首页> 外文期刊>Mutation Research: International Journal on Mutagenesis, Chromosome Breakage and Related Subjects >In vivo photochemical skin micronucleus test using a sunlight simulator: Detection of 8-methoxypsoralen and benzo(a)pyrene in hairless mice.
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In vivo photochemical skin micronucleus test using a sunlight simulator: Detection of 8-methoxypsoralen and benzo(a)pyrene in hairless mice.

机译:使用阳光模拟器的体内光化学皮肤微核试验:在无毛小鼠中检测8-甲氧基补骨脂素和苯并(a)re。

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Evaluating in vivo photochemical genotoxicity (photogenotoxicity) or photochemical carcinogenicity (photocarcinogenicity) in the skin that is actually exposed to light is important for estimating the risk of human exposure to chemicals under sunlight. With regard to the skin micronucleus test, Nishikawa et al. developed a reliable technique that is simple and in which the negative control has a stable background. In the present study, we applied 8-methoxypsoralen (8-MOP) and benzo[a]pyrene (B[a]P) to the backs of hairless mice and subjected the mice to irradiation by a sunlight simulator in order to investigate whether this test can detect photogenotoxicity of these chemicals. In the treatment with 8-MOP [0.00075% and 0.0015% (w/v)], a significant increase was observed in the frequency of micronucleated cells only under light irradiation using the sunlight simulator. At a high chemical dose, the frequency of micronucleated cells increased from 48h after the treatment, peaked at 96h, and then decreased at 168h. Furthermore, at 96h with the high dose under light irradiation, we frequently observed cells with nuclear buds. In the treatment with B[a]P [first experiment: 0.025% and 0.05% (w/v); second experiment: 0.005%, 0.01%, and 0.02% (w/v)], a significant increase was observed in the frequency of micronucleated cells at skin-irritating doses [0.01%, 0.02%, 0.025%, and 0.05% (w/v)] at 72 or 96h after the treatment only under light irradiation using the sunlight simulator. In conclusion, photogenotoxicity of 8-MOP and B[a]P was detected in the in vivo photochemical skin micronucleus study.
机译:评估实际暴露在皮肤中的体内光化学遗传毒性(光遗传毒性)或光化学致癌性(光致癌致癌性)对于评估人类在阳光下暴露于化学物质的风险非常重要。关于皮肤微核试验,Nishikawa等。开发了一种简单且可靠的技术,其中阴性对照具有稳定的背景。在本研究中,我们将8-甲氧基补骨脂素(8-MOP)和苯并[a] py(B [a] P)应用于无毛小鼠的背部,并通过阳光模拟器对小鼠进行辐照,以调查是否测试可以检测这些化学物质的光遗传毒性。在使用8-MOP [0.00075%和0.0015%(w / v)]的处理中,仅在使用阳光模拟器的光照射下,观察到微核细胞的频率显着增加。在高化学剂量下,微核细胞的频率从处理后的48h开始增加,在96h达到峰值,然后在168h降低。此外,在高剂量的光照射下96小时,我们经常观察到具有核芽的细胞。在B [a] P治疗中[第一个实验:0.025%和0.05%(w / v);第二个实验:0.005%,0.01%和0.02%(w / v)],在刺激皮肤的剂量[0.01%,0.02%,0.025%和0.05%(w / v)]处理后的72或96小时,仅在使用阳光模拟器进行光照射下。总之,在体内光化学皮肤微核研究中检测到8-MOP和B [a] P的光遗传毒性。

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