Susceptibility of metallothionein-null mice to the behavioral alterations caused by exposure to mercury vapor at human-relevant concentration

被引:31
|
作者
Yoshida, M
Watanabe, C
Satoh, M
Yasutake, A
Sawada, M
Ohtsuka, Y
Akama, Y
Tohyama, C
机构
[1] Univ Tokyo, Grad Sch Med, Sch Int Hlth, Dept Human Ecol,Bunkyo Ku, Tokyo 1130033, Japan
[2] St Marianna Univ, Sch Med, Dept Biochem, Div Chem,Miyamae Ku, Kawasaki, Kanagawa 2618511, Japan
[3] Gifu Pharmaceut Univ, Dept Hygien, Gifu 5028585, Japan
[4] Natl Inst Minamata Dis, Biochem Sect, Kumamoto 8670008, Japan
[5] Tottori Univ, Dept Vet Pathol, Tottori 6800945, Japan
[6] Meisei Univ, Dept Chem, Tokyo 1910041, Japan
[7] Natl Inst Environm Studies, Environm Hlth Sci Div, Tsukuba, Ibaraki 3050053, Japan
关键词
mercury (elemental); low-level exposure; metallothionein; knock-out mouse; behavior; learning;
D O I
10.1093/toxsci/kfh138
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
While recent human studies suggested adverse neurobehavioral outcomes of low-level exposure to mercury vapor (Hg-0) as found among those having dental amalgam fillings and dental personnel, past animal experiments only dealt with exposure at much higher mercury concentrations. The present study aimed to examine neurobehavioral effects of prolonged, low-level Hg-0 exposure in mice and to evaluate the protective role of metallothionein-I,II (MT-I,II) against Hg-0-induced neurotoxicity, using a knock-out strain of mice. Adult female metallothionein-I,II-null (MT-null) and wild-type OLA129/C57BL6 mice were exposed to 0.06 mg/m(3) of Hg-0 for 8 h per day for 23 weeks. Neurobehavioral effects were evaluated at 12 and 23 weeks of exposure using open-field test and passive avoidance test. Subcellular distribution of mercury and the induction of MT were also assessed. The Hg-0 exposure resulted in significantly enhanced locomotion in the open-field test and poorer performance in the passive avoidance test at a brain Hg concentration less than 1 ppm. These effects were slightly exaggerated in MT-null mice, which showed less induction of MT, lower brain Hg concentration, and lower calculated concentration of MT-unbound cytosolic Hg. The results showed, for the first time, that a concentration of Hg-0 relevant to human exposure level could cause neurobehavioral effects in adult mice. The higher susceptibility of MT-null mice suggested that MT-I,II have protective roles in the metal-induced neurobehavioral toxicity, which cannot be entirely explained by kinetic mechanisms, thus suggesting an involvement of nonkinetic mechanisms.
引用
收藏
页码:69 / 73
页数:5
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