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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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Liu, P. K., Robertson, C. S., & Valadka, A. B. (2002) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2002.tb04071.x · Cited by 48
Zhang, C., Nestorova, G. G., Rissman, R. A., & Feng, J. (2013) · Electrophoresis · doi:10.1002/elps.201300036 · Cited by 47
Long-term cadmium exposure accelerates age-related mitochondrial changes in renal epithelial cells
Takaki, A., Jimi, S., Segawa, M., Hisano, S., Takebayashi, S., & Iwasaki, H. (2004) · Toxicology · doi:10.1016/j.tox.2004.06.005 · Cited by 47
Neuropathology of synuclein aggregates
Duda, J. E., Lee, V. M. ‐., & Trojanowski, J. Q. (2000) · Journal of Neuroscience Research · doi:10.1002/1097-4547(20000715)61:2 · Cited by 263
Robinson, R. A. S., Gururaj Joshi, A., Huang, Q., Rukhsana Sultana, A., Baker, A. S., Cai, J., Pierce, W. M. J., Clair, D. K. S., Markesbery, W. R., & Butterfield, D. A. (2011) · PROTEOMICS · doi:10.1002/pmic.201000523 · Cited by 45
“…Butterfield1,4,6 1 Department of Chemistry, University of Kentucky, Lexington, KY, USA 2 Department of Pharmacology and Toxicology, School of Medicine, University of Louisville, Louisville, KY, USA 3 Department of Toxicology, University of Kentucky, Lexington, KY, USA 4 Sanders-Brown Center…”
BackgroundDNA induced folding/fibrillation of alpha-synuclein: new insights in Parkinson's disease
Hegde, M. L. (2009) · Frontiers in bioscience · doi:10.2741/3628 · Cited by 46
“The level of iron, which is significantly higher in the normal SN than in other regions owing to its binding affinity to neuromelanin, was further increased in the SN of PD further contributing to oxidative stress (41, 44-49).”
BackgroundMitochondrial electron transport chain activities and DNA deletions in regions of the rat brain
Filburn, C. R., Edris, W. A., Tamatani, M., Hogue, B. A., Kudryashova, I. V., & Hansford, R. G. (1996) · Mechanisms of Ageing and Development · doi:10.1016/0047-6374(96)01696-x · Cited by 46
Evidence against increased oxidative DNA-damage in Down syndrome
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Of Energy and Entropy: The Ineluctable Impact of Aging in Old Age Dementia
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“A progressive age-related accumulation of oxidative damage to DNA in the human brain and mitochondrial DNA have been found [75], suggesting that such damage may contribute to the age-dependent increase in the incidence of neurodegenerative diseases.”
BackgroundRole of Mitochondrial DNA Mutations in Disease and Aging
COTTRELL, D. A., Blakely, E. L., Borthwick, G. M., Johnson, M. A., Taylor, G. A., Brierley, E. J., Ince, P. G., & Turnbull, D. M. (2000) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2000.tb06647.x · Cited by 45
Oxidative Damage and Fragmentation of Mitochondrial DNA in Cellular Apoptosis
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“Compared with nuDNA, human mtDNA is more susceptible to oxidative damage in a variety of tissues including brain [62], since mitochondria generates the majority of energy for cells through oxidative phosphorylation, producing abundant ROS [63, 64] and lacks protection from histones, [65].”
BackgroundPetruski‐Ivleva, N., Kucharska‐Newton, A., Palta, P., Couper, D. J., Meyer, K. A., Graff, M., Haring, B., Sharrett, R. A., & HEISS, G. M. (2017) · Nutrients · doi:10.3390/nu9101134 · Cited by 45
Effects of Levocarnitine on Mitochondrial Antioxidant Systems and Oxidative Stress in Aged Rats
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8OHdG levels in brain do not indicate oxidative DNA damage in Alzheimer's disease
Koppele, J. M. T., Lucassen, P. J., Sakkee, A. N., Asten, J. G. V., Ravid, R., Swaab, D. F., & van Bezooijen, C. F. A. (1996) · Neurobiology of Aging · doi:10.1016/s0197-4580(96)00165-0 · Cited by 44
Morioka, N., Okatani, Y., & Wakatsuki, A. (1999) · Journal of Pineal Research · doi:10.1111/j.1600-079x.1999.tb00616.x · Cited by 44
Genetic Maternal Effects on HumanLife Span through the Inh eritance of Mitochondrial DNA
Korpelainen, H. (1999) · Human Heredity · doi:10.1159/000022871 · Cited by 43
Park, K. W., & Jin, B. K. (2008) · Journal of Neuroscience Research · doi:10.1002/jnr.21571 · Cited by 43
“Several studies have demonstrated that the brains of AD patients show evidence of oxidative stress, including oxidative modifications to proteins (Hensley et al., 1995), lipids (Palmer and Burns, 1994), and DNA (Mecocci et al., 1993).”
Kang, K., Yun, J.-W., & Lee, Y.-S. (2002) · Cancer Letters · doi:10.1016/s0304-3835(01)00821-7 · Cited by 43
Abdelkarim, D., Zhao, Y., Turner, M. P., Sivakolundu, D. K., Lu, H., & Bart Rypma, A. (2019) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2019.09.005 · Cited by 47
Lu, C., Ma, Y., Lin, J., Chuang, C., & Sung, F. (2006) · Environmental Research · doi:10.1016/j.envres.2006.08.009 · Cited by 43
“Age could influence the excretion of 8-OHdG in human tissues and in urine (Mecocci et al., 1993).”
BackgroundAliev, G., Palacios, H. H., Gasimov, E. K., Obrenovich, M. E., Morales, L., Leszek, J., Bragin, V., Herrera, A. S., & Gokhman, D. (2010) · Pharmaceuticals · doi:10.3390/ph3010158 · Cited by 43
“Studies demonstrate a decline in polyunsaturated fatty acids (PUFA) [21–23], increased levels of lipid peroxidation markers [19,21], as well as protein oxidation [24,25], DNA oxidation [26–28] and RNA oxidation [1,29–31] during AD.”
BackgroundAging and oxidative stress in progressive supranuclear palsy
Aoyama, K., Matsubara, K., & Kobayashi, S. (2006) · European Journal of Neurology · doi:10.1111/j.1468-1331.2006.01139.x · Cited by 43
“The CNS is particularly vulnerable to oxidative stress because of its high oxygen consumption, abundant lipid content and low antioxidant enzyme levels.”
BackgroundInfluentialPerron, N. R., Beeson, C. C., & Rohrer, B. (2012) · Journal of Bioenergetics and Biomembranes · doi:10.1007/s10863-012-9477-5 · Cited by 42
“Deletions in mitochondrial DNA resulting from ROS oxidation have been shown to increase with age (Mecocci et al. 1993; Richter 1988; Shigenaga et al. 1994), and an agecorrelated decrease in mitochondrial membrane potential has also been observed (Hagen et al. 1997), suggestive of ROS alteration of…”
BackgroundEffects of Dietary Food Components on Cognitive Functions in Older Adults
Ozawa, H., Miyazawa, T., & Miyazawa, T. (2021) · Nutrients · doi:10.3390/nu13082804 · Cited by 44
Dorszewska, J., Florczak, J., Różycka, A., Jaroszewska-Kolecka, J., Trzeciak, W. H., & Kozubski, W. P. (2005) · DNA and Cell Biology · doi:10.1089/dna.2005.24.786 · Cited by 43
Mitochondrial DNA Mutations and Age
Ozawa, T. (1998) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1998.tb09898.x · Cited by 42
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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