Proceedings of the National Academy of Sciences · 1990 · 1.1K citations · 31 references
Life SciencesBiochemistryMolecular BiologyAgingCellular MetabolismDna RepairCellular AgingDna DamageGenetics Of AgingGenotoxicity AssessmentOxidative Damage To BiomoleculesOxidative StressAge-related Oxidative StressDna Oxidative AdductsOxidative Dna DamageOxidative Dna LesionsOxidative Dna RepairOxidative Strand BreaksPhysiological Changes In Aging
Oxidative DNA damage is extensive and may drive aging‑related physiological changes and degenerative diseases such as cancer. The study quantified 8‑hydroxy‑2′‑deoxyguanosine in organ DNA and its repair product 8‑hydroxyguanine in urine of Fischer 344 rats across ages. oh8dG was detected in all organs, with age‑related increases in liver, kidney, and intestine but not brain or testes; urinary excretion declined with age, suggesting reduced DNA repair, and the data imply about 9 × 10⁴ oxidative hits per cell per day.
Oxidative damage to DNA is shown to be extensive and could be a major cause of the physiological changes associated with aging and the degenerative diseases related to aging such as cancer. The oxidized nucleoside, 8-hydroxy-2'-deoxyguanosine (oh8dG), one of the approximately 20 known oxidative DNA damage products, has been measured in DNA isolated from various organs of Fischer 344 rats of different ages. oh8dG was present in the DNA isolated from all the organs studied: liver, brain, kidney, intestine, and testes. Steady-state levels of oh8dG ranged from 8 to 73 residues per 10(6) deoxyguanosine residues or 0.2-2.0 x 10(5) residues per cell. Levels of oh8dG in DNA increased with age in liver, kidney, and intestine but remained unchanged in brain and testes. The urinary excretion of oh8dG, which presumably reflects its repair from DNA by nuclease activity, decreased with age from 481 to 165 pmol per kg of body weight per day for urine obtained from 2-month- and 25-month-old rats, respectively. 8-Hydroxyguanine, the proposed repair product of a glycosylase activity, was also assayed in the urine. We estimate approximately 9 x 10(4) oxidative hits to DNA per cell per day in the rat. The results suggest that the age-dependent accumulation of oh8dG residues observed in DNA from liver, kidney, and intestine is principally due to the slow loss of DNA nuclease activity; however, an increase in the rate of oxidative DNA damage cannot be ruled out.
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Free radicals in biology and medicine
General Pharmacology The Vascular System · 1991 · 17.2K citations
Hydroperoxide metabolism in mammalian organs.
B Chance, Helmut Sies, A Boveris · Physiological Reviews · 1979 · 5.8K citations
Denham Harman · Proceedings of the National Academy of Sciences · 1981 · 1.9K citations · Full text
Life Sciences, Immunology, Nutrition +17