The DOI matches its Crossref record; 10 of the 10 references it cites were found in a registry or an index.
Do antioxidant supplements interfere with skeletal muscle adaptation to exercise training?
Open accessAbstract
A popular belief is that reactive oxygen species (ROS) and reactive nitrogen species (RNS) produced during exercise by the mitochondria and other subcellular compartments ubiquitously cause skeletal muscle damage, fatigue and impair recovery. However, the importance of ROS and RNS as signals in the cellular adaptation process to stress is now evident. In an effort to combat the perceived deleterious effects of ROS and RNS it has become common practice for active individuals to ingest supplements with antioxidant properties, but interfering with ROS/RNS signalling in skeletal muscle during acute exercise may blunt favourable adaptation. There is building evidence that antioxidant supplementation can attenuate endurance training‐induced and ROS/RNS‐mediated enhancements in antioxidant capacity, mitochondrial biogenesis, cellular defence mechanisms and insulin sensitivity. However, this is not a universal finding, potentially indicating that there is redundancy in the mechanisms controlling skeletal muscle adaptation to exercise, meaning that in some circumstances the negative impact of antioxidants on acute exercise response can be overcome by training. Antioxidant supplementation has been more consistently reported to have deleterious effects on the response to overload stress and high‐intensity training, suggesting that remodelling of skeletal muscle following resistance and high‐intensity exercise is more dependent on ROS/RNS signalling. Importantly there is no convincing evidence to suggest that antioxidant supplementation enhances exercise‐training adaptions. Overall, ROS/RNS are likely to exhibit a non‐linear (hormetic) pattern on exercise adaptations, where physiological doses are beneficial and high exposure (which would seldom be achieved during normal exercise training) may be detrimental. image
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“However, chronic high-dose antioxidant supplementation (such as vitamin E and C and curcumin) could blunt training adaptations by attenuating the necessary oxidative and inflammatory responses to exercise [84].”
From Use of Nutritional Strategies, Bioactive Compounds, and Dietary Supplements in Young Athletes: From Evidence to Potential Risks—A Narrative Review (2025) · cites this paper as [84]
In the citing paper
“Merry and Ristow (47) state that, while antioxidants could play a role in recovery, vitamin C may reduce muscle hypertrophy signaling, in addition to hampering the athlete's ability to adapt to exercise training (31).”
From Micronutrient supplement intakes among collegiate and masters athletes: A cross-sectional study (2023) · cites this paper as [47]
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Cites
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Targeting Antioxidants to Mitochondria by Conjugation to Lipophilic Cations
Murphy, M. P., & Smith, R. A. J. (2007) · Annual Review of Pharmacology and Toxicology · doi:10.1146/annurev.pharmtox.47.120505.105110 · Cited by 1,173
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Reactive oxygen species enhance insulin sensitivity
Loh, K., Deng, H., Fukushima, A., Cai, X., Boivin, B., Galic, S., Bruce, C., Shields, B. J., Skiba, B., Ooms, L. M., et al. (2009) · Cell Metabolism · doi:10.1016/j.cmet.2009.08.009 · Cited by 581
Unraveling the Truth About Antioxidants: Mitohormesis explains ROS-induced health benefits
Ristow, M. (2014) · Nature Medicine · doi:10.1038/nm.3624 · Cited by 417 · cited 6×
“This is consistent with hormesis, whereby favourable biological adaptations occur in response to low continuous or higher intermitted exposure to a stressor that would be harmful at large or chronic doses (Ristow, 2014; Yun & Finkel, 2014).”
BackgroundInfluentialSelf-citationFischer, C. P., Hiscock, N. J., Penkowa, M., Basu, S., Vessby, B., Kallner, A., Sjöberg, L., & Pedersen, B. K. (2004) · The Journal of Physiology · doi:10.1113/jphysiol.2004.066779 · Cited by 293 · cited 1×
“…in inflammatory markers and cytokines (Peake et al. 2007) including interleukin 6 (IL-6) and tumour necrosis factor (TNF) (Vassilakopoulos et al. 2003; Fischer et al. 2004), although this is not seen by all (Aguilo et al. 2007; Teixeira et al. 2009; Yfanti et al. 2010; Bailey et al. 2011).”
BackgroundYfanti, C., Nielsen, A. R., Åkerström, T., Nielsen, S., Rose, A. J., Richter, E. A., Lykkesfeldt, J., Fischer, C. P., & Pedersen, B. K. (2011) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00207.2010 · Cited by 85
Cobley, J. N., McGlory, C., Morton, J. P., & Close, G. L. (2011) · International Journal of Sport Nutrition and Exercise Metabolism · doi:10.1123/ijsnem.21.6.451 · Cited by 76
Vitamin C Administration Attenuates Overload-Induced Skeletal Muscle Hypertrophy in Rats
Makanae, Y., Kawada, S., Sasaki, K., Nakazato, K., & Ishii, N. (2013) · Acta Physiologica · doi:10.1111/apha.12042 · Cited by 59
Cited by
Skeletal muscle energy metabolism during exercise
Hargreaves, M., & Spriet, L. L. (2020) · Nature Metabolism · doi:10.1038/s42255-020-0251-4 · Cited by 1,408
Dzik, K. P., & Kaczor, J. J. (2019) · European Journal of Applied Physiology · doi:10.1007/s00421-019-04104-x · Cited by 357
Merry, T. L., & Ristow, M. (2016) · The Journal of Physiology · doi:10.1113/jp271957 · Cited by 246
Self-citationFruit-Derived Polyphenol Supplementation for Athlete Recovery and Performance
Bowtell, J., & Kelly, V. (2019) · Sports Medicine · doi:10.1007/s40279-018-0998-x · Cited by 213
Reynolds, J. C., Lai, R. W., Woodhead, J. S. T., Joly, J. H., Mitchell, C. J., Cameron-Smith, D., Lu, R., Cohen, P., Graham, N. A., Benayoun, B. A., et al. (2021) · Nature Communications · doi:10.1038/s41467-020-20790-0 · Cited by 199
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Metadata
- Authors
- Merry, T. L., & Ristow, M.
- Venue
- The Journal of Physiology
- Publisher
- Wiley
- Published
- 2016-01-18
- Volume
- 594
- Issue
- 18
- Pages
- 5135-5147
- ISSN
- 0022-3751 (ISSN-L)
- 1469-7793
- OpenAlex
- W2190841046
- Cited by
- 316
- References
- 10
- FWCI
- 13.61
- Type
- journal article
- Language
- en
- Open access
- green
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