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Sex-specific thyroid disruption caused by phenanthrene in adult zebrafish (Danio rerio).

Authors :
Zhong, Liqiao
Wu, Luyin
Ru, Huijun
Wei, Nian
Yao, Fan
Zhang, He
Ni, Zhaohui
Duan, Xinbin
Li, Yunfeng
Source :
Comparative Biochemistry & Physiology Part C: Toxicology & Pharmacology. Jan2023, Vol. 263, pN.PAG-N.PAG. 1p.
Publication Year :
2023

Abstract

Polycyclic aromatic hydrocarbons (PAHs) are well-known contaminants with widespread distribution in environment and food. Phenanthrene is one of the most abundant PAHs in food and aquatic environment and generates reproductive and developmental toxicity in zebrafish. Nonetheless, whether phenanthrene caused sex-specific thyroid disruption in adult zebrafish is unclear. To determine this, adult zebrafish (male and female) were treated with phenanthrene (0, 0.85, 8.5, and 85 μg/L) for 60 days. After the treatment period, we assessed the concentrations of thyroid hormones (THs) and expression levels of genes in the hypothalamic-pituitary-thyroid (HPT) axis. The results showed that phenanthrene exposure can lead to thyroid disruption in both male and female zebrafish. Exposure to phenanthrene dramatically reduced the levels of L-thyroxine (T4) and L-triiodothyronine (T3) in both male and female zebrafish, with a similar trend in both. However, the genes expression profiles of hypothalamic-pituitary-thyroid (HPT) axis were sex-specific. In all, the present study demonstrated that phenanthrene exposure could result in sex-specific thyroid disruption in adult zebrafish. [Display omitted] • Phenanthrene exposure caused thyroid disruption in both male and female zebrafish. • Phenanthrene exposure deduced thyroid hormones regardless of gender. • The genes expression profiles of HPT axis were sex-specific after phenanthrene exposure. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
15320456
Volume :
263
Database :
Academic Search Index
Journal :
Comparative Biochemistry & Physiology Part C: Toxicology & Pharmacology
Publication Type :
Academic Journal
Accession number :
160253092
Full Text :
https://doi.org/10.1016/j.cbpc.2022.109484