Environmental Chemistry Division, National Institute for Environmental Studies, Onogawa 16-2, Tsukuba, Ibaraki 305-8506, Japan.
Neurotoxicol Teratol. 2012 Jan-Feb;34(1):143-51. doi: 10.1016/j.ntt.2011.08.007. Epub 2011 Aug 22.
Citizens in an area of Kamisu City, Ibaraki, Japan had exhibited unusual health problems, and pollution of well water by diphenylarsinic acid (DPAA) was found in the area. We examined the effects of DPAA on various behaviors in mice. DPAA was administered to mice through free intake of drinking water for 27 weeks (subchronic exposure) or 57 weeks (chronic exposure), and behavior was examined during exposure. DPAA at 30-100 ppm increased ambulatory activity and the response rate of the shuttle type discrete conditioned avoidance response of mice. DPAA reduced coordination ability on the fixed rod at 100 ppm. DPAA at 7.5-15 ppm also reduced coordination on the rotating rod, although these doses of DPAA did not affect coordination on the fixed rod. Chronic exposure to 7.5-15 ppm of DPAA produced anti-anxiety-like effects in the elevated plus maze test, whereas subchronic exposure to 100 ppm of DPAA produced anxiogenic-like effects. Neither subchronic nor chronic exposure to 7.5-100 ppm of DPAA affected learning ability and/or memory, as evaluated using the passive avoidance response. Exposure to 15-30 ppm of DPAA for 52 weeks did not alter weights of the cerebrum and cerebellum or amounts of neuron marker protein TUJ-1 or astrocyte marker protein glial fibrillary acidic protein in the cerebellum of mice. Behavioral effects observed in mice seem relevant to symptoms observed in patients from Kamisu City.
日本茨城县磐城市的一个地区的市民出现了异常健康问题,发现该地区的井水受到二苯胂酸(DPAA)的污染。我们研究了 DPAA 对小鼠各种行为的影响。DPAA 通过自由摄入饮用水,在 27 周(亚慢性暴露)或 57 周(慢性暴露)期间给予小鼠,并在暴露期间检查行为。30-100ppm 的 DPAA 增加了小鼠的活动量和穿梭型离散条件回避反应的反应率。100ppm 的 DPAA 降低了小鼠在固定棒上的协调能力。7.5-15ppm 的 DPAA 也降低了在旋转棒上的协调能力,尽管这些剂量的 DPAA 对固定棒上的协调能力没有影响。慢性暴露于 7.5-15ppm 的 DPAA 在高架十字迷宫测试中产生抗焦虑样效应,而亚慢性暴露于 100ppm 的 DPAA 产生焦虑样效应。亚慢性和慢性暴露于 7.5-100ppm 的 DPAA 均未影响被动回避反应评估的学习能力和/或记忆。52 周暴露于 15-30ppm 的 DPAA 不会改变小鼠大脑和小脑的重量,或小脑神经元标志物 TUJ-1 或星形胶质细胞标志物胶质纤维酸性蛋白的含量。在小鼠中观察到的行为效应与来自磐城市的患者观察到的症状相关。