B., & Doan, A. (2014) · Clinical Pharmacology Advances and Applications · doi:10.2147/cpaa.s35078 · Cited by 110 · see citing works
Cobley, J. N., Sakellariou, G. K., Owens, D. J., Murray, S. W., Waldron, S., Gregson, W. A., Fraser, W. D., Burniston, J. G., Iwanejko, L., McArdle, A., et al. (2014) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2014.02.004 · Cited by 105 · see citing works
Malaguti, M., Angeloni, C., Garatachea, N., Baldini, M., Leoncini, E., Collado, P. S., Teti, G., Falconi, M., Gonzalez-Gallego, J., & Hrelia, S. (2009) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00293.2009 · Cited by 103 · see citing works
Exercise-induced Nrf2-signaling is impaired in aging
Done, A. J., Gage, M. J., Nieto, N. C., & Traustadóttir, T. (2016) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2016.04.024 · Cited by 99 · see citing works
Self-citationWang, P., Li, C. G., Qi, Z., Cui, D., & Ding, S. (2015) · Experimental Physiology · doi:10.1113/ep085493 · Cited by 96 · see citing works
Tsou, Y.-H., Shih, C.-T., Ching, C., Huang, J.-Y., Jen, C. J., Yu, L., Kuo, Y., Wu, F., & Chuang, J. (2014) · Experimental Neurology · doi:10.1016/j.expneurol.2014.09.021 · Cited by 95 · see citing works
Wray, D. W., Uberoi, A., Lawrenson, L., Bailey, D. M., & Richardson, R. S. (2008) · Clinical Science · doi:10.1042/cs20080337 · Cited by 93 · see citing works
Translational Geroscience: Emphasizing function to achieve optimal longevity
Seals, D. R., & Melov, S. (2014) · Aging · doi:10.18632/aging.100694 · Cited by 90 · see citing works
Nrf2 deficiency promotes apoptosis and impairs PAX7/MyoD expression in aging skeletal muscle cells
Narasimhan, M., Hong, J., Atieno, N., Muthusamy, V. R., Davidson, C. J., Abu-Rmaileh, N., Richardson, R. S., Gomes, A. V., Hoidal, J. R., & Rajasekaran, N. S. (2014) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2014.02.023 · Cited by 87 · see citing works
Aging of signal transduction pathways, and pathology
Carlson, M. E., Silva, H. S., & Conboy, I. M. (2008) · Experimental Cell Research · doi:10.1016/j.yexcr.2008.03.017 · Cited by 83 · see citing works
Xue, M., Momiji, H., Rabbani, N., Barker, G. C., Bretschneider, T., Shmygol, A., Rand, D. A. J., & Thornalley, P. J. (2014) · Antioxidants and Redox Signaling · doi:10.1089/ars.2014.5962 · Cited by 83 · see citing works
Aguiar, A. S., Duzzioni, M., Remor, A. P., Tristão, F. S. M., MATHEUS, F. C., Raisman‐Vozari, R., Latini, A., & Prediger, R. D. (2015) · Neurochemical Research · doi:10.1007/s11064-015-1709-8 · Cited by 82 · see citing works
Lamprecht, M., Greilberger, J., Schwaberger, G., Hofmann, P., & Oettl, K. (2008) · Journal of Applied Physiology · doi:10.1152/japplphysiol.01325.2007 · Cited by 75 · see citing works
Kumar, R., Negi, P. S., Singh, B., Ilavazhagan, G., Bhargava, K., & Sethy, N. K. (2011) · Journal of Ethnopharmacology · doi:10.1016/j.jep.2011.04.040 · Cited by 73 · see citing works
Roles of Keap1–Nrf2 System in Upper Aerodigestive Tract Carcinogenesis
Ohkoshi, A., Suzuki, T., Ono, M., Kobayashi, T., & Yamamoto, M. P. (2012) · Cancer Prevention Research · doi:10.1158/1940-6207.capr-12-0401-t · Cited by 69 · see citing works
NRF2 and the Phase II Response in Acute Stress Resistance Induced by Dietary Restriction
Hine, C. (2012) · Journal of Clinical & Experimental Pathology · doi:10.4172/2161-0681.s4-004 · Cited by 68 · see citing works
Li, T., He, S., Liu, S., Kong, Z., Wang, J., & Zhang, Y. (2015) · Free Radical Research · doi:10.3109/10715762.2015.1066784 · Cited by 67 · see citing works
Ginsenoside Rg3 improves cardiac mitochondrial population quality: Mimetic exercise training
Sun, M., Huang, C., Wang, C., Zheng, J., Zhang, P., Xu, Y., Chen, H., & Shen, W. (2013) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2013.10.039 · Cited by 66 · see citing works
Zhao, X., Bian, Y., Sun, Y., Li, L., Wang, L., Chunfang, Z., Shen, Y., Song, Q., Qu, Y., Niu, S., et al. (2013) · Experimental Gerontology · doi:10.1016/j.exger.2013.05.063 · Cited by 60 · see citing works
George, L. E., Lokhandwala, M. F., & Asghar, M. (2009) · American Journal of Physiology-Renal Physiology · doi:10.1152/ajprenal.00397.2009 · Cited by 58 · see citing works
Hu, L., Miao, W., Loignon, M., Kandouz, M., & Batist, G. (2009) · Cancer Chemotherapy and Pharmacology · doi:10.1007/s00280-009-1182-7 · Cited by 53 · see citing works
Nuclear factor-erythroid 2-related factor 2 as a chemopreventive target in colorectal cancer
Saw, C. L. L., & Kong, A. T. (2011) · Expert Opinion on Therapeutic Targets · doi:10.1517/14728222.2011.553602 · Cited by 51 · see citing works
Cytoprotective Role of Nrf2 in Electrical Pulse Stimulated C2C12 Myotube
Horie, M., Warabi, E., Komine, S., Oh, S., & Shoda, J. (2015) · PLoS ONE · doi:10.1371/journal.pone.0144835 · Cited by 48 · see citing works
Coenzyme Q10 Supplementation Modulates NFκB and Nrf2 Pathways in Exercise Training.
Pala, R., Orhan, C., Tuzcu, M., Şahin, N., Ali, S., Çınar, V., Atalay, M., & Şahin, K. (2016) · PubMed Central · Cited by 47 · see citing works
Scott, H. A., Latham, J. R., Callister, R., Pretto, J. J., Baines, K. J., Saltos, N., Upham, J. W., & Wood, L. G. (2015) · Annals of Allergy Asthma & Immunology · doi:10.1016/j.anai.2015.04.002 · Cited by 46 · see citing works
Fiorin, F. D. S., Ferreira, A. P. D. O., Ribeiro, L. R., Silva, L. F. A., de Castro, M. R. T., da Silva, L. R. H., da Silveira, M. E. P., Zemolin, A. P. P., Dobrachinski, F., Oliveira, S. M., et al. (2015) · Journal of Neurotrauma · doi:10.1089/neu.2015.4068 · Cited by 44 · see citing works
Exercise-induced oxidative stress and hypoxic exercise recovery
Ballmann, C. G., McGinnis, G. R., Peters, B. A., et al. (2014) · European Journal of Applied Physiology · doi:10.1007/s00421-013-2806-5 · Cited by 43 · see citing works
Shenvi, S. V., Smith, E. J. T., & Hagen, T. M. (2011) · Aging Cell · doi:10.1111/j.1474-9726.2011.00788.x · Cited by 43 · see citing works
Comparison of human Nrf2 antibodies: A tale of two proteins
Kemmerer, Z. A., Ader, N. R., Mulroy, S. S., & Eggler, A. L. (2015) · Toxicology Letters · doi:10.1016/j.toxlet.2015.07.004 · Cited by 41 · see citing works
Singh, M., Tulsawani, R., Koganti, P., et al. (2013) · BioMed Research International · doi:10.1155/2013/569206 · Cited by 41 · see citing works
Jiang, H., Miao, Y., Wang, Y., Zhao, M., Feng, Z., Yu, X., Liu, J., & Zang, W. (2014) · Clinical and Experimental Pharmacology and Physiology · doi:10.1111/1440-1681.12211 · Cited by 40 · see citing works
Tang, F., Lü, M., Zhang, S., et al. (2014) · Lipids · doi:10.1007/s11745-014-3962-z · Cited by 39 · see citing works
Michele Salanova, A., Schiffl, G., Gutsmann, M., Felsenberg, D., Furlan, S., Pompeo Volpe, D., Clarke, A. H., & Blottner, D. (2013) · Redox Biology · doi:10.1016/j.redox.2013.10.006 · Cited by 33 · see citing works
Camiletti‐Moirón, D., Aparicio, V. A., Nebot, E., Medina, G. E., Martínez, R., Kapravelou, G., Andrade, A., Porres, J. M., López-Jurado, M., & Aranda, P. (2014) · PubMed · doi:10.3305/nh.2015.31.2.8182 · Cited by 32 · see citing works
Bos, I., Boever, P. D., Panis, L. I., Sarre, S., & MEEUSEN, R. R. (2012) · Neuroscience · doi:10.1016/j.neuroscience.2012.07.057 · Cited by 29 · see citing works
Gomes, F. C., Chuffa, L. G. D. A., Scarano, W. R., et al. (2016) · Andrology · doi:10.1111/andr.12162 · Cited by 19 · see citing works
Takahashi, S., Izawa, Y., & Suzuki, N. (2012) · Rinsho Shinkeigaku · doi:10.5692/clinicalneurol.52.41 · Cited by 19 · see citing works
High-intensity Exercise Modifies the Effects of Stanozolol on Brain Oxidative Stress in Rats
Camiletti‐Moirón, D., Aparicio, V. A., Nebot, E., et al. (2015) · International Journal of Sports Medicine · doi:10.1055/s-0035-1548941 · Cited by 17 · see citing works
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- Authors
- Done, A. J., & Traustadóttir, T.
- Affiliations
- Northern Arizona University (US)
- Corresponding author
- Traustadóttir, Tinna
- Venue
- Redox Biology
- Publisher
- Elsevier BV
- Published
- 2016-12
- Volume
- 10
- Pages
- 191-199
- ISSN
- 2213-2317 (ISSN-L)
- PMC
- PMC5078682
- OpenAlex
- W2532167704
- Cited by
- 308
- References
- 84
- Citations by year
- 2026: 45 · 2025: 27 · 2024: 33 · 2023: 29 · 2022: 32 · 2021: 52 · 2020: 34 · 2019: 23 · 2018: 19 · 2017: 13
- FWCI
- 1.66
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- Locations
- Redox Biology (publishedVersion, cc-by-nc-nd)
- Europe PMC (PubMed Central) (publishedVersion, cc-by-nc-nd)
- PubMed Central (publishedVersion, cc-by-nc-nd)
- PubMed (publishedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Genomics, phytochemicals, and oxidative stress
- Health Sciences › Medicine › Rehabilitation › Exercise and Physiological Responses
- Health Sciences › Medicine › Complementary and alternative medicine › Cardiovascular and exercise physiology
- Keywords
- Nrf2, physical activity, oxidative stress, antioxidant defense, redox adaptation, acute exercise, regular exercise, cytoprotective genes, transcription factor signaling, skeletal muscle, myocardium
- MeSH terms
- Antioxidants, Humans, Myocardium, Organ Specificity, Oxidation-Reduction, Signal Transduction, Exercise, Up-Regulation, Reactive Oxygen Species, Muscle, Skeletal, NF-E2-Related Factor 2
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 ›
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