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8-羟基鸟嘌呤的形成在低剂量N-亚硝基二乙胺引发大鼠肝癌过程中的作用。

Involvement of 8-hydroxyguanine formation in the initiation of rat liver carcinogenesis by low dose levels of N-nitrosodiethylamine.

作者信息

Nakae D, Kobayashi Y, Akai H, Andoh N, Satoh H, Ohashi K, Tsutsumi M, Konishi Y

机构信息

Department of Oncological Pathology, Cancer Center, Nara Medical University, Kashihara, Japan.

出版信息

Cancer Res. 1997 Apr 1;57(7):1281-7.

PMID:9102214
Abstract

The question of whether 8-hydroxyguanine (8-OHG) formation is involved in initiation by low dose levels of N-nitrosodiethylamine (DEN) was addressed using a rat liver model. Male Fischer 344 rats, 6 weeks of age, were administered single i.p. doses of DEN between 0.001 and 100 mg/kg body weight. The 8-OHG levels in liver DNA were measured within 72 h thereafter in randomly selected rats. The remaining rats were given either no further treatment, partial hepatectomy (PH) at hour 4, or PH with i.p. administration of 500 mg/kg body weight of colchicine on days 1 and 3. A selection procedure was performed between weeks 2 and 4, and the initiating activity of DEN was assessed in terms of development of gamma-glutamyltransferase-positive foci at week 5. The 8-OHG levels in the liver DNA were significantly elevated between hours 6 and 72 in a manner dependent on the DEN dose. Dose-dependent induction of foci was similarly noted with doses of 1-100 and 0.001-100 mg/kg body weight in the non-PH and the PH rats, respectively. The sizes of the foci were also significantly increased in a manner dependent on the DEN doses of 1-100 and 0.001-100 mg/kg body weight in the non-colchicine-treated and the colchicine-treated rats, respectively. Statistically, linear trends of 8-OHG formation due to DEN were different at 0.001-0.1 and 1-100 mg/kg body weight, but the total adducts formed within 72 h of the administration proved to be closely related to the development of foci at the termination. These results indicate that 8-OHG formation in the liver DNA may be involved in DEN initiation of hepatocarcinogenesis even at low dose levels, and that single i.p. doses of 0.001-0.1 and 1-100 mg/kg body weight might exert different effects.

摘要

利用大鼠肝脏模型探讨了低剂量N-亚硝基二乙胺(DEN)引发过程中是否涉及8-羟基鸟嘌呤(8-OHG)的形成。6周龄雄性Fischer 344大鼠经腹腔注射给予0.001至100 mg/kg体重的单次DEN剂量。此后72小时内,随机选取大鼠测量肝脏DNA中的8-OHG水平。其余大鼠要么不再接受进一步处理,要么在第4小时进行部分肝切除术(PH),要么在第1天和第3天进行PH并腹腔注射500 mg/kg体重的秋水仙碱。在第2周和第4周之间进行筛选程序,并在第5周根据γ-谷氨酰转移酶阳性灶的形成评估DEN的引发活性。肝脏DNA中的8-OHG水平在6至72小时之间以依赖于DEN剂量的方式显著升高。在未进行PH和进行PH的大鼠中,分别以1-100和0.001-100 mg/kg体重的剂量观察到了剂量依赖性的灶诱导。在未用秋水仙碱处理和用秋水仙碱处理的大鼠中,灶的大小也分别以依赖于1-100和0.001-100 mg/kg体重的DEN剂量的方式显著增加。统计学上,0.001-0.1和1-100 mg/kg体重时DEN导致的8-OHG形成的线性趋势不同,但给药后72小时内形成的总加合物被证明与终止时灶的形成密切相关。这些结果表明,即使在低剂量水平下,肝脏DNA中8-OHG的形成可能也参与了DEN引发的肝癌发生,并且0.001-0.1和1-100 mg/kg体重的单次腹腔注射剂量可能会产生不同的影响。

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