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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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Duca, G. G. (2012) · Springer series in chemical physics · doi:10.1007/978-3-642-24629-6_4
Mitochondrial Inheritance and Function in the Lifespan Control of Budding Yeast
McFaline-Figueroa, J. R. (2012) · doi:10.7916/d8zw1t00
INCREASED OXIDATIVE DAMAGE TO DNA AND THE EFFECTS ON MITOCHONDRIAL PROTEIN IN ALZHEIMER'S DISEASE
Wang, J. (2006) · UKnowledge (University of Kentucky)
Gururaj Joshi, A. (2006) · UKnowledge (University of Kentucky)
Opii, W. O. (2006) · UKnowledge (University of Kentucky)
Mitochondrial dysfunction in ageing and degenerative disease
Wredenberg, A. (2007) · Figshare
OXIDATIVE STRESS AND MITOCHONDRIAL DYSFUNCTION IN TRAUMATIC BRAIN INJURY IN AGING
Shao, C. (2007) · UKnowledge (University of Kentucky)
Chapter 6 Pathophysiology of Mitochondrial Disease as Illuminated by Animal Models
Wallace, D. (2002) · Blue books of practical neurology · doi:10.1016/s1877-3419(09)70065-0
Pereira, C. P. M. (2014) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/d.46.2014.tde-30092014-084746
Chapter 4 Genetic Abnormalities in Amyotrophic Lateral Sclerosis
Kasarskis, E. J., & Clair, D. K. S. (1999) · Advances in cell aging and gerontology · doi:10.1016/s1566-3124(08)60024-3
The regulation of RNA Polymerase I-mediated transcription in forebrain neurons.
Smith, S. C. (2012) · ThinkIR: The University of Louisville's Institutional Repository (University of Louisville) · doi:10.18297/etd/1350
Richter, C. (1999) · Rejuvenation Research · doi:10.1089/rej.1.1999.2.217
“Similar values were later obtained by others, and it was also reported that the oxidative load of mtDNA increases with increasing age.29 Since 8-OHdG is just one of about 30 different base modifications it appeared that oxidative damage to mtDNA is enormous.”
Mitochontrial DNA copy number in peripheral blood in polycystic ovarian syndrome
Lee, J., Lee, S. H., Chung, D. J., Kim, E. S., Ryu, C. S., & Kang, S. (2010) · Fertility and Sterility · doi:10.1016/j.fertnstert.2010.07.746
“[10] Mecocci P, MacGarvey U, Kaufman AE, et al.”
BackgroundHong, Q., Guo-qin, J., Zhao, W., & Xue-li, Z. (2003) · Chinese Journal of Integrative Medicine · doi:10.1007/bf02836355
Melatonin and mitochondria in aging
Dong, W., Huang, F. P., & He, H. (2010) · Frontiers in Biology · doi:10.1007/s11515-010-0730-1
“Thus, the level of DNA damage in aging humans is 10-fold greater in the mitochondrion than in the nucleus (Mecocci et al., 1993).”
BackgroundAging, Energy and Alzheimer’s Disease
Bowling, A. C., & Beal, M. F. (1981) · Springer eBooks · doi:10.1007/978-3-662-01135-5_21
Yang, W. (2006) · OakTrust (Texas A&M University Libraries)
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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