Abstract |
4-Bromodiphenyl ether (BDE3) is a photodegradation product of higher polybrominated diphenyl ether flame retardants and is known as an endocrine disruptor. However, it is unclear whether and how BDE3 affects the development of fetal testes. This study aimed to investigate the effect of in utero exposure to BDE3 on fetal testicular development in rats. From gestational day (GD) 12-21, BDE3 (0, 50, 100, and 200 mg/kg) was daily gavaged to female pregnant Sprague Dawley rats. BDE3 significantly reduced serum testosterone levels of male pups starting at 50 mg/kg. BDE3 reduced fetal Leydig cell number at a dose of 200 mg/kg without affecting fetal Leydig cell cluster frequency and Sertoli cell number. In addition, BDE3 down-regulated the expression of fetal Leydig cell genes ( Cyp11a1, Hsd3b1, Cyp17a1, and Hsd17b3) and their proteins at 100 and/or 200 mg/kg. RNA-seq analysis showed that genes responsive to cAMP (Ass1, Gpd1, Rpl13a) were down-regulated and hypoxia-related genes (Egln3 and P4ha1) were up-regulated at 200 mg/kg. In utero exposure to BDE3 can promote autophagy and apoptosis of fetal Leydig cells via increasing the levels of Beclin1, LC3-II, BAX, and by decreasing the levels of p62 and BCL2. In conclusion, in utero exposure to BDE3 blocks the development of fetal rat testes.
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Authors | Yang Li, Feifei Ma, Zengqiang Li, Yige Yu, Haoni Yan, Anam Tahir, Wenwen Zheng, Xiaoheng Li, Tongliang Huang, Ren-Shan Ge |
Journal | Toxicology letters
(Toxicol Lett)
Vol. 342
Pg. 38-49
(May 15 2021)
ISSN: 1879-3169 [Electronic] Netherlands |
PMID | 33582287
(Publication Type: Journal Article)
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Copyright | Copyright © 2021 Elsevier B.V. All rights reserved. |
Chemical References |
- 4-bromodiphenyl ether
- Halogenated Diphenyl Ethers
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Topics |
- Animals
- Apoptosis
(drug effects)
- Autophagy
(drug effects)
- Dose-Response Relationship, Drug
- Female
- Fetal Development
(drug effects)
- Fetus
(drug effects)
- Gene Expression Regulation, Developmental
(drug effects)
- Halogenated Diphenyl Ethers
(administration & dosage, toxicity)
- Male
- Pregnancy
- Rats
- Rats, Sprague-Dawley
- Sequence Analysis, RNA
- Signal Transduction
(drug effects)
- Testis
(drug effects, embryology)
- Transcriptome
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