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大鼠气管内滴注环境污染物3-硝基苯并蒽酮后DNA加合物的形成

DNA adduct formation by the environmental contaminant 3-nitrobenzanthrone after intratracheal instillation in rats.

作者信息

Bieler Christian A, Cornelius Michael G, Klein Reinhold, Arlt Volker M, Wiessler Manfred, Phillips David H, Schmeiser Heinz H

机构信息

German Cancer Research Center, Division of Molecular Toxicology, Heidelberg, Germany.

出版信息

Int J Cancer. 2005 Oct 10;116(6):833-8. doi: 10.1002/ijc.21095.

Abstract

3-Nitrobenzanthrone (3-NBA) is an environmental pollutant and suspected human carcinogen found in emissions from diesel and gasoline engines and on the surface of ambient air particulate matter; human exposure to 3-NBA is likely to occur primarily via the respiratory tract. In our study female Sprague Dawley rats were treated by intratracheal instillation with a single dose of 0.2 or 2 mg/kg body weight of 3-NBA. Using the butanol enrichment version of the (32)P-postlabeling method, DNA adduct formation by 3-NBA 48 hr after intratracheal administration in different organs (lung, pancreas, kidney, urinary bladder, heart, small intestine and liver) and in blood was investigated. The same adduct pattern consisting of up to 5 DNA adduct spots was detected by thin layer chromatography in all tissues and blood and at both doses. Highest total adduct levels were found in lung and pancreas (350 +/- 139 and 620 +/- 370 adducts per 10(8) nucleotides for the high dose and 39 +/- 18 and 55 +/- 34 adducts per 10(8) nucleotides for the low dose, respectively) followed by kidney, urinary bladder, heart, small intestine and liver. Adduct levels were dose-dependent in all organs (approximately 10-fold difference between doses). It was demonstrated by high performance liquid chromatography (HPLC) that all 5 3-NBA-derived DNA adducts formed in rats after intratracheal instillation are identical to those formed by other routes of application and are, as previously shown, formed from reductive metabolites bound to purine bases. Although total adduct levels in the blood were much lower (41 +/- 27 and 9.5 +/- 1.9 adducts per 10(8) nucleotides for the high and low dose, respectively) than those found in the lung, they were related to dose and to the levels found in lung. These results show that uptake of 3-NBA by the lung induces high levels of specific DNA adducts in several organs of the rat and an identical adduct pattern in DNA from blood. Therefore, 3-NBA-DNA adducts present in the blood are useful biomarkers for exposure to 3-NBA and may help to assess the effective biological dose in humans exposed to it.

摘要

3-硝基苯并蒽酮(3-NBA)是一种环境污染物,也是一种疑似人类致癌物,存在于柴油和汽油发动机排放物以及环境空气颗粒物表面;人类接触3-NBA可能主要通过呼吸道。在我们的研究中,对雌性斯普拉格-道利大鼠进行气管内滴注,给予单剂量0.2或2mg/kg体重的3-NBA。采用(32)P后标记法的丁醇富集版本,研究了气管内给药48小时后3-NBA在不同器官(肺、胰腺、肾脏、膀胱、心脏、小肠和肝脏)及血液中形成的DNA加合物。通过薄层色谱法在所有组织和血液中以及两个剂量组均检测到由多达5个DNA加合物斑点组成的相同加合物模式。肺和胰腺中的总加合物水平最高(高剂量组每10^8个核苷酸分别为350±139和620±370个加合物,低剂量组每10^8个核苷酸分别为39±18和55±34个加合物),其次是肾脏、膀胱、心脏、小肠和肝脏。所有器官中的加合物水平均呈剂量依赖性(剂量之间约有10倍差异)。高效液相色谱(HPLC)表明,大鼠气管内滴注后形成的所有5种3-NBA衍生的DNA加合物与通过其他给药途径形成的加合物相同,并且如先前所示,是由与嘌呤碱基结合的还原代谢物形成的。尽管血液中的总加合物水平(高剂量组和低剂量组每10^8个核苷酸分别为41±27和9.5±1.9个加合物)远低于肺中的水平,但它们与剂量以及肺中的水平相关。这些结果表明,肺对3-NBA的摄取会在大鼠的多个器官中诱导高水平的特定DNA加合物,并在血液DNA中形成相同的加合物模式。因此,血液中存在的3-NBA-DNA加合物是接触3-NBA的有用生物标志物,并可能有助于评估接触该物质的人类的有效生物剂量。

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