双酚A(4,4′-异丙基二酚)的体外致突变性:亚硝基化的影响。

Timothy J Schrader, I Langlois, K Soper, W Cherry
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引用次数: 22

摘要

双酚A(4,4′-异丙基二酚)是聚碳酸酯塑料和环氧树脂的常见成分。由于含有双酚a的塑料和树脂已被用于与食品接触的物品,其可能迁移到食品和可能的健康后果已成为许多最近研究的焦点。然而,亚硝基化对双酚A的潜在诱变激活作用却很少受到关注。双酚A与亚硝酸钠在酸性条件下孵育,产物为黄褐色。当亚硝基化双酚A在100 ng至1 mg/板的艾姆斯沙门氏菌/微粒体试验中检测时,发现TA98和TA100沙门氏菌的致突变性均呈剂量依赖性增加。这些结果表明存在直接作用的诱变活性,分别引起移码和碱基对突变。与未处理的对照组相比,添加大鼠肝脏S9进行代谢激活对逆转集落形成的影响很小。未反应的双酚A溶解在DMSO、酸性缓冲液或灭活的亚硝基化溶液中,其致突变性可以忽略不计。当使用Ames II商标试验检查诱变变化的性质时,发现了各种碱基对变化,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还能诱导G:C位点的移码突变。此外,在亚硝基化双酚A与亲核试剂4-(4′-硝基苄基)吡啶孵育后,产生强烈的橙红色产物,表明亲电试剂的存在。这些发现表明,双酚A迁移到含有亚硝酸盐的食物中,或在亚硝酸盐存在的情况下摄入,可能导致致突变化合物的形成。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Mutagenicity of bisphenol A (4,4'-isopropylidenediphenol) in vitro: effects of nitrosylation.

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.

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