Bisphenol A Activates the Nrf1/2-Antioxidant Response Element Pathway in HEK 293 Cells

作者:Chepelev Nikolai L; Enikanolaiye Mutiat I; Chepelev Leonid L; Almohaisen Abdulrahman; Chen QiXuan; Scoggan Kylie A; Coughlan Melanie C; Cao Xu Liang; Jin Xiaolei; Willmore William G*
来源:Chemical Research in Toxicology, 2013, 26(3): 498-506.
DOI:10.1021/tx400036v

摘要

Bisphenol A (BPA) is used in the production of polycarbonate plastics and epoxy resins for baby bottles, liners of canned food, and many other consumer products. Previously, BPA has been shown to reduce the activity of several antioxidant enzymes, which may contribute to oxidative stress. However, the underlying mechanism of the BPA-mediated effect upon antioxidant enzyme activity is unknown. Antioxidant and phase II metabolizing enzymes protect cells from oxidative stress and are transcriptionally activated by Nrf1 and Nrf2 factors through their cis-regulatory antioxidant response elements (AREs). In this work, we have assessed the effect of BPA on the Nrf1/2-ARE pathway in cultured human embryonic kidney (HEK) 293 cells. Surprisingly, glutathione and reactive oxygen species (ROS) assays revealed that BPA application created a more reduced intracellular environment in cultured HEK 293 cells. Furthermore, BPA increased the transactivation activity of ectopic Nrf1 and Nrf2 and increased the expression of ARE-target genes ho-1 and nqo1 at high (100-200 mu M) BPA concentrations only. Our study suggests that BPA activates the Nrf1/2-ARE pathway at high (%26gt;10 mu M) micromolar concentrations.

  • 出版日期2013-3