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发育期暴露于低浓度汞蒸气后金属硫蛋白-I/II 基因缺失小鼠脑内神经行为改变及基因表达改变。

Neurobehavioral changes and alteration of gene expression in the brains of metallothionein-I/II null mice exposed to low levels of mercury vapor during postnatal development.

机构信息

Faculty of Human Health Science, Hachinohe University, Hachinohe, Japan.

出版信息

J Toxicol Sci. 2011 Oct;36(5):539-47. doi: 10.2131/jts.36.539.

DOI:10.2131/jts.36.539
PMID:22008530
Abstract

This study examined the neurobehavioral changes and alteration in gene expression in the brains of metallothionein (MT)-I/II null mice exposed to low-levels of mercury vapor (Hg(0)) during postnatal development. MT-I/II null and wild-type mice were repeatedly exposed to Hg(0) at 0.030 mg/m(3) (range: 0.023-0.043 mg/m(3)), which was similar to the current threshold value (TLV), for 6 hr per day until the 20th day postpartum. The behavioral effects were evaluated with locomotor activity in the open field (OPF), learning ability in the passive avoidance response (PA) and spatial learning ability in the Morris water maze (MM) at 12 weeks of age. Hg(0)-exposed MT-I/II null mice showed a significant decrease in total locomotor activity in females, though learning ability and spatial learning ability were not affected. Immediately after Hg(0) exposure, mercury concentrations in the brain did not exceed 0.5 µg/g in any animals. Hg(0) exposure resulted in significant alterations in gene expression in the brains of both strains using DNA microarray analysis. The number of altered genes in MT-I/II null mice was higher than that in wild-type mice and calcium-calmodulin kinase II (Camk2a) involved in learning and memory in down-regulated genes was detected. These results provide useful information to elucidate the development of behavioral toxicity following low-level exposure to Hg(0).

摘要

本研究探讨了在发育期低水平汞蒸气(Hg(0))暴露下,金属硫蛋白(MT)-I/II 缺失小鼠的神经行为变化和基因表达改变。MT-I/II 缺失和野生型小鼠反复暴露于 0.030 mg/m³(范围:0.023-0.043 mg/m³)的 Hg(0)中,每天 6 小时,持续到产后第 20 天。12 周龄时,通过旷场(OPF)中的运动活性、被动回避反应(PA)中的学习能力和 Morris 水迷宫(MM)中的空间学习能力评估行为效应。Hg(0)暴露的 MT-I/II 缺失小鼠的雌性总运动活性明显降低,尽管学习能力和空间学习能力不受影响。Hg(0)暴露后,任何动物的大脑中汞浓度均未超过 0.5 µg/g。DNA 微阵列分析显示,Hg(0)暴露导致两种品系的大脑基因表达发生显著改变。MT-I/II 缺失小鼠中改变的基因数量高于野生型小鼠,下调基因中检测到参与学习和记忆的钙调蛋白激酶 II(Camk2a)。这些结果为阐明低水平 Hg(0)暴露后行为毒性的发展提供了有用的信息。

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