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Tissue distribution and endocrine disruption effects of chronic exposure to pharmaceuticals and personal care products mixture at environmentally relevant concentrations in zebrafish
被引:19
|作者:
Hamid, Naima
[1
,2
,3
]
Junaid, Muhammad
[4
]
Manzoor, Rakia
[3
,5
]
Duan, Jin-Jing
[1
]
Lv, Ming
[4
]
Xu, Nan
[4
]
Pei, De-Sheng
[1
]
机构:
[1] Chongqing Med Univ, Sch Publ Hlth & Management, Chongqing 400016, Peoples R China
[2] Chinese Acad Sci, Chongqing Inst Green & Intelligent Technol, Chongqing 400714, Peoples R China
[3] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
[4] Peking Univ, Sch Environm & Energy, Shenzhen Grad Sch, Key Lab Heavy Met Pollut Control & Reutilizat, Shenzhen 518055, Peoples R China
[5] Chinese Acad Sci, Inst Genet & Dev Biol, State Key Lab Mol Dev Biol, Beijing 100101, Peoples R China
基金:
中国国家自然科学基金;
关键词:
PPCPs toxicity;
Xenoestrogens;
HPG axis;
Estrogen receptors;
Molecular docking;
DANIO-RERIO;
POTENTIAL MECHANISMS;
MOLECULAR DOCKING;
TOXICITY;
FISH;
FATE;
DICLOFENAC;
IBUPROFEN;
WATER;
REPRODUCTION;
D O I:
10.1016/j.aquatox.2021.106040
中图分类号:
Q17 [水生生物学];
学科分类号:
071004 ;
摘要:
Pharmaceuticals and personal care products (PPCPs) as emerging contaminants are ubiquitously present in the aquatic environment. Using in vivo and in silico techniques, this study aims to elucidate tissue distribution and endocrine disruption effects of chronic exposure (120 days) to PPCP mixture at environmentally relevant concentrations (ERCs) in adult zebrafish. Results from UHPLC-MS/MS analyses showed elevated distribution of PPCPs in zebrafish tissues in the order of liver > gonad > brain. Upregulation of steroid hormone receptors, both gonadotropin, and steroidogenic genes perturb the HPG axis pathway in females, while male fish exhibited significantly downregulated expressions of vtg, cyp17, and 17 beta hsd genes with inhibited fecundity. The Spearman correlation indicated a significant positive relationship between PPCPs bioaccumulation and mRNA levels of HPG axis genes. In silico molecular docking (MD) revealed specific amino acid residues of PPCPs binding with zebrafish estrogen receptors. Furthermore, the strongest binding energies of sulfamethoxazole, carbamazepine, and triclosan were discovered in er alpha and er beta estrogen receptors, confirming PPCPs' xenoestrogenic behavior. To summarize, chronic exposure to ERCs resulted in a high accumulation of PPCPs in the liver and gonad tissues of adult zebrafish, as well as associated perturbed genetic responses. As a result, strict environmental regulations for the disposal of PPCPs should be ensured to protect ecological and public health.
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页数:11
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