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Extended exposure to tetrabromobisphenol A-bis(2,3-dibromopropyl ether) leads to subfertility in male mice at the late reproductive age.
Li, Yuan-Yuan; Xiong, Yi-Ming; Chen, Xuan-Yue; Sheng, Jia-Yi; Lv, Lin; Li, Xing-Hong; Qin, Zhan-Fen.
Affiliation
  • Li YY; State Key Laboratory of Environmental Chemistry and Ecotoxicology, Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, Haidian District, No. 18, Shuangqing Road, Beijing, 100085, China.
  • Xiong YM; University of Chinese Academy of Sciences, Beijing, 100049, China.
  • Chen XY; State Key Laboratory of Environmental Chemistry and Ecotoxicology, Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, Haidian District, No. 18, Shuangqing Road, Beijing, 100085, China.
  • Sheng JY; University of Chinese Academy of Sciences, Beijing, 100049, China.
  • Lv L; State Key Laboratory of Environmental Chemistry and Ecotoxicology, Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, Haidian District, No. 18, Shuangqing Road, Beijing, 100085, China.
  • Li XH; University of Chinese Academy of Sciences, Beijing, 100049, China.
  • Qin ZF; The High School Affiliated to Renmin, University of China, Beijing, 100080, China.
Arch Toxicol ; 97(11): 2983-2995, 2023 11.
Article in En | MEDLINE | ID: mdl-37606655
ABSTRACT
Tetrabromobisphenol A-bis(2,3-dibromopropyl ether) (TBBPA-BDBPE), a commonly used brominated flame retardant as a decabromodiphenyl ether substitute, has been detected in various environmental compartments, but its health hazards remain largely unknown. Our recent study showed that low-dose exposure of male mice to TBBPA-BDBPE from postnatal day (PND) 0 to 56 caused remarkable damage to the microtubule skeleton in Sertoli cells and the blood-testis barrier (BTB) but exerted little effect on conventional reproductive endpoints in adulthood. To investigate whether TBBPA-BDBPE may cause severe reproductive impairments at late reproductive age, here, we extended exposure of historically administrated male mice to 8-month age and allowed them to mate with non-treated females for the evaluation of fertility, followed by a general examination for the reproductive system. As expected, we found that 8-month exposure to 50 µg/kg/d as well as 1000 µg/kg/d TBBPA-BDBPE caused severe damage to the reproductive system, including reduced sperm counts, increased sperm abnormality, histological alterations of testes. Moreover, microtubule damage and BTB-related impairment were still observed following 8-month exposure. Noticeably, high-dose TBBPA-BDBPE-treated mice had fewer offspring with a female-biased sex ratio. All results show that long-term exposure to TBBPA-BDBPE caused severe reproductive impairment, including poor fertility at late reproductive age. It is therefore concluded that slight testicular injuries in early life can contribute to reproductive impairment at late reproductive age, highlighting that alterations in certain non-conventional endpoints should be noticed as well as conventional endpoints in future reproductive toxicity studies.
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Full text: 1 Database: MEDLINE Main subject: Ether / Infertility Limits: Animals Language: En Year: 2023 Type: Article

Full text: 1 Database: MEDLINE Main subject: Ether / Infertility Limits: Animals Language: En Year: 2023 Type: Article