Hostname: page-component-78c5997874-s2hrs Total loading time: 0 Render date: 2024-11-09T15:08:22.610Z Has data issue: false hasContentIssue false

Methods to detect DNA damage by free radicals: relation to exercise

Published online by Cambridge University Press:  12 June 2007

Henrik E. Poulsen*
Affiliation:
Department of Clinical Pharmacology, Rigshospitalet, University Hospital Copenhagen, Denmark
Allan Weimann
Affiliation:
Department of Clinical Pharmacology, Rigshospitalet, University Hospital Copenhagen, Denmark
Steffen Loft
Affiliation:
Department of Public Health, Panum Institute, Health Science Faculty, Copenhagen University, Denmark
*
*Corresponding Author: Professor Henrik E. Poulsen, fax +45 3545 2745, email [email protected]
Rights & Permissions [Opens in a new window]

Abstract

Core share and HTML view are not available for this content. However, as you have access to this content, a full PDF is available via the ‘Save PDF’ action button.

Epidemiological investigations repeatedly show decreased morbidity from regular exercise compared with sedentary life. A large number of investigations have demonstrated increased oxidation of important cellular macromolecules, whereas other investigators have found no effects or even signs of lowering of oxidation of macromolecules. In particular, extreme and long-duration strenuous exercise appears to lead to deleterious oxidation of cellular macromolecules. The oxidation of DNA is important because the oxidative modifications of DNA bases, particularly the 8-hydroxylation of guanine, are mutagenic and have been implicated in a variety of diseases such as ageing and cancer. The methodologies for further investigation of the relationship between DNA oxidation and exercise are available. The preferred methods rely on HPLC or GC-mass spectrometry; whereas the theoretically-attractive liquid chromatography- tandem mass spectrometry is being developed. Caution should be taken to avoid artifacts because of the six orders of magnitude of difference between oxidized and non-oxidized DNA bases in tissues. The methods can be used to estimate tissue levels, i.e. a local concentration of oxidized DNA, or to estimate the rate of body DNA oxidation by the urinary output of repair products, the latter being a method that is independent of repair. During exercise there appears to be a shifting of dietary-dependent antioxidant, e.g. vitamin C and vitamin E, from muscle to plasma, and an increased oxidation in plasma of these antioxidants. Supplementation trials with antioxidants have not been able to increase exercise performance; however, optimum nutrition with antioxidants and possibly supplementation, could be important in the prevention of diseases in the long term. The pattern from these observations appears to be quite consistent; immediately after exercise, regardless of how intense, there do not appear to be any signs of oxidative damage to DNA. Acute or prolonged moderate exercise does not produce signs of oxidative DNA damage and might even be associated with lowering of the levels of oxidation of tissue DNA; however, after long-duration and intense exercise an increase in oxidative DNA modifications is apparent. We suggest as a hypothesis that the relationship between exercise and health is U-shaped. This hypothesis needs to be tested in detail in order to establish the maximum beneficial exercise level with regard to oxidative DNA modification, and also the level that could be deleterious and might even increase the risk for cancer and other diseases.

Type
Meeting Report
Copyright
The Nutrition Society

References

Adelman, R, Saul, RL & Ames, BN (1988) Oxidative damage to DNA: Relation to species metabolic rate and life span. Proceedings of the National Academy of Sciences USA 85, 27062708.CrossRefGoogle ScholarPubMed
Ames, BN & Saul, RL (1986) Oxidative DNA damage as related to cancer and ageing. In. Principles and Mechanism of Action,p. 11 New York: Alan R Liss Inc.Google Scholar
Ames, BN & Shigenaga, MK (1992) Oxidants are a major contributor to aging. Annals of the New York Academy of Sciences 663, 8596.CrossRefGoogle Scholar
Ames, BN, Shigenaga, MK & Hagen, TM (1993) Oxidants, antioxidants, and the degenerative diseases of aging. Proceedings of the National Academy of Sciences USA 90, 79157922.CrossRefGoogle ScholarPubMed
Bessho, T, Tano, K, Kasai, H, Ohtsuka, E & Nishimura, S (1993) Evidence for two DNA repair enzymes for 8-hydroxyguanine (7,8-dihydro-guanine) in human cells. Journal of Biological Chemistry 268, 1941619421.CrossRefGoogle Scholar
Bianchini, F, Donato, F, Faure, H, Ravanat, JL, Hall, J. & Cadet, J (1998) Urinary excretion of 5-(hydroxymethyl) uracil in healthy volunteers: effect of active and passive tobacco smoke. International Journal of Cancer 77, 4046.3.0.CO;2-#>CrossRefGoogle ScholarPubMed
CadetJ,. Incardona MF J,. Incardona MF, Odin, F, Molko, D, Mouret, JF, Polverelli, M, Faure, H, Ducros, V, Tripier, M & Favier, A (1993) Measurement of oxidative base damage to DNA by using HPLC-32P-postlabelling and GC/MS-selective ion monitoring assays. In IARC Scientific Publications, pp. 271276.Lyon, France: IARC.Google Scholar
Cadet, J, Ravanat, JL, Buchko, GW, Yeo, HC & Ames, BN (1994) Singlet oxygen DNA damage: chromatographic and mass spectrometric analysis of damage products. Methods in Enzymology 234, 7988.CrossRefGoogle ScholarPubMed
Chance, B, Sies, H & Boveris, A (1979) Hydroperoxide metabolism in mammalian organs. Physiology Review 59, 527605.CrossRefGoogle ScholarPubMed
Child, RB, Wilkinson, DM, Fallowfield, JL & Donnelly, AE (1998) Elevated serum antioxidant capacity and plasma malondialdehyde concentration in response to a simulated half-marathon run. Medicine and Science in Sports and Exercise 30, 16031607.CrossRefGoogle ScholarPubMed
Collins, A, Cadet, J, Epe, B & Gedik, C (1997a) Problems in the measurement of 8-oxoguanine in human DNA. Report of a workshop, DNA oxidation, held in Aberdeen, UK, 19–21 January, 1997. Carcinogenesis 18, 18331836.CrossRefGoogle ScholarPubMed
Collins, AR, Ai-guo, M & Duthie, SJ (1995) The kinetics of repair of oxidative DNA damage (strand breaks and oxidised pyrimidines) in human cells. Mutation Research 336, 6977.CrossRefGoogle ScholarPubMed
Collins, AR, Dobson, VL, Dusinska, M, Kennedy, G. & Stetina, R (1997b) The comet assay: what can it really tell us? Mutation Research 375, 183193.CrossRefGoogle ScholarPubMed
Collins, AR, Dusinska, M, Gedik, CM & Stetina, R (1996) Oxidative damage to DNA: do we have a reliable biomarker? Environmental Health Perspectives 104, Suppl. 3, 465469.CrossRefGoogle ScholarPubMed
Deng, XS, Tuo, J, Poulsen, HE & Loft, S (1997) 2-Nitropropane-induced DNA damage in rat bone marrow. Mutation Research 391, 165169.CrossRefGoogle ScholarPubMed
Deskur, E, Przywarska, I, Dylewicz, P, Szczesniak, L, Rychlewski, T, Wilk, M & Wysocki, H (1998) Exercise induced increase in hydrogen peroxide plasma levels is diminished by endurance training after myocardial infarction. International Journal of Cardiology 67, 219224.CrossRefGoogle ScholarPubMed
Dizdaroglu, M (1985) Formation of an 8-hydroxyguanine moiety in deoxyribonucleic acid on gamma-irradiation in aqueous solution. Biochemistry 24, 44764481.CrossRefGoogle ScholarPubMed
Dizdaroglu, M (1991) Chemical determination of free radical-induced damage to DNA. Free Radicals in Biology and Medicine 10, 225242.CrossRefGoogle ScholarPubMed
Dizdaroglu, M (1992) Oxidative damage to DNA in mammalian chromatin. Mutation Research 275, 331342.CrossRefGoogle ScholarPubMed
Dizdaroglu, M (1993) Chemistry of free radical damage to DNA and nucleoproteins. In DNA and Free Radicals, pp. 1939[Halliwell, B, editor]. Chichester, West Sussex: Ellis Horwood Ltd.Google ScholarPubMed
Dizdaroglu, M (1994) Chemical determination of oxidative DNA damage by gas chromatography-mass spectrometry. Methods in Enzymology 234, 316.CrossRefGoogle ScholarPubMed
Dizdaroglu, M & Bergtold, DS (1986) Characterization of free radical-induced base damage in DNA at biological relevant levels. Analytical Biochemistry 156, 182188.CrossRefGoogle ScholarPubMed
Epe, B (1995) DNA damage profiles induced by oxidizing agents. Reviews in Physiology, Biochemistry and Pharmacology 127, 223249.CrossRefGoogle Scholar
Epe, B & Hegler, J (1994) Oxidative DNA damage: endonuclease fingerprinting. Methods in Enzymology 234, 122131.CrossRefGoogle ScholarPubMed
Erikssen, G, Liestøl, K, Bjørnholt, E, Thaulow, E, Sandvik, L, Erikssen, J & Aach, RD (1998) Changes in physical fitness and changes in mortality. Lancet 352, 759762.CrossRefGoogle ScholarPubMed
Esterbauer, H, Gebicki, J, Puhl, H & Jurgens, G (1992) The role of lipid peroxidation and antioxidants in oxidative modification of LDL. Free Radicals in Biology and Medicine 13, 341390.CrossRefGoogle ScholarPubMed
Faure, H, Incardona, MF, Boujet, C, Cadet, J, Ducros, V & Favier, A (1993) Gas chromatographic-mass spectrometric determination of 5-hydroxymethyluracil in human urine by stable isotope dilution. Journal of Chromatography 616, 17.CrossRefGoogle ScholarPubMed
Faure, H, MousseauM,. Cadet J M,. Cadet J, Guimier, C, Tripier, M, Hida, H & Favier, A (1998) Urine 8-oxo-7,8-dihydro-2-deoxyguanosine vs. 5-(hydroxymethyl) uracil as DNA oxidation marker in adriamycin-treated patients. Free Radical Research 28, 377382.CrossRefGoogle ScholarPubMed
Goldfarb, AH (1993) Antioxidants: role of supplementation to prevent exercise-induced oxidative stress. Medicine and Science in Sports and Exercise 25, 232236.CrossRefGoogle ScholarPubMed
Halliwell, B (1994) Free radicals, antioxidants, and human disease: curiosity, cause or consequence. Lancet 344, 721724.CrossRefGoogle ScholarPubMed
Haring, M, Rudiger, H, Demple, B, Boiteux, S & Epe, B (1994) Recognition of oxidized abasic sites by repair endonucleases. Nucleic Acids Research 22, 20102015.CrossRefGoogle ScholarPubMed
Hartmann, A, Niess, AM, Grunert-Fuchs, M, Poch, B. & Speit, G (1995) Vitamin E prevents exercise-induced DNA damage. Mutation Research 346, 195202.Google ScholarPubMed
Hartmann, A, Pfuhler, S, Dennog, C, Germadnik, D, Pilger, A & Speit, G (1998) Exercise-induced DNA effects in human leukocytes are not accompanied by increased formation of 8-hydroxy-2'-deoxyguanosine or induction of micronuclei. Free Radicals in Biology and Medicine 24, 245251.CrossRefGoogle ScholarPubMed
Hofer, T & Moller, L (1998) Reduction of oxidation during the preparation of DNA and analysis of 8-hydroxy-2'-deoxyguanosine. Chemical Research in Toxicology 11, 882887.CrossRefGoogle Scholar
Inoue, T, Zhouseng, M, Sumikawa, K, Adachi, K & Okochi, T (1998) Effect of physical exercise on the content of 8-hydroxydeoxyguanosine in nuclear DNA prepared from human lymphocytes. Japanese Journal of Cancer Research 84, 725750.Google Scholar
Kaikkonen, J, Kosonen, L, Nyyssonen, K, Porkkala-Sarataho, E, Salonen, R, Korpela, H & Salonen, JT (1998) Effect of combined coenzyme Q10 and D-alpha-tocopheryl acetate supplementation on exercise-induced lipid peroxidation and muscular damage: a placebo-controlled double-blind study in marathon runners. Free Radical Research 29, 8592.CrossRefGoogle Scholar
Kanter, M (1998) Free radicals, exercise and antioxidant supplementation. Proceedings of the Nutrition Society 57, 913.CrossRefGoogle ScholarPubMed
Kasai, H (1997) Analysis of a form of oxidative DNA damage, 8-hydroxy-2'-deoxyguanosine, as a marker of cellular oxidative stress during carcinogenesis. Mutation Research 387, 147163.CrossRefGoogle ScholarPubMed
Kasai, H & Nishimura, S (1984) Hydroxylation of deoxyguanosine at the C-8 position by ascorbic acid and other reducing agents. Nucleic Acids Research 12, 21372145.CrossRefGoogle ScholarPubMed
Kiningham, RB (1998) Physical activity and the primary prevention of cancer. Primary Care 25, 515536.CrossRefGoogle ScholarPubMed
Lee, IM, Paffenbarger, RS & Hennekens, CH (1997) Physical activity, physical fitness and longevity. Aging 9, 211.Google ScholarPubMed
Loft, S, Larsen, PN, Rasmussen, A, Fischer-Nielsen, A, Bondesen, S, Kirkegaard, P, Rasmussen, LS, Ejlersen, E, Tornoe, K, Bergholdt, R & Poulsen, HE (1995) Oxidative DNA damage after transplantation of the liver and small intestine in pigs. Transplantation 59, 1620.CrossRefGoogle ScholarPubMed
Loft, S & Poulsen, HE (1996) Cancer risk and oxidative DNA damage in man. Journal of Molecular Medicine 74, 297–312.(Published erratum in Journal of Molecular Medicine (1997), 75, 6768).CrossRefGoogle ScholarPubMed
Loft, S & Poulsen, HE (1998) Markers of oxidative damage to DNA: antioxidants and molecular damage. Methods in Enzymology 300, 166184.CrossRefGoogle Scholar
Loft, S, Vistisen, K, Ewertz, M, Tjonneland, A, Overvad, K & Poulsen;, HE (1992) Oxidative DNA damage estimated by 8-hydroxydeoxyguanosine excretion in humans: influence of smoking, gender and body mass index. Carcinogenesis 13, 22412247.CrossRefGoogle ScholarPubMed
Lovlin, R, Cottle, W, Pyke, I, Kavanagh, M & Belcastro, AN (1987) Are indices of free radical damage related to exercise intensity. European Journal of Applied Physiology and Occupational Physiology 56, 313316.CrossRefGoogle ScholarPubMed
Lunec, J (1999) ESCODD: European Standards Committee on Oxidative DNA Damage. Free Radical Research(In the Press).Google Scholar
Mecocci, P, Fano, G, Fulle, S, MacGarvey, U, Shinobu, L, Polidori, M, Cherubini, A, Vecchiet, J, Senin, U & Beal, MF (1999) Age-dependent increases in oxidative damage to DNA, lipids, and proteins in human skeletal muscle. Free Radicals in Biology and Medicine 26, 303308.CrossRefGoogle ScholarPubMed
Moller, L & Hofer, T (1997) [32P]ATP mediates formation of 8-hydroxy-2‘-deoxyguanosine from 2’-deoxyguanosine, a possible problem in the 32P-postlabelling assay. Carcinogenesis 18, 24152419.CrossRefGoogle Scholar
Moller, L, Zeisig, M & Vodicka, P (1993) Optimization of an HPLC method for analyses of 32P-postlabelled DNA adducts. Carcinogenesis 14, 13431348.CrossRefGoogle Scholar
Nielsen, HB, Hanel, B, Loft, S, Poulsen, HE, Pedersen, BK, Diamant, M, Vistisen, K & Secher, NH (1995) Restricted pulmonary diffusion capacity after exercise is not an ARDS-like injury. Journal of Sports Sciences 13, 109113.CrossRefGoogle Scholar
Niess, AM, Baumann, P, Roecker, K, Mayer, F & Dickhuth, HH (1998) Effects of intensive endurance exercise on DNA damage in leucocytes. Journal of Sports Medicine and Physical Fitness 38, 111115.Google ScholarPubMed
Niess, AM, Hartmann, A, Grunert-Fuchs, M, Poch, B. & Speit, G (1996) DNA damage after exhaustive treadmill running in trained and untrained men. International Journal of Sports Medicine 17, 397403.CrossRefGoogle ScholarPubMed
Okamura, K, Doi, T, Hamada, K, Sakurai, M, Yoshioka, Y, Mitsuzono, R, Migita, T, Sumida, S & Sugawa, KY (1997) Effect of repeated exercise on urinary 8-hydroxy-deoxyguanosine excretion in humans. Free Radical Research 26, 507514.CrossRefGoogle ScholarPubMed
Oliveria, SA & Christos, PJ (1997) The epidemiology of physical activity and cancer. Annals of the New York Academy of Sciences 833, 7990.CrossRefGoogle ScholarPubMed
Packer, L (1997) Oxidants, antioxidant nutrients and the athlete. Journal of Sports Sciences 15, 353363.CrossRefGoogle ScholarPubMed
Paffenberger, RS, Hyde, RT, Wing, AL, Lee, IM, Jung, DL & Kampert, JB (1993) The association of changes in physical-activity level and other lifestyle characteristics with mortality among men. New England Journal of Medicine 328, 538545.CrossRefGoogle Scholar
Palmer, HJ & Paulson, KE (1997) Reactive oxygen species and antioxidants in signal transduction and gene expression. Nutrition Reviews 55, 353361.CrossRefGoogle ScholarPubMed
Pedersen, BK, Rohde, T & Zacho, M (1996) Immunity in athletes. Journal of Sports Medicine and Physical Fitness 36, 236245.Google ScholarPubMed
Pflaum, M, Kielbassa, C, Garmyn, M & Epe, B (1998) Oxidative DNA damage induced by visible light in mammalian cells: extent, inhibition by antioxidants and genotoxic effects. Mutation Research 408, 137146.CrossRefGoogle ScholarPubMed
Pflaum, M, Will, O & Epe, B (1997) Determination of steady-state levels of oxidative DNA base modifications in mammalian cells by means of repair endonucleases. Carcinogenesis 18, 22252231.CrossRefGoogle ScholarPubMed
Pilger, A, Germadnik, D, Formanek, D, Zwick, H, Winkler, N & Rudiger, HW (1997) Habitual long-distance running does not enhance urinary excretion of 8-hydroxydeoxyguanosine. European Journal of Applied Physiology and Occupational Physiology 75, 467469.CrossRefGoogle Scholar
Poulsen, HE, Loft, S, Prieme, H, Vistisen, K, Lykkesfeldt, J, Nyyssonen, K & Salonen, JT (1999a) Oxidative DNA damage in vivo: Relationship to age, plasma antioxidants, drug metabolism, glutathione-S-transferase activity and urinary creatinine excretion. Free Radical Research(In the Press).Google Scholar
Poulsen, HE, Loft, S & Vistisen, K (1996) Extreme exercise and oxidative DNA modification. Journal of Sports Sciences 14, 343346.Google Scholar
Poulsen, HE, Prieme, H & Loft, S (1998a) Role of oxidative DNA damage in cancer initiation and promotion. European Journal of Cancer Prevention 7, 916.Google ScholarPubMed
Poulsen, HE, ., Weimann A & Loft, S (1999b) Urinary measurement of 8-oxodG (8-oxo-2'-deoxyguanosine). In Handbook of Clinical Analysis: In Vivo Damage to Biomolecules.[Lunec, J, editor]. London: John Wiley and Sons Ltd (In the Press).Google Scholar
Poulsen, HE, Weimann, A, Salonen, JT, Nyyssonen, K, Loft, S, Cadet, J, Douki, T & Ravanat, JL (1998b) Does vitamin C have a pro-oxidant effect? Nature 395, 231232.CrossRefGoogle ScholarPubMed
Prieme, H, Loft, S, Cutler, RG & Poulsen, HE (1996) Measurement of oxidative DNA injury in humans: evaluation of a commercially available ELISA assay. In Natural Antioxidants and Food Quality in Atherosclerosis and Cancer Prevention, pp. 7882 [Kumpulainen, JT, editor]. London: The Royal Society of Chemistry.Google Scholar
Ravanat, JL, Duretz, B, Guiller, A, Douki, T & Cadet, J (1998) Isotope dilution high-performance liquid chromatography–electrospray tandem mass spectrometry assay for the measurement of 8-oxo-7,8-dihydro-2'-deoxyguanosine in biological samples. Journal of Chromatography 715, 349356.CrossRefGoogle ScholarPubMed
Ravanat, JL, Turesky, RJ, Gremaud, E, Trudel, LJ. & Stader, RH (1995) Determination of 8-oxoguanine in DNA by gas chromatography-mass spectrometry and HPLC-electrochemical detection: overestimation of the background level of the oxidized base by the gas chromatography-mass spectrometry assay. Chemical Research in Toxicology 8, 10391045.CrossRefGoogle ScholarPubMed
Retèl, J, Hoebee, B, Braun, JEF, Lutgerink, JT, van den, Akker E, Wanamarta, AH, Joneje, H & Lafleur, MVM (1993) Mutational specificity of oxidative DNA damage. Mutation Research 299, 165182.CrossRefGoogle ScholarPubMed
Ross, GM, McMillan, TJ, Wilcox, P & Collins, AR (1995) The single cell microgel electrophoresis assay (comet assay): technical aspects and applications. Report on the 5th LH Gray Trust Workshop, Institute of Cancer Research, 1994. Mutation Research 337, 5760.CrossRefGoogle Scholar
Sadekova, S, Lehnert, S & Chow, TY (1997) Induction of PBP74/mortalin/Grp75, a member of the hsp70 family, by low doses of ionizing radiation: a possible role in induced radioresistance. International Journal of Radiation Biology 72, 653660.CrossRefGoogle ScholarPubMed
Schuler, D, Otteneder, M, Sagelsdorff, P, Eder, E, Gupta, RC & Lutz, WK (1997) Comparative analysis of 8-oxo-2-deoxyguanosine in DNA by 32P- and 33P-postlabelling and electrochemical detection. Carcinogenesis 18, 23672371.CrossRefGoogle ScholarPubMed
Shigenaga, MK, Gimeno, CJ & Ames, BN (1989) Urinary 8-hydroxy-2-deoxyguanosine as a biological marker of in vivo oxidative DNA damage. Proceedings of the National Academy of Sciences USA 86, 96979701.CrossRefGoogle ScholarPubMed
Sumida, S, Doi, T, Sakurai, M, Yoshioka, Y & Okamura, K (1997) Effect of a single bout of exercise and beta-carotene supplementation on the urinary excretion of 8-hydroxy-deoxyguanosine in humans. Free Radical Research 27, 607618.CrossRefGoogle ScholarPubMed
Tuo, J, Loft, S, Thomsen, MS & Poulsen, HE (1996) Ex vivo time-dependent cell DNA-degradation shown by single cell gel electrophoresis. Pharmacology and Toxicology 78, 5557.CrossRefGoogle ScholarPubMed
Viguie, CA, Frei, B, Shigenaga, MK, Ames, BN, Packer, L & Brooks, GA (1993) Antioxidant status and indexes of oxidative stress during consecutive days of exercise. Journal of Applied Physiology 75, 566572.CrossRefGoogle ScholarPubMed
Wiseman, H & Halliwell, B (1996) Damage to DNA by reactive oxygen and nitrogen species: role in inflammatory disease and progression to cancer. Biochemical Journal 313, 1729.CrossRefGoogle ScholarPubMed
Witt, EH, Reznick, AZ, Viguie, CA, Starke-Reed, P. & Packer, L (1992) Exercise, oxidative damage and effects of antioxidant manipulation. Journal of Nutrition 122, 766773.CrossRefGoogle ScholarPubMed
Zeisig, M & Moller, L (1997) 32P-Postlabelling high-performance liquid chromatographic improvements to characterize DNA adduct stereoisomers from benzo[a]pyrene and benzo[c]- phenanthrene, and to separate DNA adducts from 7,12-dimethylbenz[a]anthracene. Journal of Chromatography 691, 341350.CrossRefGoogle Scholar