Sexual differentiation of the vertebrate nervous system
Abstract
Understanding the mechanisms that give rise to sex differences in the behavior of nonhuman animals may contribute to the understanding of sex differences in humans. In vertebrate model systems, a single factor-the steroid hormone testosterone-accounts for most, and perhaps all, of the known sex differences in neural structure and behavior. Here we review some of the events triggered by testosterone that masculinize the developing and adult nervous system, promote male behaviors and suppress female behaviors. Testosterone often sculpts the developing nervous system by inhibiting or exacerbating cell death and/or by modulating the formation and elimination of synapses. Experience, too, can interact with testosterone to enhance or diminish its effects on the central nervous system. However, more work is needed to uncover the particular cells and specific genes on which testosterone acts to initiate these events.
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If the brain is exposed to testosterone either from its own testes in males or from an exogenous source in females, it will be masculinized.
“If the brain is exposed to testosterone either from its own testes in males or from an exogenous source in females, it will be masculinized [59–64].”
From Sex differences in metabolic homeostasis, diabetes, and obesity (2015) · cites this paper as [62]
Classically, the organizational effects of fetal sex steroids were produced during time-limited critical periods to shape enduring differences in male and female brain structure and function.
“Classically, the organizational effects of fetal sex steroids were produced during time-limited critical periods to shape enduring differences in male and female brain structure and function (Morris et al., 2004).”
From Sex-specific developmental alterations in DYRK1A expression in the brain of a Down syndrome mouse model (2024) · cites this paper as Morris et al., 2004
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“Classically, the organizational effects of fetal sex steroids were produced during time-limited critical periods to shape enduring differences in male and female brain structure and function (Morris et al., 2004).”
- Authors
- Morris, J. A., Jordan, C. L., & Breedlove, S. M.
- Affiliations
- Michigan State University (US)
- Corresponding author
- Breedlove, S Marc
- ORCID
- Breedlove, S Marc
- Venue
- Nature Neuroscience
- Published
- 2004-09-27
- Volume
- 7
- Issue
- 10
- Pages
- 1034-1039
- ISSN
- 1097-6256 (ISSN-L)
- 1546-1726
- OpenAlex
- W2011700227
- Cited by
- 627
- References
- 5
- Citations by year
- 2026: 6 · 2025: 14 · 2024: 19 · 2023: 25 · 2022: 24 · 2021: 27 · 2020: 23 · 2019: 14 · 2018: 24 · 2017: 39 · 2016: 34 · 2015: 32 · 2014: 32 · 2013: 42 · 2012: 27
- FWCI
- 1.73
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature Neuroscience (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Sexual Differentiation and Disorders
- Social Sciences › Psychology › Social Psychology › Neuroendocrine regulation and behavior
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Keywords
- testosterone, sex differences in behavior, masculinization, neural development, synaptic pruning, cell death, experience-dependent plasticity
- MeSH terms
- Animals, Central Nervous System, Humans, Neural Pathways, Neuronal Plasticity, Receptors, Androgen, Sex Differentiation, Testosterone, Vertebrates, Gene Expression Regulation, Developmental
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