No retraction, correction or concern found when last checked on Oct 17, 2026.
Oxidative Stress: Concept and Some Practical Aspects
Helmut Sies
Antioxidants · 2020 · CC BY
Abstract
Oxidative stress is defined as “an imbalance between oxidants and antioxidants in favor of the oxidants, leading to a disruption of redox signaling and control and/or molecular damage”. This Commentary presents basic features of this global concept which has attracted interest in biology and medicine. The term “antioxidants” in cellular defense against oxidants predominantly includes antioxidant enzymes with their substrates and coenzymes. Exogenous low-molecular-mass compounds also have a role, but this is more limited. Multiple biomarkers of damage due to oxidative stress have been identified for different molecular classes (protein, lipid, carbohydrate, and DNA), and the current state of practical aspects in health and disease is delineated.
Full text
From PubMed Central, U.S. National Library of Medicine, as current on Oct 17, 2026. Paragraph numbers are ours, so an answer can point at one.
1. Introduction
“Oxidative stress” is a global concept in redox biology and medicine. Since its introduction in 1985, it has attracted widespread interest and also some critical comments, and it is covered in detail in a textbook (pp. 199–283). The literature on oxidative stress is voluminous, and comprehensive coverage is not the subject of this Commentary; for example, the active fields of oxidative stress research in microbes and in plants are not covered, but the general principles apply to these fields as well. Rather, an attempt will be made to address the current state of knowledge in terms of practical aspects. Due to the multitude of oxidant and antioxidant processes occurring simultaneously in normal and pathophysiological conditions in different cells and organs, there have been numerous endeavors of translational application in a wide range of health and disease situations. Some of these have been based on oversimplifications. I will address this issue with some examples, focusing on recent literature.
2. Oxidative Stress
A brief survey of the literature in the Web of Science gives over 450,000 hits for the term “oxidative stress”, with about 40,000 new additions in 2020. Unsurprisingly, a comprehensive view on the current development of this term would be challenging.
2.1. The Concept of Oxidative Stress
The global concept of “Oxidative Stress” is defined as “an imbalance between oxidants and antioxidants in favor of the oxidants, leading to a disruption of redox signaling and control and/or molecular damage”. It has developed from its initial formulation in 1985 to incorporate new knowledge on the role of redox signaling. The basic idea is that, in the open metabolic system, a steady-state redox balance is maintained at a given setpoint, which provides a basal redox tone, and that a deviation from the steady-state redox balance is considered a stress, initiating a stress response. Implicit in the definition of oxidative stress is (i) that a deviation to the opposite side of the balance is “reductive stress”, and (ii) that there are physiological deviations, “oxidative eustress”, and supraphysiological deviations, “oxidative distress”. Oxidative eustress is an essential part of redox control and physiological redox signaling (Figure 1). This concept overlaps with that of redox homeostasis as the “golden mean”. Current knowledge on these topics has been presented in the book, “Oxidative stress: eustress and distress”.
2.2. Oxidative Stress: A Slice of the Pie
The molecular mechanisms of metabolic regulation include a multitude of chemical means. Structure and functions are implemented by orchestrated chemical modification of proteins, lipids, carbohydrates, and, not-the-least, nucleic acids. Redox reactions contribute to regulation, and it is noteworthy that there is crosstalk between different modes of regulation, e.g., between redox modifications and phosphorylation/dephosphorylation of proteins. Chemically reactive molecules of low-molecular-mass (“reactive species”) have been extensively investigated in their role in regulation. Recent accounts were given for reactive oxygen species (ROS), reactive nitrogen species (RNS), reactive sulfur species (RSS), reactive electrophile species (RES), and reactive halogen species (RHS). Clearly, multiple interactions constitute checks and balances in redox regulation.
3. Antioxidants
On the other side of the redox balance, the defense against damaging levels of oxidants consists of several types of antioxidant enzymes in conjunction with their back-up systems, as well as of low-molecular-mass antioxidants, forming an antioxidant network. The complement of antioxidant enzymes is subject to regulation by redox master switches as part of the oxidative stress response (see Ref. for a review). While these two preceding sentences appear to be uncontested, a widespread misconception about “antioxidants” and “antioxidant capacity” deserves a comment. In lay language, the term antioxidant seems to be confined solely to exogenous low-molecular-mass compounds, neglecting the much more important contribution of antioxidant enzymes (with their substrates and coenzymes) to cellular defense against oxidants. This misconception also pervades in the scientific community, best exemplified by the term “antioxidant capacity”, or even “total antioxidant capacity (TAC)”. The misconception can be traced back to the work of excellent organic chemists, who investigated the capability of isolated human blood plasma to trap artificially generated peroxyl radicals. This was the origin of the term “total antioxidant capacity” which, while true for isolated plasma in vitro, unfortunately is a misnomer as it was subsequently applied to the in vivo situation by many investigators. Such tests (TRAP, FRAP, ORAC, ABTS) do not assay any antioxidant enzyme capacity, and a more appropriate name instead of TAC would have been NEAC, non-enzymatic antioxidant capacity.
In their textbook, Halliwell and Gutteridge devoted a chapter to antioxidants synthesized in vivo (pp. 77–152) and a separate one on antioxidants from the diet (pp. 153–198), emphasizing the points made above: “Antioxidant is a term widely used but surprisingly difficult to define clearly”, and the simplified definition is “any substance that delays, prevents or removes oxidative damage to a target molecule” (p. 77). Hopefully, the distinction between endogenous and exogenous antioxidants will guide more prudent research in the future.
4. Practical Aspects
Against this background, it is obvious that oxidative stress will have different intensities and manifestations in different cell types and organs, as discussed previously. The set of principles which defines the spatiotemporal positioning of the biological redox systems has been described as the “redox code”. Redox patterns across cells and within subcellular spaces resemble a dynamic “landscape” rather than being flat.
4.1. Biomarkers
In accordance with the variety of compounds and pathways, numerous biomarkers of oxidative stress have been identified. Frijhoff et al. examined the relevance of specific biomarkers of oxidative stress in various diseases, as depicted in a cluster analysis (Figure 2).
Obviously, measuring a single biomarker is not clinically useful. The epistemological challenges of using such biomarkers have been discussed. Ghezzi proposed a classification of biomarkers of oxidative stress (Table 1), which may help guide researchers in the field. A specific term worth pursuing further is “actionability of oxidative stress biomarkers”, i.e., whether a given biomarker is causally involved in the disease or not. Advances in technology provide further opportunities for biomarkers, e.g., in redox phospholipidomics, proteomics, amino acids, protein lipoxidation, or metabolomics. Gender- and age-dependencies of different oxidative stress biomarkers have been noted.
4.2. Clinical Aspects
There is a wide literature of oxidative stress manifestation in clinical settings, as presented in pertinent reviews. In-depth discussion of these aspects is beyond the scope of this Commentary (see). A promising emerging area for research relates to mind-body medicine, the relationship between psychological stress and oxidative stress. Our recent coverage on oxidative stress manifestation in clinical settings is on the following topics: central nervous system; immune system, inflammation and wound repair; cardiovascular system; skeletal muscle; insulin sensitivity and pathogenesis of diabetes; ROS in aging and lifespan regulation; cancer; and prospects for redox medicine. Redox systems analysis of antioxidant networks will help to further understand the interplay of nutrition and oxidative stress.
5. Conclusions
Understanding the mechanisms of maintenance of the redox balance has progressed in recent time, opening opportunities for redox-based strategies in practical applications in medicine (“redox medicine”). Due to the complexity of interlinked stress response systems, future research will focus on redox systems biology.
References 44
- 1.
Sies H. Oxidative stress: Introductory remarks. Oxidative Stress. 1985;1-8.
Not in our library
- 2.
Sies H. On the history of oxidative stress: Concept and some aspects of current development. Curr. Opin. Toxicol. 2018;7:122-126.
Not in our library10.1016/j.cotox.2018.01.002
- 3.
Halliwell B., Gutteridge J.M.C. Free Radicals in Biology and Medicine. 2015.
Not in our library
- 4.
Sies H., Jones D.P., Fink G. Oxidative stress. Encyclopedia of Stress. 2007;Volume 3:45-48.
Not in our library
- 5.
Sies H., Berndt C., Jones D.P. Oxidative stress. Annu. Rev. Biochem. 2017;86:715-748.
Not in our library10.1146/annurev-biochem-061516-045037
- 6.
- 7.
Sies H., Jones D.P. Reactive oxygen species (ROS) as pleiotropic physiological signalling agents. Nat. Rev. Mol. Cell Biol. 2020;21:363-383.
Not in our library10.1038/s41580-020-0230-3
- 8.
Ursini F., Maiorino M., Forman H.J. Redox homeostasis: The Golden Mean of healthy living. Redox. Biol. 2016;8:205-215.
Not in our library10.1016/j.redox.2016.01.010
- 9.
Sies H. Oxidative Stress: Eustress and Distress. 2020;1-844.
Not in our library
- 10.
Möller M.N., Rios N., Trujillo M., Radi R., Denicola A., Alvarez B. Detection and quantification of nitric oxide-derived oxidants in biological systems. J. Biol. Chem. 2019;294:14776-14802.
Not in our library10.1074/jbc.rev119.006136
- 11.
Nakamura T., Lipton S.A. Nitric oxide-dependent protein post-translational modifications impair mitochondrial function and metabolism to contribute to neurodegenerative diseases. Antioxid. Redox Signal. 2020;32:817-833.
Not in our library10.1089/ars.2019.7916
- 12.
Olson K.R. Reactive oxygen species or reactive sulfur species: Why we should consider the latter. J. Exp. Biol. 2020;223:jeb196352.
Not in our library10.1242/jeb.196352
- 13.
Parvez S., Long M.J.C., Poganik J.R., Aye Y. Redox signaling by reactive electrophiles and oxidants. Chem. Rev. 2018;118:8798-8888.
Not in our library10.1021/acs.chemrev.7b00698
- 14.
Davies M.J., Hawkins C.L. The role of myeloperoxidase in biomolecule modification, chronic inflammation, and disease. Antioxid. Redox Signal. 2020;32:957-981.
Not in our library10.1089/ars.2020.8030
- 15.
Santolini J., Wootton S.A., Jackson A.A., Feelisch M. The redox architecture of physiological function. Curr. Opin. Physiol. 2019;9:34-47.
Not in our library10.1016/j.cophys.2019.04.009
- 16.
Sies H. Strategies of antioxidant defense. Eur. J. Biochem. 1993;215:213-219.
Not in our library10.1111/j.1432-1033.1993.tb18025.x
- 17.
Pinchuk I., Shoval H., Dotan Y., Lichtenberg D. Evaluation of antioxidants: Scope, limitations and relevance of assays. Chem. Phys. Lipids. 2012;165:638-647.
Not in our library10.1016/j.chemphyslip.2012.05.003
- 18.
Pompella A., Sies H., Wacker R., Brouns F., Grune T., Biesalski H.K., Frank J. The use of total antioxidant capacity as surrogate marker for food quality and its effect on health is to be discouraged. Nutrition. 2014;30:791-793.
Not in our library10.1016/j.nut.2013.12.002
- 19.
Sies H. Total antioxidant capacity: Appraisal of a concept. J. Nutr. 2007;137:1493-1495.
Not in our library10.1093/jn/137.6.1493
- 20.
Wayner D.D., Burton G.W., Ingold K.U., Locke S. Quantitative measurement of the total, peroxyl radical-trapping antioxidant capability of human blood plasma by controlled peroxidation. The important contribution made by plasma proteins. FEBS Lett. 1985;187:33-37.
Not in our library10.1016/0014-5793(85)81208-4
- 21.
Bartosz G. Non-enzymatic antioxidant capacity assays: Limitations of use in biomedicine. Free Radic. Res. 2010;44:711-720.
Not in our library10.3109/10715761003758114
- 22.
Lushchak V.I. Free radicals, reactive oxygen species, oxidative stress and its classification. Chem. Biol. Interact. 2014;224C:164-175.
Not in our library10.1016/j.cbi.2014.10.016
- 23.
Egea J., Fabregat I., Frapart Y.M., Ghezzi P., Görlach A., Kietzmann T., Kubaichuk K., Knaus U.G., Lopez M.G., Olaso-Gonzales G., et al. European contribution to the study of ROS: A summary of the findings and prospects for the future from the COST action BM1203 (EU-ROS). Redox. Biol. 2017;13:94-162.
Not in our library10.1016/j.redox.2017.05.007
- 24.
Jones D.P., Sies H. The redox code. Antioxid. Redox Signal. 2015;23:734-746.
Not in our library10.1089/ars.2015.6247
- 25.
Griffiths H.R., Møller L., Bartosz G., Bast A., Bertoni-Freddari C., Collins A., Cooke M., Coolen S., Haenen G., Hoberg A.-M., et al. Biomarkers. Mol. Aspects Med. 2002;23:101-208.
Not in our library10.1016/s0098-2997(02)00017-1
- 26.
Frijhoff J., Winyard P.G., Zarkovic N., Davies S.S., Stocker R., Cheng D., Knight A.R., Taylor E.L., Oettrich J., Ruskovska T., et al. Clinical relevance of biomarkers of oxidative stress. Antioxid. Redox Signal. 2015;23:1144-1170.
Not in our library10.1089/ars.2015.6317
- 27.
Lichtenberg D., Pinchuk I., Weber D. Oxidative stress, as assayed by a single test, cannot be used as a diagnostic tool. Biofactors. 2018;44:222-223.
Not in our library10.1002/biof.1420
- 28.
Ghezzi P., Ghiara V., Davies K., Sies H. Epistemological challenges of the oxidative stress theory of disease and the problem of biomarkers. Oxidative Stress: Eustress and Distress. 2020;13-27.
Not in our library
- 29.
Ghezzi P. Environmental risk factors and their footprints in vivo—A proposal for the classification of oxidative stress biomarkers. Redox Biol. 2020;34:101442.
Not in our library10.1016/j.redox.2020.101442
- 30.
Kagan V.E., Tyurina Y.Y., Sun W.Y., Vlasova I.I., Dar H., Tyurin V.A., Amoscato A.A., Mallampalli R., van der Wel P.C.A., He R.R., et al. Redox phospholipidomics of enzymatically generated oxygenated phospholipids as specific signals of programmed cell death. Free Radic. Biol. Med. 2020;147:231-241.
Not in our library10.1016/j.freeradbiomed.2019.12.028
- 31.
Liu X., Long M.J.C., Aye Y. Proteomics and beyond: Cell decision-making shaped by reactive electrophiles. Trends Biochem. Sci. 2019;44:75-89.
Not in our library10.1016/j.tibs.2018.09.014
- 32.
- 33.
- 34.
Liu K.H., Nellis M., Uppal K., Ma C., Tran V., Liang Y., Walker D.I., Jones D.P. Reference Standardization for quantification and harmonization of large-scale metabolomics. Anal. Chem. 2020;92:8836-8844.
Not in our library10.1021/acs.analchem.0c00338
- 35.
Pinchuk I., Weber D., Kochlik B., Stuetz W., Toussaint O., Debacq-Chainiaux F., Dolle M.E.T., Jansen E.H.J.M., Gonos E.S., Sikora E., et al. Gender- and age-dependencies of oxidative stress, as detected based on the steady state concentrations of different biomarkers in the MARK-AGE study. Redox Biol. 2019;24:101204.
Not in our library10.1016/j.redox.2019.101204
- 36.
Hayes J.D., Dinkova-Kostova A.T., Tew K.D. Oxidative stress in cancer. Cancer Cell. 2020;38:167-197.
Not in our library10.1016/j.ccell.2020.06.001
- 37.
Kim S.Y., Park C., Jang H.J., Kim B.O., Bae H.W., Chung I.Y., Kim E.S., Cho Y.-H. Antibacterial strategies inspired by the oxidative stress and response networks. J. Microbiol. 2019;57:203-212.
Not in our library10.1007/s12275-019-8711-9
- 38.
Sbodio J.I., Snyder S.H., Paul B.D. Redox mechanisms in neurodegeneration: From disease outcomes to therapeutic opportunities. Antioxid. Redox Signal. 2019;30:1450-1499.
Not in our library10.1089/ars.2017.7321
- 39.
Vassalle C., Maltinti M., Sabatino L. Targeting oxidative stress for disease prevention and therapy: Where do we stand, and where do we go from here. Molecules. 2020;25:2653.
Not in our library10.3390/molecules25112653
- 40.
Casas A.I., Dao V.T., Daiber A., Maghzal G.J., di Lisa F., Kaludercic N., Leach S., Cuadrado A., Jaquet V., Seredenina T., et al. Reactive oxygen-related diseases: Therapeutic targets and emerging clinical indications. Antioxid. Redox Signal. 2015;23:1171-1185.
Not in our library10.1089/ars.2015.6433
- 41.
Aschbacher K., Mason A.E., Sies H. Eustress, distress and oxidative stress: Promising pathways for mind-body medicine. Oxidative Stress: Eustress and Distress. 2020;583-617.
Not in our library
- 42.
Aschbacher K., O’Donovan A., Wolkowitz O.M., Dhabhar F.S., Su Y., Epel E. Good stress, bad stress and oxidative stress: Insights from anticipatory cortisol reactivity. Psychoneuroendocrinology. 2013;38:1698-1708.
Not in our library10.1016/j.psyneuen.2013.02.004
- 43.
Siegrist J., Sies H. Disturbed redox homeostasis in oxidative stress: A molecular link from chronic psychosocial work stress to coronary heart disease? Circ. Res. 2017;121:103-105.
Not in our library10.1161/circresaha.117.311182
- 44.
Dennis K.K., Go Y.M., Jones D.P. Redox systems biology of nutrition and oxidative stress. J. Nutr. 2020;149:553-565.
Not in our library10.1093/jn/nxy306
Cited by papers we hold 7
- Phytochemical study and biological activities of Teucrium mideltense (Batt.) Humbert. · 2024Not checked
- The emerging role of oxidative stress in inflammatory bowel disease · 2024No notice
- Reactive oxygen species, toxicity, oxidative stress, and antioxidants: chronic diseases and aging · 2023No notice
- Oxidative Stress in Depression: The Link with the Stress Response, Neuroinflammation, Serotonin, Neurogenesis and Synaptic Plasticity · 2023No notice
- Lipid peroxidation in osteoarthritis: focusing on 4-hydroxynonenal, malondialdehyde, and ferroptosis · 2023No notice
- Revisiting the Oxidation of Flavonoids: Loss, Conservation or Enhancement of Their Antioxidant Properties · 2022No notice
- Magnetic field effects in biology from the perspective of the radical pair mechanism · 2022No notice
Reads
Read by people on this page
None yet.
Checked or read by AI through naulon
None yet.
A person counts once a day per paper. We keep no cookie and no address: a reader is a hash that changes every day. Any month under five reads shows no number.
Are you an author?
Is this your paper?
Claim it to add your note and be paid when agents cite it. Free.