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以小鼠微核试验作为评估砷在人体参考剂量下遗传毒性潜能的替代方法。

Mouse micronucleus assay as a surrogate to assess genotoxic potential of arsenic at its human reference dose.

机构信息

Toxicogenetics Laboratory, Department of Zoology, Patna University, Patna 800 005, India.

出版信息

Chemosphere. 2013 Jan;90(3):993-7. doi: 10.1016/j.chemosphere.2012.07.021. Epub 2012 Aug 18.

Abstract

Exposure to high contents of arsenic (a genotoxic carcinogen) in humans through drinking water is one of the most serious concerns in many parts of the world including India. The United States Environmental Protection Agency (USEPA) has recommended a permissible limit of daily exposure in humans to arsenic as its reference dose (0.3 μg kg(-1) d(-1)) with almost no likelihood of any adverse effect. The present work was a quantitative assessment of the genotoxic potential of arsenic at the exposure level of its human reference dose through micronucleus (MN) assay in mice. The animals were exposed to various doses of arsenic through oral gavaging for 15 consecutive days. Significant increases in the frequency of micronucleated erythrocytes were observed in mice upon exposure to arsenic which occurred even at its human reference dose and in a dose-dependent manner. The study of the genotoxic potential of arsenic in humans at lower exposure levels (including its human reference dose) is, therefore, highly desirable for risk assessment and hazard identification.

摘要

人类通过饮用水暴露于高浓度的砷(一种遗传毒性致癌物)是世界上许多地区(包括印度)最严重的问题之一。美国环境保护署(USEPA)已建议将人类每日砷暴露的允许限量设定为其参考剂量(0.3μg/kg/d),几乎没有任何不良影响的可能性。本研究通过小鼠微核(MN)试验对砷在其人类参考剂量暴露水平下的遗传毒性潜力进行了定量评估。动物通过口服灌胃连续 15 天接触不同剂量的砷。结果发现,即使在人类参考剂量下,砷暴露也会导致小鼠红细胞微核频率显著增加,且呈剂量依赖性。因此,在较低暴露水平(包括其人类参考剂量)下研究砷对人类的遗传毒性潜力对于风险评估和危害识别是非常必要的。

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