共 10 条
Neonatal and juvenile exposure to perfluorooctanoate (PFOA) and perfluorooctane sulfonate (PFOS): Advance puberty onset and kisspeptin system disturbance in female rats
被引:50
|作者:
Du, Guizhen
[1
,2
,3
]
Hu, Jialei
[4
]
Huang, Zhenyao
[1
,2
]
Yu, Mingming
[1
,2
]
Lu, Chuncheng
[1
,2
,3
]
Wang, Xinru
[1
,2
,3
]
Wu, Di
[1
,2
,3
]
机构:
[1] Nanjing Med Univ, State Key Lab Reprod Med, Inst Toxicol, Nanjing 211166, Jiangsu, Peoples R China
[2] Nanjing Med Univ, Sch Publ Hlth, Key Lab Modern Toxicol, Minist Educ, Nanjing 211166, Jiangsu, Peoples R China
[3] Nanjing Med Univ, Sch Publ Hlth, Ctr Global Hlth, Nanjing, Jiangsu, Peoples R China
[4] Jiangsu Prov Ctr Dis Control & Prevent, Nanjing 210009, Jiangsu, Peoples R China
基金:
中国国家自然科学基金;
关键词:
PFOA;
PFOS;
Puberty;
Kisspeptin/GPR54;
Hypothalamus;
PERFLUOROALKYL ACIDS;
GLOBAL DISTRIBUTION;
ETHINYL ESTRADIOL;
MESSENGER-RNA;
ER-BETA;
HORMONE;
REPRODUCTION;
NEURONS;
BRAIN;
ACTIVATION;
D O I:
10.1016/j.ecoenv.2018.10.025
中图分类号:
X [环境科学、安全科学];
学科分类号:
08 ;
0830 ;
摘要:
Perfluorooctanoate (PFOA) and perfluorooctane sulfonate (PFOS) are widespread and persistent chemicals in the environment, and limited data about their effects on puberty development are available. In order to explore the effects of neonatal and juvenile PFOA/PFOS exposure on puberty maturation, female rats were injected with PFOA or PFOS at 0.1, 1 and 10 mg/kg/day during postnatal day (PND) 1-5 or 26-30. The day of vaginal opening (VO) and first estrus were significantly advanced in 10 mg/kg PFOA, 1 and 10 mg/kg PFOS groups after neonatal and juvenile exposure. Besides, neonatal PFOA/PFOS exposure increased body weight and anogenital distance (AGD) in a non-dose-dependent manner. Estradiol and luteinizing hormone levels were also increased with more frequent occurrences of irregular estrous cycles in 0.1 and 1 mg/kg PFOA/PFOS exposure groups. Although no altered ovarian morphology was observed, follicles numbers were reduced in neonatal groups. Kiss1, Kiss1r and ER alpha mRNA expressions were downregulated after two periods' exposure in the hypothalamic anteroventral periventricular (AVPV) and arcuate (ARC) nuclei. PFOA/PFOS exposure also suppressed kisspeptin fiber intensities, especially at the high dose. In conclusion, neonatal and juvenile are critical exposure periods, during which puberty maturation may be vulnerable to environmental exposure of PFOA/PFOS, and kisspeptin system plays a key role during these processes.
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页码:412 / 421
页数:10
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