周苑秀,
李敏杰,
钟伟红,
范瑞芳^,
华南师范大学生命科学学院 广州市亚热带生物多样性与环境生物监测重点实验室, 广州 510631

作者简介: 周苑秀(1992-),女,研究生,研究方向为生态毒理学,E-mail:1097125816@qq.com.

通讯作者: 范瑞芳,20001047@m.scnu.edu.cn

基金项目: 广东省自然科学基金(s2013010013183)
广州市科技计划项目(201510010107)


中图分类号: X171.5

Detection of DNA Damages of Brain Cells in Young Male Mice Induced by Bisphenol A by Comet Assay

Zhou Yuanxiu,
Li Minjie,
Zhong Weihong,
Fan Ruifang^,
Guangzhou Key Laboratory of Subtropical Biodiversity and Biomonitoring, School of Life Science, South China Normal University, Guangzhou 510631, China

Corresponding author: Fan Ruifang,20001047@m.scnu.edu.cn

CLC number: X171.5

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摘要:双酚A是一种日常生活中无处不在的环境雌激素，具有生殖和神经毒性，但低剂量长期暴露对发育期青少年的危害性常常被低估或忽视。本研究以4周龄雄性清洁级小鼠为实验对象，以茶油作为溶媒对照，分别以双酚A浓度为0 μg·mL^-1、0.1 μg·mL^-1、10 μg·mL^-1和1 000 μg·mL^-1的茶油灌胃小鼠8周，然后利用彗星电泳法检测各组小鼠脑细胞的DNA损伤。结果显示，不同浓度双酚A暴露8周后，彗星电泳图像显示小鼠脑细胞DNA出现不同程度的损伤，随着暴露剂量的增加，带有彗尾的脑细胞比率从对照组小鼠的9.5%分别升高到暴露组小鼠的34.5%、36.0%和50.5%，细胞总体的尾部DNA含量、尾长和尾矩也都逐渐增加，而且各双酚A暴露组小鼠与溶媒对照组小鼠脑细胞都具有显著性差异(P<0.01)，这说明中长期双酚A暴露(包括低浓度环境暴露)会导致雄性幼龄小鼠脑细胞的DNA损伤。
关键词: 双酚A/
小鼠/
脑细胞/
DNA损伤/
雄性/
幼龄

Abstract:Bisphenol A (BPA) is an environmental xenoestrogenic endocrine disruptor and has shown detectable toxicity on biological systems, including the reproduction system, immune system, endocrine system and neurological development. However, the neurotoxicity of low dose BPA to children and youth is often underestimated and few studies were conducted on this aspect. We herein examine the effects of low dose BPA exposure on DNA damage of brain cells of male mice. The adolescent male mice at the age of 4 weeks were divided into four groups, including the control group and three exposure groups, and chronically received systematically varying BPA treatments (0 μg·mL^-1, 0.1 μg·mL^-1, 10 μg·mL^-1 and 1 000 μg·mL^-1 in tea oil) for 8 weeks. Comet assay was then employed to detect the DNA damages of the brain cells in these mice. After the treatments with BPA, the comet percentages of brain cells increased significantly from 9.5% in the control group to 34.5%, 36.0% and 50.5% in the three exposure groups respectively, consistent with raised percentages of tail DNA, tail length and tail moment in brain cells. The results show that mid-long term exposure to the low dose BPA lead to DNA damage of brain cells in adolescent male mice and the damage levels increase with the increasing BPA concentrations.
Key words:bisphenol A/
mice/
brain cells/
DNA damage/
male/
young.