The Journal of Toxicological Sciences
Toxicogenomics/proteomics Report
siRNA-mediated AMPKα1 subunit gene PRKAA1 silencing enhances methylmercury toxicity in HEK293 cells
Gi-Wook HwangMayumi TobitaTsutomu TakahashiShusuke KugeKayoko KitaAkira Naganuma
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Volume 35 (2010) Issue 4 Pages 601-604

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The environmental pollutant methylmercury is a potent neurotoxin. The mechanisms of toxicity and biological defense remain largely unknown. We found that inhibiting the expression of PRKAA1 (AMPKα1), an activated subunit of AMP-activated protein kinase (AMPK), increased susceptibility of HEK293 cells to methylmercury toxicity. Treatment of the cells with AICAR (5-aminoimidazole-4-carboxamide-1-β-D-ribofuranoside), an AMPK activator, reduced the methylmercury toxicity. Here, we suggest for the first time that the activation (phosphorylation) of AMPK may play an important role in reducing the toxicity of methylmercury.

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© 2010 The Japanese Society of Toxicology
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