ToxSci Advance Access published online on August 28, 2007
Toxicological Sciences, doi:10.1093/toxsci/kfm221
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Elemental selenium at nano size (Nano-Se) as a potential chemopreventive agent with reduced risk of selenium toxicity: comparison with Se-methylselenocysteine in mice
University of Science and Technology of China, Hefei 230052, Anhui, PR China
* Corresponding author. School of Chemistry and Material Science, University of Science and Technology of China, Southern Campus, Meiling Avenue No.121, Hefei, 230052, Anhui, P.R.China. Tel: +86 551 3492386, Fax: +86 551 3492386. E-mail address: zjszyzzc{at}mail.hf.ah.cn
Received April 5, 2007; revision received June 29, 2007; accepted August 6, 2007
| Abstract |
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As an essential trace element with a narrow margin between beneficial and toxic effects and as a promising chemopreventive agent needed to be consumed for a long term, the toxicity of selenium is always a crucial concern. Based on the clinical findings and the recent studies in selenoprotein gene-modified mice, it is likely that the antioxidant function of one or more selenoproteins is responsible for the chemopreventive effect. Furthermore, upregulation of phase 2 enzymes by selenium has frequently been the focus of chemopreventive mechanism at supranutritional dietary levels. Se-methylselenocysteine (SeMSC), a nature-occurring organic selenium product, is considered as one of the most effective chemopreventive selenocompounds. Present study revealed, as compared with SeMSC, elemental selenium at nano size (Nano-Se) possessed equal efficacy in increasing the activities of glutathione peroxidase, thioredoxin reductase and glutathione S-transferase but had much lower toxicity as indicated by median lethal dose, acute liver injury, survival rate and short-term toxicity. Our results suggest Nano-Se can serve as a potential chemopreventive agent with reduced risk of selenium toxicity.
Key Words: Nano-Se; Se-methylselenocysteine; Toxicity; Bioavailability; Selenoenzymes; Glutathione S-transferase.