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Mutagenicity of bisphenol A (4,4'-isopropylidenediphenol) in vitro: effects of nitrosylation.

机译:双酚A(4,4'-异丙基二烯二酚)的体外致突变性:亚硝化作用。

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Bisphenol A (4,4'-isopropylidenediphenol) is a common component of polycarbonate plastics and epoxy resins. Since bisphenol A-containing plastics and resins have found uses in food-contact items, its potential migration into foodstuffs and possible health consequences have been the focus of many recent studies. However, the potential mutagenic activation of bisphenol A by nitrosylation has received little attention. Incubation of bisphenol A with sodium nitrite under acidic conditions produced a yellow-brown product. When nitrosylated bisphenol A was tested in the Ames Salmonella/microsome assay at 100 ng to 1 mg/plate, dose-dependent increases in mutagenicity were found in both TA98 and TA100 Salmonella strains. These results indicated the presence of a direct-acting mutagenic activity causing both frameshift and base pair mutations, respectively. When compared to colony formation in untreated controls, the addition of rat liver S9 for metabolic activation had little influence on revertant colony formation. Unreacted bisphenol A dissolved in DMSO, acidic buffer, or inactivated nitrosylation solution showed negligible mutagenicity. When the nature of the mutagenic changes was examined using the Ames II trade mark Assay, a variety of base pair changes was found including T:A to A:T - S9, G:C to A:T +/- S9,C:G to A:T +/- S9 and C:G to G:C +/- S9. Bisphenol A also induced frameshift mutations at G:C sites. In addition, the presence of electrophiles was shown by the production of an intensely coloured orange-red product upon incubation of nitrosylated bisphenol A with the nucleophile 4-(4'-nitrobenzyl)pyridine. These findings suggest that migration of bisphenol A into nitrite containing foodstuffs, or its ingestion in the presence of nitrite, could lead to the formation of mutagenic compounds. Teratogenesis Carcinog. Mutagen. 22: 425-441, 2002. Published 2002 Wiley-Liss, Inc.
机译:双酚A(4,4'-异丙基二烯二酚)是聚碳酸酯塑料和环氧树脂的常见成分。由于含双酚A的塑料和树脂已发现可用于食品接触物品,因此其潜在迁移到食品中以及可能对健康造成的影响已成为许多近期研究的重点。但是,亚硝基化对双酚A的潜在诱变活化作用鲜为人知。在酸性条件下,将双酚A与亚硝酸钠一起孵育,得到黄棕色产物。当在Ames沙门氏菌/微粒体试验中以100 ng至1 mg /板测试亚硝基化双酚A时,在TA98和TA100沙门氏菌菌株中均发现剂量依赖性诱变性增加。这些结果表明存在直接作用的诱变活性,分别引起移码和碱基对突变。与未经处理的对照组的菌落形成相比,添加大鼠肝脏S9进行代谢激活对回复菌落形成几乎没有影响。溶于DMSO,酸性缓冲液或灭活的亚硝基化溶液的未反应双酚A的致突变性可忽略不计。当使用Ames II商标检测法检查诱变变化的性质时,发现了多种碱基对变化,包括T:A到A:T-S9,G:C到A:T +/- S9,C: G到A:T +/- S9和C:G到G:C +/- S9。双酚A还诱导G:C位点的移码突变。另外,在亚硝基化双酚A与亲核试剂4-(4'-硝基苄基)吡啶一起孵育后,生成深红色的橙红色产物表明亲电子试剂的存在。这些发现表明,双酚A迁移到含有亚硝酸盐的食品中,或者在亚硝酸盐存在下摄入,可能导致诱变化合物的形成。致癌作用。诱变剂。 22:425-441,2002。2002年Wiley-Liss,Inc.发布。

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