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Article

Hepatic and Nephric NRF2 Pathway Up-Regulation, an Early Antioxidant Response, in Acute Arsenic-Exposed Mice

1
Department of Occupational and Environmental Health, School of Public Health, China Medical University, Shenyang 110013, China
2
Cao County Center for Disease Control and Prevention, Heze 274400, China
3
Environment and Non-Communicable Diseases Research Center, School of Public Health, China Medical University, Shenyang 110013, China
*
Author to whom correspondence should be addressed.
Academic Editor: Paul B. Tchounwou
Int. J. Environ. Res. Public Health 2015, 12(10), 12628-12642; https://doi.org/10.3390/ijerph121012628
Received: 27 July 2015 / Revised: 28 September 2015 / Accepted: 6 October 2015 / Published: 12 October 2015
Inorganic arsenic (iAs), a proven human carcinogen, damages biological systems through multiple mechanisms, one of them being reactive oxygen species (ROS) production. NRF2 is a redox-sensitive transcription factor that positively regulates the genes of encoding antioxidant and detoxification enzymes to neutralize ROS. Although NRF2 pathway activation by iAs has been reported in various cell types, however, the experimental data in vivo are very limited and not fully elucidated in humans. The present investigation aimed to explore the hepatic and nephric NRF2 pathway upregulation in acute arsenic-exposed mice in vivo. Our results showed 10 mg/kg NaAsO2 elevated the NRF2 protein and increased the transcription of Nrf2 mRNA, as well as up-regulated NRF2 downstream targets HO-1, GST and GCLC time- and dose-dependently both in the liver and kidney. Acute NaAsO2 exposure also resulted in obvious imbalance of oxidative redox status represented by the increase of GSH and MDA, and the decrease of T-AOC. The present investigation reveals that hepatic and nephric NRF2 pathway expression is an early antioxidant defensive response upon iAs exposure. A better knowledge about the NRF2 pathway involvment in the cellular response against arsenic could help improve the strategies for reducing the cellular toxicity related to this metalloid. View Full-Text
Keywords: arsenic; ROS; NRF2; liver; kidney arsenic; ROS; NRF2; liver; kidney
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MDPI and ACS Style

Li, J.; Duan, X.; Dong, D.; Zhang, Y.; Li, W.; Zhao, L.; Nie, H.; Sun, G.; Li, B. Hepatic and Nephric NRF2 Pathway Up-Regulation, an Early Antioxidant Response, in Acute Arsenic-Exposed Mice. Int. J. Environ. Res. Public Health 2015, 12, 12628-12642. https://doi.org/10.3390/ijerph121012628

AMA Style

Li J, Duan X, Dong D, Zhang Y, Li W, Zhao L, Nie H, Sun G, Li B. Hepatic and Nephric NRF2 Pathway Up-Regulation, an Early Antioxidant Response, in Acute Arsenic-Exposed Mice. International Journal of Environmental Research and Public Health. 2015; 12(10):12628-12642. https://doi.org/10.3390/ijerph121012628

Chicago/Turabian Style

Li, Jinlong, Xiaoxu Duan, Dandan Dong, Yang Zhang, Wei Li, Lu Zhao, Huifang Nie, Guifan Sun, and Bing Li. 2015. "Hepatic and Nephric NRF2 Pathway Up-Regulation, an Early Antioxidant Response, in Acute Arsenic-Exposed Mice" International Journal of Environmental Research and Public Health 12, no. 10: 12628-12642. https://doi.org/10.3390/ijerph121012628

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