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吸入暴露后,苯乙烯单体不会在小鼠肝脏中诱导非程序性DNA合成。

Styrene monomer does not induce unscheduled DNA synthesis in the mouse liver following inhalation exposure.

作者信息

Clay Philip

机构信息

Syngenta CTL, Alderley Park, Macclesfield, Cheshire SK10 4TJ, UK.

出版信息

Mutagenesis. 2004 Nov;19(6):489-92. doi: 10.1093/mutage/geh062.

Abstract

Styrene monomer is a commercially important chemical used extensively in the production of plastics. It has been shown to induce lung tumours in the mouse via the inhalation route. Styrene monomer has shown a low reactivity with DNA and also a lack of genotoxic response in the mouse lung in vivo. Together with the fact that the mouse lung tumours were late occurring and mostly benign, which suggest a promotional effect rather than initiation, these factors have led to a suggestion that the tumours may not be of genotoxic origin. The studies examining the genotoxicity of styrene monomer in vivo have to date been predominantly cytogenetic assessments, although low levels of DNA adducts have been reported in the mouse liver and lung. In order to extend this evaluation, a mouse liver unscheduled DNA synthesis study has been performed to assess the ability of styrene monomer to induce DNA damage/repair. The negative response observed in this assay is consistent with the theory that tumours observed in mouse oncogenicity studies are non-genotoxic in origin.

摘要

苯乙烯单体是一种在商业上很重要的化学品,广泛用于塑料生产。已表明它通过吸入途径可在小鼠体内诱发肺肿瘤。苯乙烯单体与DNA的反应性较低,并且在小鼠肺内体内也缺乏遗传毒性反应。再加上小鼠肺肿瘤发生较晚且大多为良性,这表明是促进作用而非引发作用,这些因素导致有人提出肿瘤可能并非源于遗传毒性。迄今为止,研究苯乙烯单体体内遗传毒性的研究主要是细胞遗传学评估,尽管在小鼠肝脏和肺中已报告有低水平的DNA加合物。为了扩展这一评估,已进行了一项小鼠肝脏非程序性DNA合成研究,以评估苯乙烯单体诱导DNA损伤/修复的能力。该试验中观察到的阴性反应与小鼠致癌性研究中观察到的肿瘤源于非遗传毒性的理论一致。

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