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Age-associated change in mitochondrial DNA damage
E K Hudson1, B A Hogue, N C Souza-Pinto
1Laboratory of Molecular Genetics, Gerontology Research Center, NIA, NIH, Baltimore, MD 21224-6823, USA.
Abstract:
There is an age-associated decline in the mitochondrial function of the Wistar rat heart. Previous reports from this lab have shown a decrease in mitochondrial cytochrome c oxidase (COX) activity associated with a reduction in COX gene and protein expression and a similar decrease in the rate of mitochondrial protein synthesis. Damage to mitochondrial DNA may contribute to this decline. Using the HPLC-Coularray system (ESA, USA), we measured levels of nuclear and mitochondrial 8-oxo-2'-deoxyguanosine (8-oxodG) from 6-month (young) and 23-month-old (senescent) rat liver DNA. We measured the sensitivity of the technique by damaging calf thymus DNA with photoactivated methylene blue for 30s up to 2h. The levels of damage were linear over the entire time course including the shorter times which showed levels comparable to those expected in liver. For the liver data, 8-oxodG was reported as a fraction of 2-deoxyguanosine (2-dG). There was no change in the levels of 8-oxodG levels in the nuclear DNA from 6 to 23-months of age. However, the levels of 8-oxodG increased 2.5-fold in the mitochondrial DNA with age. At 6 months, the level of 8-oxodG in mtDNA was 5-fold higher than nuclear and increased to approximately 12-fold higher by 23 months of age. These findings agree with other reports showing an age-associated increase in levels of mtDNA damage; however, the degree to which it increases is smaller. Such damage to the mitochondrial DNA may contribute to the age-associated decline in mitochondrial function.
Insights
Aging Wistar rats show increased mitochondrial DNA damage, specifically 8-oxo-2'-deoxyguanosine (8-oxodG), which may explain age-related declines in heart mitochondrial function.
Area of Science:
- Gerontology
- Molecular Biology
- Cardiovascular Research
Background:
- Mitochondrial dysfunction is linked to aging.
- Previous studies show decreased cytochrome c oxidase (COX) activity and protein synthesis in aging rat hearts.
- Mitochondrial DNA (mtDNA) damage is a potential contributor to this decline.
Purpose of the Study:
- To investigate age-associated changes in oxidative damage to nuclear and mitochondrial DNA in Wistar rat liver.
- To quantify levels of 8-oxo-2 -deoxyguanosine (8-oxodG), a marker of oxidative DNA damage, in young and senescent rats.
Main Methods:
- HPLC-Coularray system used to measure 8-oxodG in nuclear and mitochondrial DNA from 6-month (young) and 23-month-old (senescent) Wistar rats.
- Calf thymus DNA was damaged to validate technique sensitivity.
- 8-oxodG levels reported as a fraction of 2-deoxyguanosine (2-dG).
Main Results:
- No significant change in nuclear DNA 8-oxodG levels with age.
- A 2.5-fold increase in mitochondrial DNA 8-oxodG levels in senescent rats compared to young rats.
- Mitochondrial 8-oxodG was significantly higher than nuclear 8-oxodG, increasing from 5-fold to 12-fold with age.
Conclusions:
- Age-associated oxidative damage to mitochondrial DNA increases significantly in Wistar rat liver.
- This elevated mtDNA damage may contribute to the decline in mitochondrial function observed with aging.
- Findings support the role of mtDNA integrity in the aging process and cardiovascular health.