Exercise-induced oxidative stress: Friend or foe?
Open accessAbstract
The first report demonstrating that prolonged endurance exercise promotes oxidative stress in humans was published more than 4 decades ago. Since this discovery, many ensuing investigations have corroborated the fact that muscular exercise increases the production of reactive oxygen species (ROS) and results in oxidative stress in numerous tissues including blood and skeletal muscles. Although several tissues may contribute to exercise-induced ROS production, it is predicted that muscular contractions stimulate ROS production in active muscle fibers and that skeletal muscle is a primary source of ROS production during exercise. This contraction-induced ROS generation is associated with (1) oxidant damage in several tissues (e.g., increased protein oxidation and lipid peroxidation), (2) accelerated muscle fatigue, and (3) activation of biochemical signaling pathways that contribute to exercise-induced adaptation in the contracting muscle fibers. While our understanding of exercise and oxidative stress has advanced rapidly during the last decades, questions remain about whether exercise-induced increases in ROS production are beneficial or harmful to health. This review addresses this issue by discussing the site(s) of oxidant production during exercise and detailing the health consequences of exercise-induced ROS production.
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?
Muscle exercise increases production of ROS such as H2O2, leading to oxidative stress in many tissues, including skeletal muscle.
“Muscle exercise increases the production of ROS (e.g., hydrogen peroxide (H2O2)), leading to oxidative stress in many tissues, including skeletal muscle [52].”
From Exerkines and Sarcopenia: Unveiling the Mechanism Behind Exercise-Induced Mitochondrial Homeostasis (2025) · cites this paper as [52]
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
Free radicals in biology and medicine
Gutteridge, J. M. C. (1991) · General Pharmacology The Vascular System · doi:10.1016/0306-3623(91)90478-o · Cited by 17,178 · see citing works
Free Radicals in the Physiological Control of Cell Function
Dröge, W. (2002) · Physiological Reviews · doi:10.1152/physrev.00018.2001 · Cited by 9,855 · see citing works
Free radicals, metals and antioxidants in oxidative stress-induced cancer
Valko, M., Rhodes, C. J., Moncol, J., Izakovic, M., & Mazur, M. (2006) · Chemico-Biological Interactions · doi:10.1016/j.cbi.2005.12.009 · Cited by 6,680 · see citing works
Mitochondrial Dysfunction and Oxidative Stress in Neurodegenerative Diseases
Lin, M. T., & Beal, M. F. (2006) · Nature · doi:10.1038/nature05292 · Cited by 6,455 · see citing works
Nitric oxide synthases: regulation and function
Forstermann, U., & Sessa, W. C. (2012) · European Heart Journal · doi:10.1093/eurheartj/ehr304 · Cited by 4,409 · see citing works
Oxidative stress, aging, and diseases
Liguori, I., Russo, G., Curcio, F., Bulli, G., Aran, L., Della-Morte, D., Gargiulo, G., Testa, G., Cacciatore, F., Bonaduce, D., et al. (2018) · Clinical Interventions in Aging · doi:10.2147/cia.s158513 · Cited by 3,979 · see citing works
Neurodegenerative diseases and oxidative stress
Barnham, K. J., Masters, C. L., & Bush, A. I. (2004) · Nature Reviews Drug Discovery · doi:10.1038/nrd1330 · Cited by 3,683 · see citing works
Boveris, A., & Chance, B. (1973) · Biochemical Journal · doi:10.1042/bj1340707 · Cited by 2,626 · see citing works
Physiological functions of thioredoxin and thioredoxin reductase
Arnér, E. S. J., & Holmgren, A. (2000) · European Journal of Biochemistry · doi:10.1046/j.1432-1327.2000.01701.x · Cited by 2,535 · see citing works
Exercise-Induced Oxidative Stress: Cellular Mechanisms and Impact on Muscle Force Production
Powers, S. K., & Jackson, M. J. (2008) · Physiological Reviews · doi:10.1152/physrev.00031.2007 · Cited by 2,459 · see citing works
Self-citationTranscriptional Regulation by Nrf2
Tonelli, C., Chio, I. I. C., & Tuveson, D. A. (2017) · Antioxidants and Redox Signaling · doi:10.1089/ars.2017.7342 · Cited by 2,206 · see citing works
Blair, S. N. (1996) · JAMA: The Journal of the American Medical Association · doi:10.1001/jama.1996.03540030039029 · Cited by 1,819 · see citing works
Physical activity and survival after breast cancer diagnosis
Holmes, M. D. (2005) · JAMA · doi:10.1001/jama.293.20.2479 · Cited by 1,772 · see citing works
Free radicals and tissue damage produced by exercise
Davies, K. J. A., Quintanilha, A. T., Brooks, G. A., & Packer, L. (1982) · Biochemical and Biophysical Research Communications · doi:10.1016/s0006-291x(82)80124-1 · Cited by 1,739 · see citing works
Jones, D. P. (2006) · Antioxidants & Redox Signaling · doi:10.1089/ars.2006.8.1865 · Cited by 1,726 · 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
Association of Leisure-Time Physical Activity With Risk of 26 Types of Cancer in 1.44 Million Adults
Moore, S. C., Lee, I.-M., Weiderpass, E., Campbell, P. T., Sampson, J. N., Kitahara, C. M., Keadle, S. K., Arem, H., Berrington de Gonzalez, A., Hartge, P., et al. (2016) · JAMA Internal Medicine · doi:10.1001/jamainternmed.2016.1548 · Cited by 1,487 · see citing works
Mattson, M. P. (2008) · Ageing Research Reviews · doi:10.1016/j.arr.2007.08.007 · Cited by 1,253 · see citing works
Nitric oxide in skeletal muscle
Kobzik, L., Reid, M. B., Bredt, D. S., & Stamler, J. S. (1994) · Nature · doi:10.1038/372546a0 · Cited by 955 · see citing works
Free radicals in biology and medicine
Lucy, J. A. (1985) · FEBS Letters · doi:10.1016/0014-5793(85)80903-0 · Cited by 908 · see citing works
Physical activity and survival after colorectal cancer diagnosis
Meyerhardt, J. A., Giovannucci, E. L., Holmes, M. D., Chan, A. T., Chan, J. A., Colditz, G. A., & Fuchs, C. S. (2006) · Journal of Clinical Oncology · doi:10.1200/jco.2006.06.0855 · Cited by 857 · 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
Oxidative Stress in Neurodegenerative Diseases: From Molecular Mechanisms to Clinical Applications
Liu, Z., Zhou, T., Ziegler, A. C., Dimitrion, P., & Zuo, L. (2017) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2017/2525967 · Cited by 810 · see citing works
Physical activity and all-cause mortality: what is the dose–response relation?
LEE, I.-M., & SKERRETT, P. J. (2001) · Medicine and Science in Sports and Exercise · doi:10.1097/00005768-200106001-00016 · Cited by 786 · see citing works
Exercise and the Cardiovascular System: Clinical Science and Cardiovascular Outcomes
Lavie, C. J., Arena, R., Swift, D. L., Johannsen, N. M., Sui, X., Lee, D.-C., Earnest, C. P., Church, T. S., O’Keefe, J. H., Milani, R. V., et al. (2015) · Circulation Research · doi:10.1161/circresaha.117.305205 · Cited by 782 · see citing works
Free Radicals in Biological Materials
Commoner, B., Townsend, J., & Pake, G. E. (1954) · Nature · doi:10.1038/174689a0 · Cited by 743 · see citing works
Physical activity, all-cause and cardiovascular mortality, and cardiovascular disease
KRAUS, W. E., POWELL, K. E., HASKELL, W. L., JANZ, K. F., CAMPBELL, W. W., JAKICIC, J. M., TROIANO, R. P., SPROW, K., TORRES, A., & PIERCY, K. L. (2019) · Medicine & Science in Sports & Exercise · doi:10.1249/mss.0000000000001939 · Cited by 671 · see citing works
Redox regulation of PI 3‐kinase signalling via inactivation of PTEN
Leslie, N. R., Bennett, D., Lindsay, Y. E., Stewart, H., Gray, A., & Downes, C. P. (2003) · The EMBO Journal · doi:10.1093/emboj/cdg513 · Cited by 614 · see citing works
Kenfield, S. A., Stampfer, M. J., Giovannucci, E., & Chan, J. M. (2011) · Journal of Clinical Oncology · doi:10.1200/jco.2010.31.5226 · Cited by 601 · see citing works
Molecular mechanisms linking exercise to cancer prevention and treatment
Hojman, P., Gehl, J., Christensen, J. F., & Pedersen, B. K. (2018) · Cell Metabolism · doi:10.1016/j.cmet.2017.09.015 · Cited by 600 · see citing works
Effects of exercise, vitamin E, and ozone on pulmonary function and lipid peroxidation
Dillard, C. J., Litov, R. E., SAVIN, W. M., Dumelin, E. E., & Tappel, A. L. (1978) · Journal of Applied Physiology · doi:10.1152/jappl.1978.45.6.927 · Cited by 561 · see citing works
Reactive Oxygen Species: Impact on Skeletal Muscle
Powers, S. K., Ji, L. L., Kavazis, A. N., & Jackson, M. J. (2011) · Comprehensive physiology · doi:10.1002/cphy.c100054 · Cited by 509 · see citing works
Self-citationActivation of superoxide dismutases: Putting the metal to the pedal
Culotta, V., Yang, M., & O’Halloran, T. V. (2006) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2006.05.003 · Cited by 509 · see citing works
Reactive oxygen in skeletal muscle. I. Intracellular oxidant kinetics and fatigue in vitro
Reid, M. B., Haack, K. E., Franchek, K. M., Valberg, P. A., Kobzik, L., & West, M.-Y. (1992) · Journal of Applied Physiology · doi:10.1152/jappl.1992.73.5.1797 · Cited by 492 · see citing works
Invited Review: Redox modulation of skeletal muscle contraction: what we know and what we don't
Reid, M. B. (2001) · Journal of Applied Physiology · doi:10.1152/jappl.2001.90.2.724 · Cited by 450 · see citing works
Reactive Oxygen Species Are Signalling Molecules for Skeletal Muscle Adaptation
Powers, S. K., Duarte, J., Kavazis, A. N., & Talbert, E. E. (2010) · Experimental Physiology · doi:10.1113/expphysiol.2009.050526 · Cited by 440 · see citing works
Self-citationAndrade, F. H., Reid, M. B., Allen, D. G., & Westerblad, H. (1998) · The Journal of Physiology · doi:10.1111/j.1469-7793.1998.565bn.x · Cited by 438 · see citing works
Exercise and hormesis: oxidative stress-related adaptation for successful aging
Radak, Z. O., Chung, H. Y., & Goto, S. (2005) · Biogerontology · doi:10.1007/s10522-004-7386-7 · Cited by 413 · see citing works
Impact of Cardiorespiratory Fitness on All-Cause and Disease-Specific Mortality: Advances Since 2009
Harber, M. P., Kaminsky, L. A., Arena, R. A., Blair, S. N., Franklin, B. A., MYERS, J. N., & Ross, R. (2017) · Progress in Cardiovascular Diseases · doi:10.1016/j.pcad.2017.03.001 · Cited by 413 · see citing works
Influence of exercise and fiber type on antioxidant enzyme activity in rat skeletal muscle
Powers, S. K., Criswell, D. S., Lawler, J., Ji, L. L., Martin, D., Herb, R. A., & Dudley, G. (1994) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.1994.266.2.r375 · Cited by 379 · see citing works
Self-citationKobzik, L., Stringer, B., Balligand, J., Reid, M. B., & Stamler, J. S. (1995) · Biochemical and Biophysical Research Communications · doi:10.1006/bbrc.1995.1824 · Cited by 376 · see citing works
Paillard, T., Rolland, Y., & Barreto, P. D. S. (2015) · Journal of Clinical Neurology · doi:10.3988/jcn.2015.11.3.212 · Cited by 366 · see citing works
Glutathione peroxidases and redox-regulated transcription factors
Brigelius‐Flohé, R. (2006) · Biological Chemistry · doi:10.1515/bc.2006.166 · Cited by 361 · see citing works
Exercise‐induced oxidative stress: past, present and future
Powers, S. K., Radak, Z. O., & Ji, L. L. (2016) · The Journal of Physiology · doi:10.1113/jp270646 · Cited by 361 · see citing works
Self-citationReactive oxygen and nitrogen species as intracellular signals in skeletal muscle
Powers, S. K., Talbert, E. E., & Adhihetty, P. J. (2011) · The Journal of Physiology · doi:10.1113/jphysiol.2010.201327 · Cited by 340 · see citing works
Self-citationFree radicals and muscle fatigue: of ROS, canaries, and the IOC
Reid, M. B. (2008) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2007.03.002 · Cited by 329 · see citing works
Type II skeletal myofibers possess unique properties that potentiate mitochondrial H2O2 generation
Anderson, E. J., & Neufer, P. D. (2005) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00402.2005 · Cited by 329 · see citing works
The Antioxidant Effect of Exercise: A Systematic Review and Meta-Analysis
Sousa, C. V., Sales, M. M., Rosa, T. D. S., Lewis, J. E., de Andrade, R. V., & Simões, H. G. (2016) · Sports Medicine · doi:10.1007/s40279-016-0566-1 · Cited by 328 · see citing works
Multiple Functions and Regulation of Mammalian Peroxiredoxins
Rhee, S. G., & Kil, I. S. (2017) · Annual Review of Biochemistry · doi:10.1146/annurev-biochem-060815-014431 · Cited by 324 · see citing works
NFκB and AP-1 mediate transcriptional responses to oxidative stress in skeletal muscle cells
Zhou, L. Z.-H., Johnson, A. P., & Rando, T. A. (2001) · Free Radical Biology and Medicine · doi:10.1016/s0891-5849(01)00719-5 · Cited by 323 · see citing works
N-acetylcysteine inhibits muscle fatigue in humans.
Reid, M. B., Stokić, D. S., Koch, S. M., Khawli, F. A., & Leis, A. A. (1994) · Journal of Clinical Investigation · doi:10.1172/jci117615 · Cited by 317 · see citing works
Ito, N., Rüegg, U. T., Kudō, A., Miyagoe‐Suzuki, Y., & Takeda, S. (2012) · Nature Medicine · doi:10.1038/nm.3019 · Cited by 315 · see citing works
Reactive oxygen in skeletal muscle. III. Contractility of unfatigued muscle
Reid, M. B., Khawli, F. A., & Moody, M. R. (1993) · Journal of Applied Physiology · doi:10.1152/jappl.1993.75.3.1081 · Cited by 297 · see citing works
Kruk, J., Aboul-Enein, H. Y., Kładna, A., & Bowser, J. E. (2019) · Free Radical Research · doi:10.1080/10715762.2019.1612059 · Cited by 292 · see citing works
Leeuwenburgh, C., Fiebig, R., Chandwaney, R. H., & Ji, L. (1994) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.1994.267.2.r439 · Cited by 289 · see citing works
Electron spin resonance studies of intact mammalian skeletal muscle
Jackson, M. J., Edwards, R. H. T., & Symons, M. C. R. (1985) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/0167-4889(85)90019-9 · Cited by 286 · see citing works
Antioxidant enzyme systems in rat liver and skeletal muscle
Ji, L. L., Stratman, F. W., & Lardy, H. A. (1988) · Archives of Biochemistry and Biophysics · doi:10.1016/0003-9861(88)90623-6 · Cited by 280 · see citing works
Chemical hormesis: its historical foundations as a biological hypothesis
Calabrese, E. J., & Baldwin, L. A. (2000) · Human & Experimental Toxicology · doi:10.1191/096032700678815585 · Cited by 278 · see citing works
Sakellariou, G. K., Vasilaki, A., Palomero, J., Kayani, A., Zibrik, L., McArdle, A., & Jackson, M. J. (2013) · Antioxidants & Redox Signaling · doi:10.1089/ars.2012.4623 · Cited by 276 · see citing works
McKenna, M. J., Medved, I., Goodman, C. A., Brown, M. J., Bjorksten, A. R., Murphy, K. T., Petersen, A. C., Sostaric, S. M., & Gong, X. (2006) · The Journal of Physiology · doi:10.1113/jphysiol.2006.115352 · Cited by 265 · see citing works
Anaerobic Exercise and Oxidative Stress: A Review
Bloomer, R. J., & Goldfarb, A. H. (2004) · Canadian Journal of Applied Physiology · doi:10.1139/h04-017 · Cited by 262 · see citing works
Reactive Oxygen Species and Protein Oxidation in Aging: A Look Back, A Look Ahead
Hensley, K., & Floyd, R. A. (2002) · Archives of Biochemistry and Biophysics · doi:10.1006/abbi.2001.2630 · Cited by 255 · see citing works
Powers, S. K., Hudson, M. B., Nelson, W. B., Talbert, E. E., Min, K., Szeto, H. H., Kavazis, A. N., & Smuder, A. J. (2011) · Critical Care Medicine · doi:10.1097/ccm.0b013e3182190b62 · Cited by 255 · see citing works
Leeuwenburgh, C., Hollander, J., Leichtweis, S. B., Griffiths, M. A., Gore, M. T., & Ji, L. (1997) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.1997.272.1.r363 · Cited by 250 · see citing works
Groussard, C., Rannou‐Bekono, F., Machefer, G., Chevanne, M., Vincent, S., Sergent, O., Cillard, J., & Gratas‐Delamarche, A. (2003) · European Journal of Applied Physiology · doi:10.1007/s00421-002-0767-1 · Cited by 246 · see citing works
Glutathione and antioxidant enzymes in skeletal muscle: effects of fiber type and exercise intensity
Ji, L., Fu, R., & Mitchell, E. W. (1992) · Journal of Applied Physiology · doi:10.1152/jappl.1992.73.5.1854 · Cited by 237 · see citing works
Effect of resistance exercise on free radical production
McBride, J. M., Kraemer, W. J., Triplett-McBride, T., et al. (1998) · Medicine & Science in Sports & Exercise · doi:10.1097/00005768-199801000-00010 · Cited by 236 · see citing works
Skeletal muscle oxidative capacity, antioxidant enzymes, and exercise training
Laughlin, M. H., Simpson, T., Sexton, W. L., Brown, O. R., Smith, J. K., & Korthuis, R. J. (1990) · Journal of Applied Physiology · doi:10.1152/jappl.1990.68.6.2337 · Cited by 223 · see citing works
Rigorous exercise training increases superoxide dismutase activity in ventricular myocardium
Powers, S. K., Criswell, D. S., Lawler, J., Martin, D., Lieu, F., Ji, L. L., & Herb, R. A. (1993) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.1993.265.6.h2094 · Cited by 223 · see citing works
Self-citationHypertension and physical exercise: The role of oxidative stress
Larsen, M. K., & Matchkov, V. V. (2016) · Medicina · doi:10.1016/j.medici.2016.01.005 · Cited by 223 · see citing works
High intensity training-induced changes in skeletal muscle antioxidant enzyme activity
Criswell, D. S., Powers, S. K., DODD, S. L., Lawler, J. M., Edwards, W., Renshler, K., & GRINTON, S. F. (1993) · Medicine & Science in Sports & Exercise · doi:10.1249/00005768-199310000-00009 · Cited by 220 · see citing works
Self-citationMolecular Characterization of a Superoxide-Generating NAD(P)H Oxidase in the Ventilatory Muscles
Javeshghani, D., Magder, S. A., Barreiro, E., Quinn, M. T., & Hussain, S. N. A. (2002) · American Journal of Respiratory and Critical Care Medicine · doi:10.1164/ajrccm.165.3.2103028 · Cited by 215 · see citing works
Marengo, J. J., Hidalgo, C., & Bull, R. (1998) · Biophysical Journal · doi:10.1016/s0006-3495(98)77840-3 · Cited by 212 · see citing works
Kavazis, A. N., Talbert, E. E., Smuder, A. J., Hudson, M. B., Nelson, W. B., & Powers, S. K. (2009) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2009.01.002 · Cited by 205 · see citing works
Self-citationHigh-Intensity Interval Exercise and Cerebrovascular Health: Curiosity, Cause, and Consequence
Lucas, S. J. E., Cotter, J. D., Brassard, P., & Bailey, D. M. (2015) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1038/jcbfm.2015.49 · Cited by 194 · see citing works
The Effects of Acute Exercise on Neutrophils and Plasma Oxidative Stress
Quindry, J. C., Stone, W. L., KING, J., et al. (2003) · Medicine & Science in Sports & Exercise · doi:10.1249/01.mss.0000074568.82597.0b · Cited by 179 · see citing works
Oxidative Stress, Diabetes, and Diabetic Complications
Wei, W., Liu, Q., Tan, Y., Liu, L., Li, X., & Cai, L. (2009) · Hemoglobin · doi:10.3109/03630260903212175 · Cited by 178 · see citing works
Exercise-induced hormesis and skeletal muscle health
Ji, L. L., Kang, C., & Zhang, Y. (2016) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2016.02.025 · Cited by 176 · see citing works
Effect of N-acetylcysteine on diaphragm fatigue
Shindoh, C., DiMarco, A. F., Thomas, A., Manubay, P., & Supinski, G. S. (1990) · Journal of Applied Physiology · doi:10.1152/jappl.1990.68.5.2107 · Cited by 174 · see citing works
Adams, V. (2002) · Cardiovascular Research · doi:10.1016/s0008-6363(02)00228-6 · Cited by 172 · see citing works
Exercise, oxidants, and antioxidants change the shape of the bell-shaped hormesis curve
Radak, Z. O., Ishihara, K., Tékus, É., Varga, C., Pósa, A., Balogh, L., Boldogh, I. R., & Koltai, E. (2017) · Redox Biology · doi:10.1016/j.redox.2017.02.015 · Cited by 171 · see citing works
Moopanar, T. R., & Allen, D. G. (2005) · The Journal of Physiology · doi:10.1113/jphysiol.2005.083519 · Cited by 165 · see citing works
Antioxidant and Adaptative Response Mediated by Nrf2 during Physical Exercise
Vargas-Mendoza, N., Morales‐González, Á., Madrigal‐Santillán, E., Madrigal‐Bujaidar, E., Álvarez‐González, I., García-Melo, L. F., Anguiano‐Robledo, L., Fregoso-Aguilar, T. A., & Morales‐González, J. A. (2019) · Antioxidants · doi:10.3390/antiox8060196 · Cited by 163 · see citing works
Jackson, M. J. (2007) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2007.06.003 · Cited by 161 · see citing works
Classes of Thiols That Influence the Activity of the Skeletal Muscle Calcium Release Channel
Sun, J., Xu, L., Eu, J. P., Stamler, J. S., & Meissner, G. (2001) · Journal of Biological Chemistry · doi:10.1074/jbc.m100083200 · Cited by 158 · see citing works
Espinosa, A., Leiva, A., Peña, M., Müller, M., Anibal Debandi, L., Hidalgo, C., Carrasco, M. A., & Jaimovich, E. (2006) · Journal of Cellular Physiology · doi:10.1002/jcp.20745 · Cited by 155 · see citing works
Regulation of NADPH oxidases in skeletal muscle
Ferreira, L. F., & Laitano, O. (2016) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2016.05.011 · Cited by 150 · see citing works
Selenium and the thioredoxin and glutaredoxin systems.
Björnstedt, M., Kumar, S., Björkhem, L., Spyrou, G. P., & Holmgren, A. (1997) · PubMed · Cited by 149 · see citing works
Mediators of Physical Activity Protection against ROS-Linked Skeletal Muscle Damage
Meo, S. D., Napolitano, G., & Venditti, P. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20123024 · Cited by 146 · see citing works
Control of Reactive Oxygen Species Production in Contracting Skeletal Muscle
Jackson, M. J. (2011) · Antioxidants and Redox Signaling · doi:10.1089/ars.2011.3976 · Cited by 145 · see citing works
Transmembrane Redox Sensor of Ryanodine Receptor Complex
Feng, W., Liu, G., Allen, P. D., & Pessah, I. N. (2000) · Journal of Biological Chemistry · doi:10.1074/jbc.c000523200 · Cited by 141 · see citing works
Oxidants and Skeletal Muscle Function: Physiologic and Pathophysiologic Implications
Clanton, T. L., Zuo, L., & Klawitter, P. F. (1999) · Proceedings of The Society for Experimental Biology and Medicine · doi:10.1046/j.1525-1373.1999.d01-142.x · Cited by 134 · see citing works
Skeletal muscle sarcoplasmic reticulum contains a NADH-dependent oxidase that generates superoxide
Xia, R., Webb, J. A., Gnall, L. L. M., Cutler, K., & Abramson, J. J. (2003) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00034.2002 · Cited by 129 · see citing works
Evolution of the thioredoxin system as a step enabling adaptation to oxidative stress
Balsera, M., & Buchanan, B. B. (2019) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2019.03.003 · Cited by 127 · see citing works
Lipoxygenase-dependent superoxide release in skeletal muscle
Zuo, L., Christofi, F. L., Wright, V. P., Bao, S., & Clanton, T. L. (2004) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00096.2004 · Cited by 123 · see citing works
Acute exercise and skeletal muscle antioxidant and metabolic enzymes: effects of fiber type and age
Lawler, J. M., Powers, S. K., Visser, T., et al. (1993) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.1993.265.6.r1344 · Cited by 118 · see citing works
Self-citationExercise-induced biochemical changes and their potential influence on cancer: a scientific review
Thomas, R., Kenfield, S. A., & Jiménez, A. (2016) · British Journal of Sports Medicine · doi:10.1136/bjsports-2016-096343 · Cited by 118 · see citing works
Spin-trappers and vitamin E prolong endurance to muscle fatigue in mice
Novelli, G. (1990) · Free Radical Biology and Medicine · doi:10.1016/0891-5849(90)90138-9 · Cited by 117 · see citing works
PLA2dependence of diaphragm mitochondrial formation of reactive oxygen species
Nethery, D. E., Callahan, L. A., Stofan, D. A., Mattera, R., DiMarco, A. F., & Supinski, G. S. (2000) · Journal of Applied Physiology · doi:10.1152/jappl.2000.89.1.72 · Cited by 115 · see citing works
Pearson, T., Kabayo, T., Ng, R., Chamberlain, J., McArdle, A., & Jackson, M. J. (2014) · PLoS ONE · doi:10.1371/journal.pone.0096378 · Cited by 107 · see citing works
Brotto, M. A. P., & Nosek, T. M. (1996) · Journal of Applied Physiology · doi:10.1152/jappl.1996.81.2.731 · Cited by 107 · see citing works
Short-term exercise training improves diaphragm antioxidant capacity and endurance
Vincent, H. K., Powers, S. K., Stewart, D. J., Demirel, H. A., Shanely, R. A., & Naıto, H. (2000) · European Journal of Applied Physiology and Occupational Physiology · doi:10.1007/pl00013799 · Cited by 106 · see citing works
Self-citationCytosolic Phospholipase A2 (cPLA2) Regulation of Human Monocyte NADPH Oxidase Activity
Zhao, X., Bey, E. A., Wientjes, F. B., & Cathcart, M. K. (2002) · Journal of Biological Chemistry · doi:10.1074/jbc.m203630200 · Cited by 104 · see citing works
Regional training-induced alterations in diaphragmatic oxidative and antioxidant enzymes
Powers, S. K., Criswell, D. S., Lawler, J. M., Martin, D., Ji, L. L., Herb, R. A., & Dudley, G. (1994) · Respiration Physiology · doi:10.1016/0034-5687(94)90118-x · Cited by 101 · see citing works
Self-citationGong, M. C., Arbogast, S., Guo, Z., Mathenia, J., Su, W., & Reid, M. B. (2005) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00873.2005 · Cited by 96 · see citing works
Nocella, C., Cammisotto, V., Pigozzi, F., Borrione, P., FOSSATI, C., D’Amico, A., Cangemi, R., Peruzzi, M., Gobbi, G., Ettorre, E., et al. (2019) · Nutrients · doi:10.3390/nu11061353 · Cited by 96 · see citing works
Exercise volume and intensity: a dose–response relationship with health benefits
Foulds, H. J. A., Bredin, S. S. D., Charlesworth, S. A., Ivey, A. C., & Warburton, D. E. R. (2014) · European Journal of Applied Physiology · doi:10.1007/s00421-014-2887-9 · Cited by 95 · see citing works
Formation of reactive oxygen species by the contracting diaphragm is PLA2dependent
Nethery, D. E., Stofan, D. A., Callahan, L. A., DiMarco, A. F., & Supinski, G. S. (1999) · Journal of Applied Physiology · doi:10.1152/jappl.1999.87.2.792 · Cited by 92 · see citing works
DNA Damage Following Acute Aerobic Exercise: A Systematic Review and Meta-analysis
Tryfidou, D. V., McClean, C. M., Nikolaidis, M. G., & Davison, G. W. (2019) · Sports Medicine · doi:10.1007/s40279-019-01181-y · Cited by 91 · see citing works
Chemical Hormesis: Its Historical Foundations as a Biological Hypothesis
Calabrese, E. J., & Baldwin, L. A. (1999) · Toxicologic Pathology · doi:10.1177/019262339902700207 · Cited by 90 · see citing works
Mechanical Stretch-Induced Activation of ROS/RNS Signaling in Striated Muscle
Ward, C. W., Prosser, B. L., & Lederer, W. J. (2013) · Antioxidants and Redox Signaling · doi:10.1089/ars.2013.5517 · Cited by 87 · see citing works
Redox interventions to increase exercise performance
Reid, M. B. (2015) · The Journal of Physiology · doi:10.1113/jp270653 · Cited by 85 · see citing works
Cellular mechanisms underlying oxidative stress in human exercise
Jackson, M. J., Vasilaki, A., & McArdle, A. (2016) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2016.02.023 · Cited by 83 · see citing works
Posterino, G. S., Cellini, M. A., & Lamb, G. D. (2003) · The Journal of Physiology · doi:10.1111/j.1469-7793.2003.00807.x · Cited by 81 · see citing works
Impact of different resistance training protocols on muscular oxidative stress parameters
Scheffer, D. D. L., da Silva, L. A., Tromm, C. B., da Rosa, G. L., Silveira, P. C. L., de Souza, C. T., Latini, A., & Pinho, R. A. (2012) · Applied Physiology Nutrition and Metabolism · doi:10.1139/h2012-115 · Cited by 79 · see citing works
Mitochondrial redox potential during contraction in single intact muscle fibers
Michaelson, L. P., Shi, G., Ward, C. W., & Rodney, G. G. (2010) · Muscle & Nerve · doi:10.1002/mus.21724 · Cited by 79 · see citing works
Endurance exercise attenuates ventilator-induced diaphragm dysfunction
Smuder, A. J., Min, K., Hudson, M. B., Kavazis, A. N., Kwon, O., Nelson, W. B., & Powers, S. K. (2011) · Journal of Applied Physiology · doi:10.1152/japplphysiol.01086.2011 · Cited by 75 · see citing works
Self-citationExercise-Induced Mitohormesis for the Maintenance of Skeletal Muscle and Healthspan Extension
Musci, R., Hamilton, K., & Linden, M. (2019) · Sports · doi:10.3390/sports7070170 · Cited by 73 · see citing works
Hearn, A. S., Tu, C., Nick, H. S., & Silverman, D. N. (1999) · Journal of Biological Chemistry · doi:10.1074/jbc.274.35.24457 · Cited by 72 · see citing works
Supinski, G. S., Stofan, D. A., Ciufo, R., & DiMarco, A. F. (1997) · Journal of Applied Physiology · doi:10.1152/jappl.1997.82.4.1119 · Cited by 59 · see citing works
Posterino, G. S., Cellini, M. A., & Lamb, G. D. (2003) · The Journal of Physiology · doi:10.1113/jphysiol.2002.035204 · Cited by 59 · see citing works
Exercise training protects against contraction-induced lipid peroxidation in the diaphragm
Vincent, H. K., Powers, S. K., Demirel, H. A., Coombes, J. S., & Naıto, H. (1999) · European Journal of Applied Physiology · doi:10.1007/s004210050505 · Cited by 57 · see citing works
Self-citationAn unexplored role for Peroxiredoxin in exercise-induced redox signalling?
Wadley, A. J., Aldred, S., & Coles, S. (2015) · Redox Biology · doi:10.1016/j.redox.2015.10.003 · Cited by 54 · see citing works
Redox homeostasis and age‐related deficits in neuromuscular integrity and function
Sakellariou, G. K., Lightfoot, A. P., Earl, K. E., Stofanko, M., & McDonagh, B. (2017) · Journal of Cachexia Sarcopenia and Muscle · doi:10.1002/jcsm.12223 · Cited by 49 · see citing works
Superoxide dismutases in exercise and disease
Suzuki, K., Ohno, H., Oh‐ishi, S., Kizaki, T., Ookawara, T., Fujii, J., Radak, Z. O., & Taniguchi, N. (2000) · Elsevier eBooks · doi:10.1016/b978-044482650-3/50011-0 · Cited by 47 · see citing works
Balke, J. E., Zhang, L., & Percival, J. M. (2018) · Nitric Oxide · doi:10.1016/j.niox.2018.11.004 · Cited by 44 · see citing works
Resistance Training, Antioxidant Status, and Antioxidant Supplementation
Ismaeel, A., Holmes, M., Papoutsi, E., Panton, L. B., & Koutakis, P. (2019) · International Journal of Sport Nutrition and Exercise Metabolism · doi:10.1123/ijsnem.2018-0339 · Cited by 37 · see citing works
Antioxidant Supplementation and Adaptive Response to Training: A Systematic Review
Pastor, R., & Tur, J. A. (2019) · Current Pharmaceutical Design · doi:10.2174/1381612825666190701164923 · Cited by 33 · see citing works
Redox Mechanisms of Muscle Dysfunction in Inflammatory Disease
Reid, M. B., Andrade, F. H., Balke, C. W., & Esser, K. A. (2005) · Physical Medicine and Rehabilitation Clinics of North America · doi:10.1016/j.pmr.2005.08.016 · Cited by 25 · see citing works
Flagged first, then by citations
Research works printed but not linked: 1
- [7]Sies H. Oxidative stress 1985 Academic Press London
Cited by
Sorted by citations
Gaitán, J. M., Moon, H. Y., Stremlau, M., Dubal, D. B., Cook, D. B., Okonkwo, O. C., & van Praag, H. (2021) · Frontiers in Endocrinology · doi:10.3389/fendo.2021.660181 · Cited by 160 · see citing works
Exercise-Mediated Browning of White Adipose Tissue: Its Significance, Mechanism and Effectiveness
Mu, W.-J., Zhu, J.-Y., Chen, M., & Guo, L. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms222111512 · Cited by 99 · see citing works
Granata, C., Caruana, N. J., Botella, J., Jamnick, N. A., Huynh, K., Kuang, J., Janssen, H. A., Reljic, B., Mellett, N. A., Laskowski, A., et al. (2021) · Nature Communications · doi:10.1038/s41467-021-27153-3 · Cited by 93 · see citing works
Reflections of an aging free radical
Halliwell, B. (2020) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2020.10.010 · Cited by 75 · see citing works
Calella, P., Cerullo, G., Di Dio, M., Liguori, F., Di Onofrio, V., Gallè, F., & Liguori, G. (2022) · Frontiers in Nutrition · doi:10.3389/fnut.2022.1048258 · Cited by 69 · see citing works
Age-associated inflammation and implications for skeletal muscle responses to exercise
Kunz, H. E., & Lanza, I. R. (2023) · Experimental Gerontology · doi:10.1016/j.exger.2023.112177 · Cited by 56 · see citing works
Exerkines and Sarcopenia: Unveiling the Mechanism Behind Exercise-Induced Mitochondrial Homeostasis
Wang, J., Jia, D., Zhang, Z., & Wang, D. (2025) · Metabolites · doi:10.3390/metabo15010059 · Cited by 23 · see citing works
Small peptides: Could they have a big role in metabolism and the response to exercise?
Atakan, M. M., Türkel, İ., Özerkliğ, B., Koşar, Ş. N., Taylor, D. F., Yan, X., & Bishop, D. J. (2024) · The Journal of Physiology · doi:10.1113/jp283214 · Cited by 13 · see citing works
Kamel, M., Aleya, S., Louzon, M., & Aleya, L. (2025) · Archives of Toxicology · doi:10.1007/s00204-025-04113-0 · Cited by 2 · see citing works
- Authors
- Powers, S. K., Deminice, R., Ozdemir, M., Yoshihara, T., Bomkamp, M. P., & Hyatt, H.
- Affiliations
- University of Florida (US)
- Universidade Estadual de Londrina (BR)
- Corresponding author
- Ozdemir, Mustafa
- ORCID
- Venue
- Journal of Sport and Health Science
- Publisher
- Elsevier BV
- Published
- 2020-09
- Volume
- 9
- Issue
- 5
- Pages
- 415-425
- ISSN
- 2213-2961 (ISSN-L)
- 2095-2546
- PMC
- PMC7498668
- OpenAlex
- W3022014008
- Cited by
- 655
- References
- 129
- Citations by year
- 2026: 93 · 2025: 135 · 2024: 121 · 2023: 129 · 2022: 103 · 2021: 68 · 2020: 6
- FWCI
- 9.40
- Type
- journal article
- Language
- en
- Open access
- diamond
- doi.org
- Licence
- Locations
- Journal of sport and health science/Journal of Sport and Health Science (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)
- Funders
- Japan Society for the Promotion of Science (17K01765, 23K20366)
- Topics
- Health Sciences › Medicine › Rehabilitation › Exercise and Physiological Responses
- Health Sciences › Medicine › Biochemistry › Antioxidant Activity and Oxidative Stress
- Health Sciences › Medicine › Complementary and alternative medicine › Cardiovascular and exercise physiology
- Keywords
- exercise-induced oxidative stress, reactive oxygen species, skeletal muscle, muscle contraction, protein oxidation, lipid peroxidation, muscle fatigue, exercise adaptation
- MeSH terms
- Adaptation, Physiological, Animals, Antioxidants, Humans, Muscle Contraction, Oxidation-Reduction, Exercise, Reactive Oxygen Species, Oxidative Stress, Muscle, Skeletal, Muscle Fibers, Skeletal, Muscle Fatigue
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