Yax Thakkar, Tetyana Kobets, Anne Marie Api, Jian-Dong Duan, Gary M. Williams
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In contrast, p-methoxy cinnamaldehyde, which was also negative in the in vivo genotoxicity assays, produced evidence of DNA damage, including DNA strand breaks and DNA adducts in CEGA. However, no increase in the micronucleus formation in blood was reported in the HET-MN study. Such variation in responses between the CEGA and HET-MN assay can be attributed to differences in the dosing protocols. Pretreatment with a glutathione precursor, N-acetyl cysteine, negated positive outcomes produced by p-methoxy cinnamaldehyde in CEGA, indicating that difference in response observed in the chicken egg and rodent models can be attributed to rapid glutathione depletion. 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引用次数: 0
摘要
采用鸡卵遗传毒性试验(CEGA)和母鸡卵微核试验(HET-MN)分别评估了用作香料的四种α,β-不饱和醛类(2-苯基-2-丁烯醛、壬-2-反式-6-顺式-二烯醛、2-甲基-2-戊烯醛和对甲氧基肉桂醛)的遗传毒性和致染色体分裂/致新生殖细胞分裂潜能。选择材料的依据是其化学结构以及之前在监管机构体外和/或体内遗传毒性测试中的评估结果。三种受测材料(2-苯基-2-丁烯醛、壬-2-反式-6-顺式二烯醛和 2-甲基-2-戊烯醛)在 CEGA 和 HET-MN 试验中均呈阴性。这些发现与体内遗传毒性检测的结果一致。相反,对甲氧基肉桂醛在体内遗传毒性试验中也呈阴性,但在 CEGA 中却产生了 DNA 损伤的证据,包括 DNA 链断裂和 DNA 加合物。然而,在 HET-MN 研究中,血液中的微核形成没有增加。CEGA 和 HET-MN 检测中反应的这种差异可归因于给药方案的不同。用谷胱甘肽前体 N-乙酰半胱氨酸进行预处理可抵消 CEGA 中对甲氧基肉桂醛产生的积极结果,这表明在鸡卵和啮齿动物模型中观察到的反应差异可归因于谷胱甘肽的快速消耗。总之,我们的研究结果支持这样的结论,即 CEGA 和/或 HET-MN 可被视为动物试验的潜在替代方法,作为评估体外有遗传毒性证据的香料的遗传毒性潜力的后续策略。
Assessment of genotoxic potential of fragrance materials in the chicken egg assays
The genotoxic and clastogenic/aneugeneic potentials of four α,β-unsaturated aldehydes, 2-phenyl-2-butenal, nona-2-trans-6-cis-dienal, 2-methyl-2-pentenal, and p-methoxy cinnamaldehyde, which are used as fragrance materials, were assessed using the Chicken Egg Genotoxicity Assay (CEGA) and the Hen's egg micronucleus (HET-MN) assay, respectively. Selection of materials was based on their chemical structures and the results of their previous assessment in the regulatory in vitro and/or in vivo genotoxicity test battery. Three tested materials, 2-phenyl-2-butenal, nona-2-trans-6-cis-dienal, and 2-methyl-2-pentenal, were negative in both, CEGA and HET-MN assays. These findings were congruent with the results of regulatory in vivo genotoxicity assays. In contrast, p-methoxy cinnamaldehyde, which was also negative in the in vivo genotoxicity assays, produced evidence of DNA damage, including DNA strand breaks and DNA adducts in CEGA. However, no increase in the micronucleus formation in blood was reported in the HET-MN study. Such variation in responses between the CEGA and HET-MN assay can be attributed to differences in the dosing protocols. Pretreatment with a glutathione precursor, N-acetyl cysteine, negated positive outcomes produced by p-methoxy cinnamaldehyde in CEGA, indicating that difference in response observed in the chicken egg and rodent models can be attributed to rapid glutathione depletion. Overall, our findings support the conclusion that CEGA and/or HET-MN can be considered as a potential alternative to animal testing as follow-up strategies for assessment of genotoxic potential of fragrance materials with evidence of genotoxicity in vitro.