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In vivo genotoxicity of 1-methylnaphthalene from comprehensive toxicity studies with B6C3F1 gpt delta mice

机译:B6C3F1 gpt delta小鼠的全面毒性研究对1-甲基萘的体内遗传毒性

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1-Methylnaphthalene (1-MN), a constituent of the polycyclic aromatic hydrocarbons (PAHs), is a lung carcinogen in mice. However, conventional genotoxicity tests such as the Ames test and sister chromatid exchange (SCE) test have yielded equivocal results. In the present study, the in vivo genotoxicity of 1-methylnaphthalene (1-MN) together with its toxicological profile was investigated in a 13-week repeated dose toxicity study of 1-MN using B6C3F1 gpt delta mice. In the serum biochemistry, significant increases in AST and ALP were observed in males of the 0.15% 1-MN group. From histopathological examination, the incidence of single cell necrosis in the liver was significantly increased in males of the 0.15% 1-MN group; however, no changes were observed in the lungs, the target organ of 1-MN. In an in vivo mutation assay, no changes in mutant frequencies of gpt and red/gam (Spi-) in lung DNA of 1-MN treated mice were observed at 13 weeks. In addition, there were no significant differences in the proliferating cell nuclear antigen (PCNA)-positive ratios in bronchiolar epithelial cells among the groups for either sex. These results suggest that 1-MN at a carcinogenic dose not induce overt toxicity for any organs and has no in vivo genotoxicity in the lungs.
机译:1-甲基萘(1-MN)是多环芳烃(PAHs)的一种成分,是小鼠的肺致癌物。但是,常规的遗传毒性试验,例如Ames试验和姐妹染色单体交换(SCE)试验,产生了模棱两可的结果。在本研究中,使用B6C3F1 gpt delta小鼠进行了为期13周的1-MN重复剂量毒性研究,研究了1-甲基萘(1-MN)的体内遗传毒性及其毒理学特征。在血清生物化学中,在0.15%1-MN组的男性中观察到AST和ALP显着增加。从组织病理学检查来看,在0.15%1-MN组的男性中,肝脏中单细胞坏死的发生率显着增加。然而,在1-MN的靶器官肺中未观察到变化。在体内突变试验中,在13周时未观察到1-MN处理的小鼠的肺DNA中gpt和red / gam(Spi-)突变频率的变化。此外,男女之间在细支气管上皮细胞中增殖细胞核抗原(PCNA)阳性比率没有显着差异。这些结果表明,致癌剂量的1-MN不会对任何器官产生明显的毒性,并且在肺中没有体内遗传毒性。

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