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环境致癌物苯并[a]芘与食物源致癌物二元混合物的剂量依赖性协同和拮抗突变反应。

Dose-dependent synergistic and antagonistic mutation responses of binary mixtures of the environmental carcinogen benzo[a]pyrene with food-derived carcinogens.

机构信息

Computational and Systems Medicine, Imperial College London, London, UK.

Genetic Toxicology, MSAS, Drug Safety and Metabolism, IMED Biotech Unit, AstraZeneca, Cambridge, UK.

出版信息

Arch Toxicol. 2018 Dec;92(12):3459-3469. doi: 10.1007/s00204-018-2319-4. Epub 2018 Sep 26.

Abstract

Cooking food at high temperatures produces genotoxic chemicals and there is concern about their impact on human health. DNA damage caused by individual chemicals has been investigated but few studies have examined the consequences of exposure to mixtures as found in food. The current study examined the mutagenic response to binary mixtures of benzo[a]pyrene (BaP) with glycidamide (GA), BaP with acrylamide (AC), or 2-amino-1-methyl-6-phenylimidazo[4,5-b]pyridine (PhIP) with GA at human-relevant concentrations (sub-nM). The metabolically competent human MCL-5 cells were exposed to these chemicals individually or in mixtures and mutagenicity was assessed at the thymidine kinase (TK) locus. Mixture exposures gave dose-responses that differed from those for the individual chemicals; for the BaP-containing mixtures, an increased mutation frequency (MF) at low concentration combinations that were not mutagenic individually, and decreased MF at higher concentration combinations, compared to the calculated predicted additive MF of the individual chemicals. In contrast, the mixture of PhIP with GA did not increase MF above background levels. These data suggest BaP is driving the mutation response and that metabolic activation plays a role; in mixtures with BaP the increased/decreased MF above/below the expected additive MF the order is PhIP > AC > GA. The increase in MF at some low concentration combinations that include BaP is interesting and supports our previous work showing a similar response for BaP with PhIP, confirming this response is not limited to the BaP/PhIP combination. Moreover, the lack of a mutation response for PhIP with GA relative to the response of the individual chemicals at equivalent doses is interesting and may represent a potential avenue for reducing the risk of exposure to environmental carcinogens; specifically, removal of BaP from the mixture may reduce the mutation effect, although in the context of food this would be significantly challenging.

摘要

高温烹饪食物会产生遗传毒性化学物质,人们担心这些化学物质会对人类健康造成影响。虽然已经研究了个别化学物质引起的 DNA 损伤,但很少有研究探讨食物中存在的混合物暴露的后果。本研究在人类相关浓度(亚纳摩尔)下,检查了苯并[a]芘(BaP)与缩水甘油酰胺(GA)、BaP 与丙烯酰胺(AC)或 2-氨基-1-甲基-6-苯基咪唑[4,5-b]吡啶(PhIP)与 GA 的二元混合物对致突变性的反应。代谢能力强的人 MCL-5 细胞单独或混合接触这些化学物质,并在胸苷激酶(TK)基因座评估致突变性。混合物暴露产生的剂量反应与个别化学物质的反应不同;对于含有 BaP 的混合物,在低浓度组合下,突变频率(MF)增加,但单独作用时无致突变性,在高浓度组合下,MF 降低,与个别化学物质的预期加性 MF 相比。相比之下,PhIP 与 GA 的混合物并未使 MF 高于背景水平。这些数据表明 BaP 是导致突变反应的原因,并且代谢激活发挥了作用;在与 BaP 混合的混合物中,MF 高于/低于预期加性 MF 的增加/减少顺序为 PhIP>AC>GA。BaP 存在的某些低浓度组合中 MF 增加的情况很有趣,并且支持我们之前的工作,该工作显示 BaP 与 PhIP 有类似的反应,证实这种反应不仅限于 BaP/PhIP 组合。此外,与等效剂量下个别化学物质的反应相比,PhIP 与 GA 的混合物没有致突变反应是很有趣的,这可能代表了降低接触环境致癌物风险的潜在途径;具体来说,从混合物中去除 BaP 可能会降低突变效应,尽管在食物的背景下,这将是一个重大挑战。

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