Lu Chunwei, Zhao Fenghong, Sun Di, Zhong Yuan, Yu Xiaoyun, Li Gexin, Lv Xiuqiang, Sun Guifan, Jin Yaping
Section of Health Testing, School of Public Health, China Medical University, Shenyang, Liaoning, People's Republic of China.
Environ Toxicol. 2014 May;29(7):797-803. doi: 10.1002/tox.21808. Epub 2012 Aug 21.
The aim of this study was to compare the risk from exposure to arsenate (iAs(V) ) or arsenite (iAs(III) ) at the early life. Mother mice were exposed to equimolar dose of iAs(V) and iAs(III) via drinking water during gestation and lactation. Their offspring continually drank the same water after weaning. Levels of speciated arsenic in both liver and brain were analyzed by hydride generation of volatile arsines and atomic absorption spectrophotometry (HG-AAS). In the liver, inorganic arsenic (iAs) levels significantly increased from postnatal day (PND) 15, and those on PND 35 were significantly higher than on PND 15 and 21 in iAs(III) exposed mice, but iAs levels did not significantly differ until PND 35 in iAs(V) exposed mice; Furthermore, all speciated arsenic levels on PND 35 and dimethylarsinic acid (DMA) levels on PND 1 were significantly higher in iAs(III) exposed mice than those in iAs(V) exposed mice. In the brain, iAs levels increased significantly on PND 21, but those declined sharply on PND 35 in either iAs(III) or iAs(V) exposed mice, however the mean difference between the two exposure groups was not significant; whereas DMA levels in iAs(III) exposed mice were significantly higher than those in iAs(V) exposed mice on both PND 1 and 35. In conclusion, findings from this study suggested that iAs(III) was preferentially accumulated into liver, and expected to result in more efficient methylation capacity than iAs(V) ; either iAs(V) or iAs(III) might be accumulated in the brain readily, when immature blood brain barrier can not limit it into brain. Hence, exposure to either iAs(V) or iAs(III) at the early life may increase the risk of iAs exposure in the brain.
本研究的目的是比较生命早期暴露于砷酸盐(iAs(V))或亚砷酸盐(iAs(III))的风险。母鼠在妊娠和哺乳期通过饮用水接触等摩尔剂量的iAs(V)和iAs(III)。它们的后代断奶后继续饮用相同的水。通过挥发性胂的氢化物发生和原子吸收分光光度法(HG-AAS)分析肝脏和大脑中砷的形态水平。在肝脏中,无机砷(iAs)水平从出生后第15天(PND)开始显著增加,在iAs(III)暴露组小鼠中,PND 35时的iAs水平显著高于PND 15和21时,但在iAs(V)暴露组小鼠中,直到PND 35时iAs水平才出现显著差异;此外,iAs(III)暴露组小鼠PND 35时所有砷形态水平以及PND 1时二甲基胂酸(DMA)水平均显著高于iAs(V)暴露组小鼠。在大脑中,iAs(III)或iAs(V)暴露组小鼠的iAs水平在PND 21时显著增加,但在PND 35时急剧下降,然而两个暴露组之间的平均差异不显著;而在PND 1和35时,iAs(III)暴露组小鼠的DMA水平均显著高于iAs(V)暴露组小鼠。总之,本研究结果表明,iAs(III)优先在肝脏中蓄积,且预期其甲基化能力比iAs(V)更强;当未成熟的血脑屏障无法限制其进入大脑时,iAs(V)或iAs(III)都可能容易在大脑中蓄积。因此,生命早期暴露于iAs(V)或iAs(III)可能会增加大脑中iAs暴露的风险。