Cited by 346Neuroendocrine regulation and behaviorSexual Differentiation and DisordersGenetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities

The DOI matches its Crossref record; 131 of the 131 references it cites were found in a registry or an index; 2 of the 25 sources its claims cite were checked for support.

Sexual differentiation of central vasopressin and vasotocin systems in vertebrates: Different mechanisms, similar endpoints

Open access
De Vries, G.J., Panzica, G.C.·2006·Neuroscience

Abstract

Vasopressin neurons in the bed nucleus of the stria terminalis and amygdala and vasotocin neurons in homologous areas in non-mammalian vertebrates show some of the most consistently found neural sex differences, with males having more cells and denser projections than females. These projections have been implicated in social and reproductive behaviors but also in autonomic functions. The sex differences in these projections may cause as well as prevent sex differences in these functions. This paper discusses the anatomy, steroid dependency, and sexual differentiation of these neurons. Although the final steps in sexual differentiation of vasopressin/vasotocin expression may be similar across vertebrate species, what triggers differentiation may vary dramatically. For example, during development, estrogen masculinizes vasopressin expression in rats but feminizes its counterpart in Japanese quail. Apparently, nature consistently finds a way of maintaining sex differences in vasopressin and vasotocin pathways, suggesting that the function of these differences is important enough that it was conserved during evolution.

Overview

AI snapshot

Written from the paper’s full text.

TL;DR

This review argues that central vasopressin/vasotocin pathways in the bed nucleus of the stria terminalis and medial amygdala and their homologs show conserved male-biased sex differences across vertebrates, but the developmental triggers differ. In rats estrogen masculinizes vasopressin expression, whereas in Japanese quail estrogen feminizes the vasotocin counterpart.

Key findings

  • Male-biased AVP/AVT cell number and fiber density in BST/MeA homologs are consistently found across mammals, birds, reptiles, and amphibians; these projections are implicated in social and reproductive behaviors and autonomic functions.
  • Adult AVP/AVT expression is steroid-sensitive: gonadectomy eliminates and hormone replacement reinstates it, but sex differences persist after equal steroid treatment in rats and quail, indicating organizational effects. In rats estrogen masculinizes AVP innervation; in quail estrogen feminizes its AVT counterpart. In prairie voles, testes are essential for masculinization, but testosterone administration to females or neonatally castrated males does not masculinize the system.
  • Sex chromosomal complement contributes independently of gonadal hormones: XY mice had slightly denser AVP innervation than XX mice even when gonadal hormone levels were kept constant.
  • Cellular differentiation likely reflects phenotypic differentiation rather than cell birth/death: AVP cells are born on embryonic days 12 and 13, before hormones trigger sexual differentiation; Bax deletion increased AVP cell number in both sexes but did not eliminate the sex difference; galanin co-expression may determine how many existing cells express AVP.

Methods

  • Narrative comparative review; no new experimental data.
  • Synthesizes published anatomical, steroid-manipulation, tracing, developmental, and genetic studies across vertebrates; Table 1 catalogs studies by species and features such as projections, cell bodies, dimorphism, seasonal/activational effects, organizational effects, and tracing.
  • Main analysis is qualitative synthesis of AVP/AVT expression in BST/MeA and homologs, steroid dependency, and mechanisms of sexual differentiation.

Limitations

  • Stated: the conclusion that BST/MeA are the sources of sexually dimorphic AVP/AVT innervation rests on a limited set of experiments; BST-to-septum evidence is solid, but other BST/MeA projections have not been independently confirmed, and homologous projections in other vertebrates are even less certain, with only a Japanese quail tracing study.
  • Stated: it is unknown whether gonadal steroids act directly on AVP/AVT cells during sexual differentiation; adult rat AVP-ir cells express estrogen receptor alpha, androgen, and progesterone receptors, but developmental receptor expression is unknown, and no study has addressed co-localization in other vertebrates.
  • Stated: molecular and cellular processes mediating hormonal effects on AVP/AVT differentiation remain unidentified, and the functional significance of most CNS sex differences is unknown. Also evident: the review is not systematic and relies on heterogeneous species and assays, so comparative conclusions are qualitative.

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Integrity signals

Registry

Crossref · 10.1016/j.neuroscience.2005.07.050

Cites

131 of 131 references verified0 citation errors · 0 not checkable

Statistics

Nothing to recompute.

Verification

Claims the paper makes

11 No full text of the sources · 5 Own interpretation · 4 No basis given · 3 Sources not found · 3 Not checked yet · 2 Own method · 1 Supported · 1 Partly supported · accuracy not yet measured

Verify all 1 references — free account
  • It may state two separate claims as one. 14
  • Probably not a substantial claim. 4
15 of 15
  • The paper relies on this without support.

    AVP and AVT systems in mammals and non-mammalian vertebrates are homologous.

    “Vasopressin neurons in the bed nucleus of the stria terminalis and amygdala and vasotocin neurons in homologous areas in non-mammalian vertebrates”
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Metadata

Authors
De Vries, G. J., & Panzica, G. C.
Affiliations
University of Turin (IT)
Venue
Neuroscience
Publisher
Elsevier BV
Published
2006-03
Volume
138
Issue
3
Pages
947-955
ISSN
0306-4522 (ISSN-L)
OpenAlex
W1989699697
Cited by
346
References
129
Citations by year
2026: 12 · 2025: 10 · 2024: 10 · 2023: 12 · 2022: 16 · 2021: 25 · 2020: 12 · 2019: 13 · 2018: 16 · 2017: 18 · 2016: 16 · 2015: 16 · 2014: 22 · 2013: 19 · 2012: 19
FWCI
20.61
Type
journal article
Language
en
Open access
Locations
  • Neuroscience (publishedVersion)
  • PubMed (publishedVersion)
  • PubMed Central (submittedVersion)
  • Institutional Research Information System University of Turin (University of Turin) (submittedVersion)
Funders
National Institute of Mental Health (K02-MH01497, R01MH47538, K02 MH001497, R01-MH047538)
Topics
  • Life Sciences › Neuroscience › Endocrine and Autonomic Systems › Neuroendocrine regulation and behavior
  • Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Sexual Differentiation and Disorders
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
Keywords
vasopressin, arginine vasotocin, sexual differentiation, sex differences, bed nucleus of the stria terminalis, amygdala, steroid hormones, estrogen, masculinization, feminization, social behavior, reproductive behavior, autonomic function, non-mammalian vertebrates
MeSH terms
Androgens, Animals, Brain, Coturnix, Estrogens, Female, Humans, Male, Sex Differentiation, Vasopressins, Vasotocin, Vertebrates, Rats

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