Fluorene-9-bisphenol exposure induces cytotoxicity in mouse oocytes and causes ovarian damage

被引:40
|
作者
Jia, Zhenzhen [1 ,4 ]
Wang, Hongyu [1 ]
Feng, Zeyang [2 ]
Zhang, Shaozhi [1 ]
Wang, Lining [1 ]
Zhang, Jingwen [1 ]
Liu, Qianqian [1 ]
Zhao, Xin [2 ]
Feng, Daofu [3 ]
Feng, Xizeng [1 ]
机构
[1] Nankai Univ, Minist Educ, State Key Lab Med Chem Biol, Coll Life Sci,Key Lab Bioact Mat, Tianjin 300071, Peoples R China
[2] Nankai Univ, Inst Robot & Automat Informat Syst, Tianjin 300071, Peoples R China
[3] Tianjin Med Univ, Gen Hosp, Dept Gen Surg, 154 Anshan Rd, Tianjin 300052, Peoples R China
[4] Shandong Normal Univ, Shandong Prov Key Lab Anim Resistance Biol, Key Lab Food Nutr & Safety, Coll Life Sci,Inst Biomed Sci, Jinan 250014, Shandong, Peoples R China
关键词
Endocrine-disrupting chemicals; BHPF; Oocyte maturation; Oxidative stress; Ovary damage; EARLY-EMBRYO DEVELOPMENT; OXIDATIVE STRESS; BISPHENOL-A; IN-VITRO; INDUCED APOPTOSIS; REACTIVE OXYGEN; ZONA-PELLUCIDA; DNA; FERTILIZATION; MATURATION;
D O I
10.1016/j.ecoenv.2019.05.019
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Fluorene-9-bisphenol (BHPF), a substitute for bisphenol A, is a chemical component of plastics for industrial production. There is evidence that BHPF exerts an antioestrogenic effect on mice, induces endometrial atrophy and leads to adverse pregnancy outcomes. However, the effects of BHPF on oocyte maturation and ovary development as well as its possible mechanisms remain unclear. The objective of this study was to investigate the toxicity and mechanism of BHPF exposure in mouse oocytes in vitro and in vivo. Our results showed that BHPF could inhibit the maturation of oocytes in vitro by reducing the protein level of p-MAPK and destroying the meiotic spindle. We found that in vitro, BHPF-treated oocytes showed increased ROS levels, DNA damage, mitochondria) dysfunction, and expression of apoptosis- and autophagy-related genes, such as Bax, cleaved-caspase 3, LC 3 and Atg 12. In addition, in vivo experiments showed that BHPF exposure could induce the expression of oxidative stress genes (Cat, Gpx 3 and Sod 2) and apoptosis genes (Bax, Bcl-2 and Cleaved-caspase 3) and increase the number of atresia follicles in the ovaries. Our data showed that BHPF exposure affected the first polar body extrusion of oocytes, increased oxidative stress, destroyed spindle assembly, caused DNA damage, altered mitochondrial membrane potentials, induced apoptosis and autophagy, and affected ovarian development.
引用
收藏
页码:168 / 178
页数:11
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