Cited by 60Sexual Differentiation and DisordersEstrogen and related hormone effectsNeuroendocrine regulation and behavior

Estrogenic regulation of social behavior and sexually dimorphic brain formation

Ogawa, Sonoko, Tsukahara, Shinji, Choleris, Elena, Vasudevan, Nandini·2020·Neuroscience & Biobehavioral Reviews

Abstract

It has long been known that the estrogen, 17β-estradiol (17β-E), plays a central role for female reproductive physiology and behavior. Numerous studies have established the neurochemical and molecular basis of estrogenic induction of female sexual behavior, i.e., lordosis, in animal models. In addition, 17β-E also regulates male-type sexual and aggressive behavior. In males, testosterone secreted from the testes is irreversibly aromatized to 17β-E in the brain. We discuss the contribution of two nuclear receptor isoforms, estrogen receptor (ER)α and ERβ to the estrogenic regulation of sexually dimorphic brain formation and sex-typical expression of these social behaviors. Furthermore, 17β-E is a key player for social behaviors such as social investigation, preference, recognition and memory as well as anxiety-related behaviors in social contexts. Recent studies also demonstrated that not only nuclear receptor-mediated genomic signaling but also membrane receptor-mediated non-genomic actions of 17β-E may underlie the regulation of these behaviors. Finally, we will discuss how rapidly developing research tools and ideas allow us to investigate estrogenic action by emphasizing behavioral neural networks.

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Crossref · 10.1016/j.neubiorev.2018.10.012

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5 of 5 references verified0 citation errors · 0 not checkable

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  • Estrogens play a fundamental role in the sexually dimorphic formation of brain structures by modulating neural circuits that control sex-specific behavior, including social interaction.

    “Indeed, estrogens play a fundamental role in the sexually dimorphic formation of brain structures by modulating neural circuits that control sex-specific behavior, including social interaction (Ogawa et al., 2020).”

    From Oxytocin neurons mediate the effect of social isolation via the VTA circuits (2022) · cites this paper as Ogawa et al., 2020

  • In the brain there are sex differences in tissue structures and dimorphic nuclei exhibiting morphological sex differences are considered as the structural basis for generating sex differences in brain functions.

    “In the brain there are sex differences in the tissue structures and the dimorphic nuclei exhibiting morphological sex differences are considered as the structural basis for generating sex differences in brain functions (Ogawa et al., 2020).”

    From Oxytocin neurons mediate the effect of social isolation via the VTA circuits (2022) · cites this paper as Ogawa et al., 2020

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Authors
Ogawa, S., Tsukahara, S., Choleris, E., & Vasudevan, N.
Affiliations
  • University of Tsukuba (JP)
  • Saitama University (JP)
  • University of Guelph (CA)
  • University of Reading (GB)
Corresponding author
Ogawa, Sonoko
Venue
Neuroscience & Biobehavioral Reviews
Publisher
Elsevier BV
Published
2020-03
Volume
110
Pages
46-59
ISSN
0149-7634 (ISSN-L)
OpenAlex
W2898613973
Cited by
60
References
5
Citations by year
2026: 4 · 2025: 7 · 2024: 18 · 2023: 5 · 2022: 10 · 2021: 8 · 2020: 5 · 2019: 3
FWCI
0.39
Type
journal article
Language
en
Open access
closed
Locations
  • Neuroscience & Biobehavioral Reviews (publishedVersion)
  • PubMed (publishedVersion)
  • CentAUR (University of Reading) (acceptedVersion)
Funders
  • JSPS (15H05724, 17H05549)
  • ST (17K08567)
  • NSERC Discovery (400212)
  • NSF CAREER (IOS-1053716)
  • University of Reading startup fund to NV
Topics
  • 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
  • Social Sciences › Psychology › Social Psychology › Neuroendocrine regulation and behavior
Keywords
estradiol, estrogen receptor alpha, estrogen receptor beta, social behavior, lordosis, male aggression, social investigation, social recognition memory, anxiety, non-genomic estrogen signaling, membrane estrogen receptor, nuclear receptor signaling
MeSH terms
Animals, Estrogens, Humans, Memory, Sexual Behavior, Sexual Behavior, Animal, Social Behavior, Recognition, Psychology

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