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.
引用
收藏
页码:412 / 421
页数:10
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共 10 条
  • [1] Serum Perfluorooctanoate (PFOA) and Perfluorooctane Sulfonate (PFOS) Concentrations and Liver Function Biomarkers in a Population with Elevated PFOA Exposure
    Gallo, Valentina
    Leonardi, Giovanni
    Genser, Bernd
    Lopez-Espinosa, Maria-Jose
    Frisbee, Stephanie J.
    Karlsson, Lee
    Ducatman, Alan M.
    Fletcher, Tony
    [J]. ENVIRONMENTAL HEALTH PERSPECTIVES, 2012, 120 (05) : 655 - 660
  • [2] Perfluorooctane sulfonate (PFOS) and perfluorooctanoate (PFOA) in soils and groundwater of a US metropolitan area: Migration and implications for human exposure
    Xiao, Feng
    Simcik, Matt F.
    Halbach, Thomas R.
    Gulliver, John S.
    [J]. WATER RESEARCH, 2015, 72 : 64 - 74
  • [3] Neonatal exposure to perfluorooctane sulfonate (PFOS) and perfluorooctanoic acid (PFOA) causes neurobehavioural defects in adult mice
    Johansson, N.
    Fredriksson, A.
    Eriksson, P.
    [J]. NEUROTOXICOLOGY, 2008, 29 (01) : 160 - 169
  • [4] PATTERNS OF AGE OF PUBERTY IN RELATION TO EXPOSURE TO PERFLUOROOCTANOIC ACID (PFOA) AND PERFLUOROOCTANE SULFONATE (PFOS) AMONG CHILDREN LIVING IN AN AREA WITH PFOA-CONTAMINATED DRINKING WATER
    Fletcher, T.
    Lopez-Espinosa, M-J
    Armstrong, B.
    Fitz-Simon, N.
    Genser, B.
    Mondal, D.
    [J]. AMERICAN JOURNAL OF EPIDEMIOLOGY, 2011, 173 : S43 - S43
  • [5] In utero exposure to perfluorooctanoate (PFOA) or perfluorooctane sulfonate (PFOS) did not increase body weight or intestinal tumorigenesis in multiple intestinal neoplasia (Min/ plus ) mice
    Ha Thi Ngo
    Hetland, Ragna Bogen
    Sabaredzovic, Azemira
    Haug, Line Smastuen
    Steffensen, Inger-Lise
    [J]. ENVIRONMENTAL RESEARCH, 2014, 132 : 251 - 263
  • [6] Effect of a postnatal high-fat diet exposure on puberty onset, estrous cycle regularity, and kisspeptin expression in female rats
    Lie, Maria E. K.
    Overgaard, Agnete
    Mikkelsen, Jens D.
    [J]. REPRODUCTIVE BIOLOGY, 2013, 13 (04) : 298 - 308
  • [7] Prenatal Alcohol Exposure and Pair Feeding Differentially Impact Puberty and Reproductive Development in Female Rats: Role of the Kisspeptin System
    Sliwowska, Joanna Helena
    Comeau, Wendy L.
    Bodnar, Tamara S.
    Ellis, Linda
    Weinberg, Joanne
    [J]. ALCOHOLISM-CLINICAL AND EXPERIMENTAL RESEARCH, 2016, 40 (11) : 2368 - 2376
  • [8] Arsenic exposure during juvenile and puberty significantly affected reproductive system development of female SD rats
    Chen, Panpan
    Luo, Qiong
    Lin, Yifeng
    Jin, Jiani
    Hu, Kai-Lun
    Wang, Feixia
    Sun, Jiwei
    Chen, Ruixue
    Wei, Juan
    Chen, Guangdi
    Zhang, Dan
    [J]. ECOTOXICOLOGY AND ENVIRONMENTAL SAFETY, 2022, 242
  • [9] Bisphenol A exposure advances puberty onset by changing Kiss1 expression firstly in arcuate nucleus at juvenile period in female rats
    Dong, Wenke
    He, Jingwei
    Wang, Junqi
    Sun, Wen
    Sun, Yanyan
    Yu, Jian
    [J]. REPRODUCTIVE TOXICOLOGY, 2022, 110 : 141 - 149
  • [10] Opposite effects of high- and low-dose di-(2-ethylhexyl) phthalate (DEHP) exposure on puberty onset, oestrous cycle regularity and hypothalamic kisspeptin expression in female rats
    Yu Zhen
    Wang Fan
    Han Junyong
    Lu Rongmei
    Li Qian
    Cai Liangchun
    Li Bishuang
    Chen Jinyan
    Wang Kun
    Lin Wenjin
    Lin Qinghua
    Chen Gang
    Wen Junping
    [J]. REPRODUCTION FERTILITY AND DEVELOPMENT, 2020, 32 (06) : 610 - 618