Activation of ornithine decarboxylase protects against methylmercury toxicity by increasing putrescine

被引:7
作者
Sato, Masayuki [1 ]
Toyama, Takashi [1 ]
Lee, Jin-Yong [1 ,2 ]
Miura, Nobuhiko [3 ]
Naganuma, Akira [1 ]
Hwang, Gi-Wook [1 ]
机构
[1] Tohoku Univ, Grad Sch Pharmaceut Sci, Lab Mol & Biochem Toxicol, Sendai, Miyagi 9808578, Japan
[2] Aichi Gakuin Univ, Sch Pharm, Lab Pharmaceut Hlth Sci, Chikusa Ku, 1-100 Kusumoto Cho, Nagoya, Aichi 4648650, Japan
[3] Japan Natl Inst Occupat Safety & Hlth, Div Hlth Effects Res, Tama Ku, 6-21-1 Nagao, Kawasaki, Kanagawa 2148585, Japan
关键词
Methylmercury; Ornithine Decarboxylase; Putrescine; MATERNAL FISH CONSUMPTION; OXIDATIVE STRESS; POLYAMINES; EXPOSURE; MERCURY; NEUROTOXICITY; BIOCHEMISTRY; EXPRESSION; SPERMINE; OXIDASE;
D O I
10.1016/j.taap.2018.08.002
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
We previously reported significantly increased level of putrescine, a polyamine, in the brains of mice administered methylmercury. Moreover, addition of putrescine to culture medium reduced methylmercury toxicity in C17.2 mouse neural stem cells. In this study, the role of ornithine decarboxylase (ODC), an enzyme involved in putrescine synthesis, in response to methylmercury toxicity was investigated. Methylmercury increased ODC activity in mouse cerebrum and cerebellum, but this increase was hardly observed in the kidney and liver, where methylmercury accumulated at a high concentration. In the cerebrum and cerebellum, increased putrescine was observed with methylmercury administration. Methylmercury increased ODC activity in C17.2 cells, but this was almost completely abolished in the presence of an ODC inhibitor. Methylmercury also increased the level of ODC protein in mouse brain and C17.2 cells. In addition, C17.2 cells pretreated with ODC inhibitor showed higher methylmercury sensitivity than control cells. These results suggest that the increased ODC activity by methyl mercury is involved in the increase in putrescine level, and ODC plays an important role in the reduction of methylmercury toxicity. This is the first study to provide evidence that increased ODC activity may be a protective response against methylmercury-induced neurotoxicity.
引用
收藏
页码:120 / 126
页数:7
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