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Oxidative damage to mitochondrial DNA shows marked age-dependent increases in human brain
Abstract
A major theory of aging is that oxidative damage may accumulate in DNA and contribute to physiological changes associated with aging. We examined age-related accumulation of oxidative damage to both nuclear DNA (nDNA) and mitochondrial DNA (mtDNA) in human brain tissue. We measured the oxidized nucleoside, 8-hydroxy-2'-deoxyguanosine (OH8dG), in DNA isolated from 3 regions of cerebral cortex and cerebellum from 10 normal humans aged 42 to 97 years. The amount of OH8dG, expressed as a ratio of the amount of deoxyguanosine (dG) or as fmol/micrograms of DNA, increased progressively with normal aging in both nDNA and mtDNA; however, the rate of increase with age was much greater in mtDNA. There was a significant 10-fold increase in the amount of OH8dG in mtDNA as compared with nDNA in the entire group of samples, and a 15-fold significant increase in patients older than 70 years. These results show for the first time that there is a progressive age-related accumulation in oxidative damage to DNA in human brain, and that the mtDNA is preferentially affected. It is possible that such damage may contribute to age-dependent increases in incidence of neurodegenerative diseases.
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“Oxidation of DNA and RNA produced by ROS also occurs in AD [50,51,52,53].”
From Role of Oxidative Damage in Alzheimer’s Disease and Neurodegeneration: From Pathogenic Mechanisms to Biomarker Discovery (2021) · cites this paper as [50]
In the citing paper
“It is demonstrated that there is a progressive age-related accumulation of oxidative damage to DNA in the human brain and that mtDNA is preferentially affected. The increased amount of 8-OHdG in mtDNA and nuclear DNA is demonstrated in the aging human brain and in AD [50,51,64].”
From Role of Oxidative Damage in Alzheimer’s Disease and Neurodegeneration: From Pathogenic Mechanisms to Biomarker Discovery (2021) · cites this paper as [50]
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“A number of laboratories studied age-related changes in 8-hydroxy-2’-deoxyguanosine (8-OHdG) as a marker of oxidative DNA damage in a variety of tissues, and it was suggested that this age-related increase in oxidative DNA damage is generally due to continuous exposure to oxidants during the aging process (Ames, 1989;…”
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“The reasons might lie in three points: (1) lack of protective histones and proximity ROS originating from mitochondria [23]; (2) intact DNA damage repair in mitochondria and (3) accumulating of MWCNTs in mitochondria rather in nucleus.”
BackgroundMultifaceted mitochondrial as a novel therapeutic target in dry eye: insights and interventions
Ouyang, W., Yan, D., Hu, J., & Liu, Z. (2024) · Cell Death Discovery · doi:10.1038/s41420-024-02159-0 · Cited by 25
Consideration of nutrient levels in studies of cognitive decline
Barnes, J. L., Tian, M., Edens, N. K., & Morris, M. C. (2014) · Nutrition Reviews · doi:10.1111/nure.12144 · Cited by 24
Age-related alteration of poly(ADP-ribose) polymerase activity in different parts of the brain.
Strosznajder, J. B., Jęśko, H. M., & Strosznajder, R. P. (2000) · Acta Biochimica Polonica · doi:10.18388/abp.2000_4012 · Cited by 24
“It is possible that higher radical oxygen species (ROS) formation and DNA damage observed by Mecocci et al. (1993), Ashok et al. (1998), Lu et al. (1999), Edris et al. (1994) during aging may be responsible for this activation of PARP in old adult animals.”
BackgroundFree Radicals and Mitochondria Dysfunction in Excitotoxicity and Neurodegenerative Disease
Dykens, J. A. (1999) · Humana Press eBooks · doi:10.1007/978-1-4612-1602-5_3 · Cited by 24
Mitochondrial diseases and aging
Papa, S., Scacco, S., Schliebs, M., Trappe, J., & Seibel, P. (1996) · Molecular Aspects of Medicine · doi:10.1016/s0098-2997(96)00013-1 · Cited by 24
Deleterious network hypothesis of Alzheimer's disease
Ying, W. (1996) · Medical Hypotheses · doi:10.1016/s0306-9877(96)90021-3 · Cited by 21
Tiwari, M. K., & Mishra, P. C. (2013) · Journal of Molecular Modeling · doi:10.1007/s00894-013-2023-5 · Cited by 22
Beal, M. F. (2005) · Nature Medicine · doi:10.1038/nm0605-598 · Cited by 22
DNA versus RNA oxidation in Parkinson’s disease: Which is more important?
Gmitterová, K., Gawinecka, J., Heinemann, U., Valkovič, P., & Zerr, I. (2017) · Neuroscience Letters · doi:10.1016/j.neulet.2017.09.048 · Cited by 22
Expression profile and mitochondrial colocalization of Tdp1 in peripheral human tissues
Fam, H. K., Chowdhury, M. K., Walton, C., Choi, K., Boerkoel, C. F., & Hendson, G. (2013) · Journal of Molecular Histology · doi:10.1007/s10735-013-9496-5 · Cited by 21
Jeng, W., & Wells, P. G. (2010) · ACS Chemical Neuroscience · doi:10.1021/cn900022w · Cited by 21
Shehata, N. I., Abdelgawad, H. M., Mawsouf, M. N., & Shaheen, A. A. (2012) · Biogerontology · doi:10.1007/s10522-012-9400-9 · Cited by 21
“accumulation of oxidative damage to mtDNA (Mecocci et al. 1993).”
BackgroundMitochondrial DNA Damage Does Not Determine C. elegans Lifespan
Ng, L. F., Ng, L. T., van Breugel, M., Halliwell, B. B., & Gruber, J. (2019) · Frontiers in Genetics · doi:10.3389/fgene.2019.00311 · Cited by 22
Shen, S., Cooley, D. M., Glickman, L. T., Glickman, N. W., & Waters, D. J. (2001) · Mutation research. Fundamental and molecular mechanisms of mutagenesis · doi:10.1016/s0027-5107(01)00179-8 · Cited by 21
Soerensen, M., Gredilla, R., Mueller-Ohldach, M., Werner, A., Bohr, V. A., Osiewacz, H. D., & Stevnsner, T. (2009) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2009.05.003 · Cited by 21
“8oxodG has been found to accumulate in mtDNA with age in both mice, rats and humans (Richter et al. 1988;Mecocci et al. 1993;Takasawa et al. 1993; Lindahl 1993;Hayakawa et al. 1993;Short et al. 2005).”
BackgroundOxidative Alterations in Neurodegenerative Diseases
Markesbery, W. R., Montine, T. J., & Lovell, M. A. (2001) · Humana Press eBooks · doi:10.1007/978-1-59259-106-0_2 · Cited by 27
“Mecocci et al. (1993) reported an increase in 8-OHdG in nuclear and mitochondrial brain fractions in aging.”
BackgroundPotential of Neuroprotective Therapy in Parkinsonʼs Disease
Mizuno, Y., Mori, H., & Kondo, T. (1994) · CNS Drugs · doi:10.2165/00023210-199401010-00005 · Cited by 21
Reciprocal interactions between mtDNA and lifespan control in budding yeast
Garcia, E. J., de Jonge, J. J., Liao, P., Stivison, E., Sing, C. N., Higuchi‐Sanabria, R., Boldogh, I. R., & Pon, L. A. (2019) · Molecular Biology of the Cell · doi:10.1091/mbc.e18-06-0356 · Cited by 21
“…there is an age-associated increase in oxidative damage and mutations in mtDNA and a decrease in mitochondrial respiration in humans, mice, and mammalian cells (MullerHocker, 1989, 1990; Muller-Hocker et al., 1992; Trounce et al., 1989; Mecocci et al., 1993; Melov et al., 1995, 1997, 1999).”
BackgroundATFS-1 counteracts mitochondrial DNA damage by promoting repair over transcription
Dai, C.-Y., Ng, C. C., Hung, G. C. C., Kirmes, I., Hughes, L. A., Du, Y., Brosnan, C. A., Ahier, A., Hahn, A., Haynes, C. M., et al. (2023) · Nature Cell Biology · doi:10.1038/s41556-023-01192-y · Cited by 20
Gündüztepe, Y., Bukan, N. C., Zorlu, E., Karaman, Y., Topkan, T. A., Gürbüz, N., Neşeli̇oğlu, S., & Erel, Ö. (2020) · Journal of Clinical Neuroscience · doi:10.1016/j.jocn.2019.12.026 · Cited by 19
Metadata
- Authors
- Mecocci, P., MacGarvey, U., Kaufman, A. E., Koontz, D., Shoffner, J. M., Wallace, D. C., & Beal, M. F.
- Affiliations
- Harvard University (US)
- Emory University (US)
- Corresponding author
- Beal, M. Flint
- Venue
- Annals of Neurology
- Publisher
- Wiley
- Published
- 1993-10
- Volume
- 34
- Issue
- 4
- Pages
- 609-616
- ISSN
- 0364-5134 (ISSN-L)
- 1531-8249
- OpenAlex
- W2130753450
- Cited by
- 757
- References
- 50
- Citations by year
- 2026: 5 · 2025: 7 · 2024: 12 · 2023: 12 · 2022: 15 · 2021: 18 · 2020: 19 · 2019: 22 · 2018: 17 · 2017: 16 · 2016: 19 · 2015: 18 · 2014: 24 · 2013: 29 · 2012: 22
- FWCI
- 7.34
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Annals of Neurology (publishedVersion)
- PubMed (publishedVersion)
- Funders
- U.S. Public Health Service (16367)
- National Institute on Aging (IP50 AG05134)
- National Institute of Neurological Disorders and Stroke (NS-21328, R01NS021328)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Mitochondrial Function and Pathology
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Aging › Genetics, Aging, and Longevity in Model Organisms
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › DNA Repair Mechanisms
- Keywords
- oxidative DNA damage, mitochondrial DNA, 8-hydroxy-2'-deoxyguanosine, brain aging, cerebral cortex, cerebellum, nuclear DNA, age-related accumulation, neurodegenerative diseases
- MeSH terms
- 8-Hydroxy-2'-Deoxyguanosine, Adult, Aged, Aged, 80 and over, Aging, Brain, Cell Nucleus, Deoxyguanosine, DNA, DNA, Mitochondrial, Female, Humans, Male, Middle Aged, Oxidation-Reduction
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