Effects of deletion of the transcription factor Nrf2 and benzo [a]pyrene treatment on ovarian follicles and ovarian surface epithelial cells in mice

被引:35
|
作者
Lim, Jinhwan [1 ]
Ortiz, Laura [1 ]
Nakamura, Brooke N. [1 ]
Hoang, Yvonne D. [1 ]
Banuelos, Jesus [1 ]
Flores, Victoria N. [1 ]
Chan, Jefferson Y. [3 ]
Luderer, Ulrike [1 ,2 ]
机构
[1] Univ Calif Irvine, Dept Med, Irvine, CA 92717 USA
[2] Univ Calif Irvine, Dept Dev & Cell Biol, Irvine, CA 92717 USA
[3] Univ Calif Irvine, Dept Pathol & Lab Med, Irvine, CA 92717 USA
关键词
NRF2; Ovarian aging; Benzo[a]pyrene; Oxidative stress; Polycyclic aromatic hydrocarbon; DNA adduct; POLYCYCLIC AROMATIC-HYDROCARBONS; MICROSOMAL EPOXIDE HYDROLASE; REACTIVE OXYGEN; GENE-EXPRESSION; OXIDATIVE STRESS; GONADOTROPIN REGULATION; METABOLIC-ACTIVATION; HYDROXYLASE-ACTIVITY; TARGETED DISRUPTION; CIGARETTE-SMOKING;
D O I
10.1016/j.reprotox.2015.07.080
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Polycyclic aromatic hydrocarbons, like benzo[a]pyrene (BaP), are ubiquitous environmental pollutants and potent ovarian toxicants. The transcription factor NRF2 is an important regulator of the cellular response to electrophilic toxicants like BaP and to oxidative stress. NRF2 regulates transcription of genes involved in the detoxification of reactive metabolites of BaP and reactive oxygen species. We therefore hypothesized that Nrf2-/- mice have accelerated ovarian aging and increased sensitivity to the ovarian toxicity of BaP. A single injection of BaP dose-dependently depleted ovarian follicles in Nrf2+/+ and Nrf2-/- mice, but the effects of BaP were not enhanced in the absence of Nrf2. Similarly, Nrf2-/- mice did not have increased ovarian BaP DNA adduct formation compared to Nrf2+/+ mice. Ovarian follicle numbers did not differ between peripubertal Nrf2-/- and Nrf2+/+ mice, but by middle age, Nrf2-/- mice had significantly fewer primordial follicles than Nrf2-/- mice, consistent with accelerated ovarian aging. (C) 2015 Elsevier Inc. All rights reserved.
引用
收藏
页码:24 / 32
页数:9
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