Activation of ornithine decarboxylase protects against methylmercury toxicity by increasing putrescine

Masayuki Sato, Takashi Toyama, Jin Yong Lee, Nobuhiko Miura, Akira Naganuma, Gi Wook Hwang

Research output: Contribution to journalArticle

3 Citations (Scopus)

Abstract

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 methylmercury 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.

Original languageEnglish
Pages (from-to)120-126
Number of pages7
JournalToxicology and Applied Pharmacology
Volume356
DOIs
Publication statusPublished - 2018 Oct 1

Keywords

  • Methylmercury
  • Ornithine Decarboxylase
  • Putrescine

ASJC Scopus subject areas

  • Toxicology
  • Pharmacology

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