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Oxidative damage to DNA during aging: 8-hydroxy-2'-deoxyguanosine in rat organ DNA and urine.

机译:衰老过程中对DNA的氧化损伤:大鼠器官DNA和尿液中的8-hydroxy-2'-deoxyguanosine。

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摘要

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.
机译:DNA的氧化损伤被证明是广泛的,并且可能是与衰老以及与衰老相关的退化性疾病(例如癌症)相关的生理变化的主要原因。已从分离自不同年龄的Fischer 344大鼠的各个器官的DNA中测量了氧化的核苷8-羟基-2'-脱氧鸟苷(oh8dG),这是大约20种已知的氧化DNA损伤产物之一。 oh8dG存在于从所有研究的器官(肝,脑,肾,肠和睾丸)分离的DNA中。 oh8dG的稳态水平范围为每细胞10(6)个脱氧鸟苷残基8到73个残基或每个细胞0.2-2.0 x 10(5)残基。 DNA的oh8dG水平随着年龄的增长在肝脏,肾脏和肠道中增加,但在大脑和睾丸中保持不变。从2个月大和25个月大的大便中获取的尿液中oh8dG的尿排泄量可能从核酸酶活性从DNA修复反映出来,随年龄的增长从分别从481 pmol / kg体重降低到165 pmol / kg体重/日。尿液中还测定了8-羟基鸟嘌呤,它是糖基化酶活性的拟议修复产物。我们估计大鼠中每个细胞每天对DNA的氧化命中率约为9 x 10(4)。结果表明,在肝脏,肾脏和肠的DNA中观察到的oh8dG残基的年龄依赖性积累主要是由于DNA核酸酶活性的缓慢丧失。但是,不能排除氧化性DNA损伤率增加的可能性。

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