Effects of aging and caloric restriction on the genotoxicity of four carcinogens in the in vitro rat hepatocyte/DNA repair assay

J.G. Shaddock , R.J. Feuers , M.W. Chou , R.A. Pegram , D.A. Casciano
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引用次数: 20

Abstract

The effects of aging and chronic caloric restriction (CR) on the genotoxicity of four carcinogens, representing four different classes of chemicals, in the in vitro rat hepatocyte/DNA repair assay were investigated. Hepatocyte cultures were isolated from young, middel-aged, and old male Fischer (F344) rats which were maintained on either an ad libitum (AL) or a CR diet (60% of AL). Hepatocyte cultures from old AL rats, treated with 2-acetylaminofluorene (2-AAF), aflatoxin B1 (AFB1), 7,12-dimethylbenz[a]anthracene (DMBA) and dimethylnitrosamine (DMN), exhibited age-related decreases in DNA repair as compared to young AL rats. By contrast, cultures from young CR rats exhibited significant diet-related decreases in DNA repair with 2-AAF, AFB1, DMBA and DMN, when compared to results from young AL diet-fed rats. Old CR F344 rat derived cultures exhibited no significant age-related dose-dependent decrease in the DNA repair response with any of the chemicals tested. However, in cultures from old CR rats 10.0 μM AFB1 produced an age-related decrease in DNA repair from the response observed in young CR rats. When hepatocytes were isolated from Aroclor 1254-induced rats, increases in DNA repair were observed. These data indicate an age- and diet-related decrease in DNA repair and/or DNA damage and suggest that this decrease is due to a decrease in metabolic activation of these carcinogens to genotoxic species.

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衰老和热量限制对体外大鼠肝细胞/DNA修复实验中四种致癌物遗传毒性的影响
在体外大鼠肝细胞/DNA修复实验中,研究了衰老和慢性热量限制(CR)对四种致癌物质(代表四种不同类型的化学物质)遗传毒性的影响。从年轻、中年和老年雄性Fischer (F344)大鼠中分离肝细胞培养物,这些大鼠分别饲喂自由饮食(AL)或CR饮食(AL的60%)。与年轻AL大鼠相比,用2-乙酰氨基荧光素(2-AAF)、黄曲霉毒素B1 (AFB1)、7,12-二甲基苯[a]蒽(DMBA)和二甲基亚硝胺(DMN)处理老年AL大鼠的肝细胞培养物显示出与年龄相关的DNA修复下降。相比之下,与年轻的AL喂养大鼠相比,来自年轻CR大鼠的培养物显示出与饮食相关的2-AAF、AFB1、DMBA和DMN的DNA修复明显减少。老年CR F344大鼠衍生的培养物在任何化学物质的DNA修复反应中都没有表现出明显的与年龄相关的剂量依赖性下降。然而,在老龄CR大鼠的培养中,10.0 μM AFB1产生了与年轻CR大鼠的反应相关的DNA修复下降。当从Aroclor 1254诱导的大鼠中分离肝细胞时,观察到DNA修复的增加。这些数据表明,DNA修复和/或DNA损伤的减少与年龄和饮食有关,并表明这种减少是由于这些致癌物对遗传毒性物种的代谢激活减少。
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