衰老过程中8-羟基-2 ' -脱氧鸟苷的非线性积累,这是氧化DNA损伤的标志

Takao Kaneo, Shoichi Tahara, Mitsuyoshi Matsuo
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引用次数: 189

摘要

DNA损伤似乎与衰老和与年龄相关的退行性疾病的病因学有关。这项研究的目的是研究衰老过程中DNA损伤的变化。氧化核苷8-羟基-2 ' -脱氧鸟苷(8-OHdG)是氧化应激损伤DNA的生物标志物。测定了不同年龄雄性Fischer 344大鼠脑、心、肝、肾核DNA中8-OHdG的含量。采用高效液相色谱-电化学检测方法,在+350 mV的应用电位下,8-OHdG在fmol水平上具有选择性和灵敏度。心脏、肝脏和肾脏中8-OHdG的含量(以核DNA中脱氧鸟苷的比例表示)在2 - 24个月期间保持稳定,然后逐渐增加。2 ~ 27月龄大鼠脑DNA中8-OHdG含量无变化,30月龄大鼠脑DNA中8-OHdG含量明显升高。与2-24月龄大鼠相比,30月龄大鼠所有器官核DNA中8-OHdG的含量显著增加了2倍。这些结果表明,大鼠器官DNA中8-OHdG的积累始于24个月以上。
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Non-linear accumulation of 8-hydroxy-2′-deoxyguanosine, a marker of oxidized DNA damage, during aging

Damage to DNA seems to be involved in aging and the etiology of age-associated degenerative disease. The purpose of this study is to examine changes in DNA damage during aging. Am oxidized nucleoside, 8-hydroxy-2′-deoxyguanosine (8-OHdG), is a proposed biomarker for DNA damaged by oxidative stress. The content of 8-OHdG in nuclear DNA isolated from brain, heart, liver, and kidneys of male Fischer 344 rats of different ages was measured. 8-OHdG can be detected selectivity and sensitivity at the fmol level by high performance liquid chromatography-electrochemical detection at an applied ptential of +350 mV. The amount of 8-OHdG, expressed as the ratio oto deoxyguanosine in nuclear DNA, in heart, liver, and kidney remained steady from 2 to 24 months and then increased progressively. The content of 8-OHdG in teh DNA in brain showed no changes from 2 to 27 months, but was significantly higher in 30 month-old rats. There was a significant 2-fold increase in the amount of 8-OHdG in the nuclear DNA of all organs tested in 30 month-old rats as compared to 2–24 month-old rats. These results indicate that the accumulation of 8-OHdG in the DNA of rat organs begins at ages above 24 months.

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Publisher's note Editorial An accessory protein enhances both DNA binding and activity of DNA polymerase α isolated from normal, but not transformed, human fibroblasts Differences in the spectrum of spontaneous mutations in the hprt gene between tumor cells of the microsatellite mutator phenotype Spermatid micronucleus analysis of aging effects in hamsters
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