Cited by 195Effects and risks of endocrine disrupting chemicalsSexual Differentiation and DisordersEstrogen and related hormone effects

Neonatal genistein or bisphenol-A exposure alters sexual differentiation of the AVPV

Patisaul, Heather B., Fortino, Anne E., Polston, Eva K.·2006·Neurotoxicology and Teratology

Abstract

There is growing concern that naturally occurring and chemically manufactured endocrine-active compounds (EACs) may disrupt hormone-dependent events during central nervous system development. We examined whether postnatal exposure to the phytoestrogen genistein (GEN) or the plastics component bisphenol-A (BIS) affected sexual differentiation of the anteroventral periventricular nucleus of the hypothalamus (AVPV) in rats. The AVPV is sexually differentiated in rodents. The female AVPV is larger than the male AVPV and contains a higher number of cells expressing tyrosine hydroxylase (TH). Sexual differentiation of the AVPV results from exposure of the male nervous system to estrogen aromatized from testicular testosterone secreted in the first few days after birth. Thus, we hypothesized that exposure to EACs during this critical period could alter the sexually dimorphic expression of TH and the overall expression of estrogen receptor alpha (ERalpha) in the AVPV. Animals were given 4 subcutaneous injections of sesame oil (control), 50 microg 17beta-estradiol (E2), 250 microg GEN, or 250 microg BIS at 12-h intervals over postnatal days (PND) 1 and 2 and sacrificed on PND 19. E2 treatment masculinized TH immunoreactivity (TH-ir) in the female AVPV while exposure to GEN or BIS demasculinized TH-ir in the male AVPV. In addition, we identified a population of neurons co-expressing TH and ERalpha located primarily in the medial region of the AVPV. Normally, females have nearly three t…

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Crossref · 10.1016/j.ntt.2005.11.004

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  • Neonatal treatment with BPA reduces sex differences in the brain and can modify neurite and dendrite formation in rodents.

    “Neonatal treatment with BPA in general reduces sex differences in the brain and can modify neurite and dendrite formation [3], [8], [9], [10], [11].”

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Authors
Patisaul, H. B., Fortino, A. E., & Polston, E. K.
Corresponding author
Polston, Eva K.
Venue
Neurotoxicology and Teratology
Publisher
Elsevier BV
Published
2006-01
Volume
28
Issue
1
Pages
111-118
ISSN
0892-0362 (ISSN-L)
OpenAlex
W2003316529
Cited by
195
References
2
Citations by year
2026: 3 · 2025: 1 · 2024: 4 · 2023: 3 · 2022: 3 · 2021: 13 · 2020: 7 · 2019: 9 · 2018: 13 · 2017: 8 · 2016: 13 · 2015: 11 · 2014: 12 · 2013: 18 · 2012: 12
FWCI
9.63
Type
journal article
Language
en
Open access
closed
Locations
  • Neurotoxicology and Teratology (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Physical Sciences › Environmental Science › Health, Toxicology and Mutagenesis › Effects and risks of endocrine disrupting chemicals
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Sexual Differentiation and Disorders
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Estrogen and related hormone effects
Keywords
genistein, bisphenol A, endocrine active compounds, sexual differentiation, anteroventral periventricular nucleus, hypothalamus, tyrosine hydroxylase, estrogen receptor alpha, aromatization, estradiol, developmental neurotoxicity, sex differences, phytoestrogens, plastics
MeSH terms
Bisphenol A Compounds, Animals, Animals, Newborn, Benzhydryl Compounds, Cell Count, Cell Differentiation, Disease Models, Animal, Estradiol, Estrogens, Non-Steroidal, Female, Growth Inhibitors, Male, Nervous System Malformations, Phenols, Pregnancy, Preoptic Area, Sex Characteristics, Sex Differentiation, Tyrosine 3-Monooxygenase, Rats, Sprague-Dawley, Genistein, Estradiol Congeners, Estrogen Receptor alpha, Rats

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