4-Bromodiphenyl ether delays pubertal Leydig cell development in rats

被引:25
作者
Chen, Xianwu [1 ,2 ]
Dong, Yaoyao [2 ,3 ]
Tian, Erpo [5 ]
Xie, Lubin [1 ,2 ]
Wang, Guimin [2 ,4 ]
Li, Xiaoheng [2 ,4 ]
Chen, Xiuxiu [1 ,2 ]
Chen, Yong [2 ,4 ]
Lv, Yao [2 ,3 ]
Ni, Chaobo [2 ,4 ]
Fang, Yinghui [2 ,3 ]
Zhong, Ying [5 ]
Ge, Ren-Shan [1 ,2 ,4 ]
机构
[1] Wenzhou Med Univ, Affiliated Hosp 2, Dept Obstet & Gynecol, Wenzhou 325027, Zhejiang, Peoples R China
[2] Wenzhou Med Univ, Yuying Childrens Hosp, Wenzhou 325027, Zhejiang, Peoples R China
[3] Wenzhou Med Univ, Affiliated Hosp 2, Dept Pharm, Wenzhou 325027, Zhejiang, Peoples R China
[4] Wenzhou Med Univ, Affiliated Hosp 2, Dept Anesthesiol, Wenzhou 325027, Zhejiang, Peoples R China
[5] Jinjiang Matern & Child Hlth Hosp, Chengdu 610000, Sichuan, Peoples R China
关键词
4-Bromodiphenyl ether; Leydig cell; Sertoli cell; Leydig cell development; Testosterone; POLYBROMINATED DIPHENYL ETHERS; ACTIVATED PROTEIN-KINASE; GLUCOSE-HOMEOSTASIS; STEROIDOGENESIS; TESTIS; APOPTOSIS; RECEPTOR; EXPOSURE; MOUSE; GENE;
D O I
10.1016/j.chemosphere.2018.08.008
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Polybrominated diphenyl ethers are a class of brominated flame retardants that are potential endocrine disruptors. 4-Bromodiphenyl ether (BDE-3) is the most abundant photodegradation product of higher polybrominated diphenyl ethers. However, whether BDE-3 affects Leydig cell development during puberty is still unknown. The objective of this study was to explore effects of BDE-3 on the pubertal development of rat Leydig cells. Male Sprague Dawley rats (35 days of age) were gavaged daily with BDE-3 (0, 50, 100, and 200 mg/kg body weight/day) for 21 days. BDE-3 decreased serum testosterone levels (1.099 +/- 0.412 ng/ml at a dose of 200 mg/kg BDE-3 when compared to the control level (2.402 +/- 0.184 ng/ml, mean +/- S.E.). BDE-3 decreased Leydig cell size and cytoplasmic size at a dose of 200 mg/kg, decreased Lhcgr, Star, Dhh, and Sox9 mRNA levels at >= 100 mg/kg and Scarb1, Cyp11a1, Hsd17b3, and Fshr at 200 mg/kg. BED-3 also decreased the phosphorylation of AKT1, AKT2, ERK1/2, and AMPK at 100 or 200 mg/kg. BDE-3 in vitro induced ROS generation, inhibited androgen production, down-regulated Lhcgr, Scarb1, Star, Cyp11a1, Hsd3b1, Srd5a1, and Akr1c14 expression in immature Leydig cells after 24-h treatment. In conclusion, the current study indicates that BDE-3 disrupts Leydig cell development via suppressing AKT, ERK1/2, and AMPK phosphorylation and inducing ROS generation. (C) 2018 Elsevier Ltd. All rights reserved.
引用
收藏
页码:986 / 997
页数:12
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