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F-344大鼠亚慢性经口暴露于苯并(a)芘[B(a)P]后,剂量依赖性的B(a)P-DNA加合物水平及其持久性。

Dose-dependent benzo(a)pyrene [B(a)P]-DNA adduct levels and persistence in F-344 rats following subchronic dietary exposure to B(a)P.

作者信息

Ramesh Aramandla, Knuckles Maurice E

机构信息

Division of Cancer Biology, Department of Biomedical Sciences, Meharry Medical College, 1005 D.B. Todd Blvd, Nashville, TN 37208, USA.

出版信息

Cancer Lett. 2006 Aug 28;240(2):268-78. doi: 10.1016/j.canlet.2005.09.016. Epub 2005 Nov 8.

Abstract

In order to investigate the relationship between BaP-DNA adduct formation and long-term exposure to benzo(a)pyrene (BaP), DNA adduct levels in liver and lung tissues of male and female F-344 rats subchronically exposed to BaP were determined. Doses of 0, 5, 50, and 100mg/kg BaP, representing control, low, intermediate, and high doses, respectively, were administered in the animal diet over a 90-day period. After dosing, animals were sacrificed, liver and lung tissues were removed, DNA was isolated and analyzed for BaP-induced DNA adducts by the (32)P-postlabeling method using a four-directional thin-layer chromatography system. At low and intermediate BaP doses, DNA adduct levels in the tissues were significantly correlated with exposure. However, at high BaP doses, the dose-DNA adduct relationship became non-linear. Similarly, the relative DNA adducts persistence at intermediate and high doses were significantly higher than that measured at low dose. The low and intermediate dose linearity and high dose non-linearity may be due to saturation of metabolic activation and detoxification enzymes, and DNA repair processes.

摘要

为了研究苯并[a]芘(BaP)-DNA加合物形成与长期接触苯并[a]芘(BaP)之间的关系,测定了亚慢性接触BaP的雄性和雌性F-344大鼠肝脏和肺组织中的DNA加合物水平。分别代表对照、低、中、高剂量的0、5、50和100mg/kg BaP剂量在90天的时间内通过动物饮食给予。给药后,处死动物,取出肝脏和肺组织,分离DNA,并使用四向薄层色谱系统通过(32)P后标记法分析BaP诱导的DNA加合物。在低剂量和中剂量BaP时,组织中的DNA加合物水平与暴露显著相关。然而,在高剂量BaP时,剂量-DNA加合物关系变得非线性。同样,中高剂量下DNA加合物的相对持久性显著高于低剂量下测得的水平。低剂量和中剂量的线性以及高剂量的非线性可能是由于代谢活化和解毒酶以及DNA修复过程的饱和所致。

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