Schrader Timothy J, Langlois I, Soper K, Cherry W
Toxicology Research Division, Food Directorate, Health Canada, Banting Research Centre,Tunney's Pasture, Ottawa, Ontario, Canada.
Teratog Carcinog Mutagen. 2002;22(6):425-41. doi: 10.1002/tcm.10039.
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.
双酚A(4,4'-异亚丙基二苯酚)是聚碳酸酯塑料和环氧树脂的常见成分。由于含双酚A的塑料和树脂已用于食品接触物品,其向食品中的潜在迁移以及可能的健康后果一直是近期许多研究的重点。然而,双酚A通过亚硝化作用的潜在诱变活化很少受到关注。在酸性条件下将双酚A与亚硝酸钠一起孵育会产生一种黄棕色产物。当在Ames沙门氏菌/微粒体试验中以100 ng至1 mg/平板的浓度测试亚硝化双酚A时,在TA98和TA100沙门氏菌菌株中均发现致突变性呈剂量依赖性增加。这些结果表明存在直接作用的诱变活性,分别导致移码突变和碱基对突变。与未处理对照中的菌落形成相比,添加大鼠肝脏S9进行代谢活化对回复菌落形成的影响很小。溶解于二甲基亚砜、酸性缓冲液或失活的亚硝化溶液中的未反应双酚A显示出可忽略不计的致突变性。当使用Ames II商标试验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以及C:G到G:C +/- S9。双酚A还在G:C位点诱导移码突变。此外,亚硝化双酚A与亲核试剂4-(4'-硝基苄基)吡啶孵育时产生强烈橙色-红色产物,表明存在亲电试剂。这些发现表明双酚A迁移到含亚硝酸盐的食品中,或在存在亚硝酸盐的情况下摄入双酚A,可能导致诱变化合物的形成。