Cited by 99Neuroendocrine regulation and behaviorNeuropeptides and Animal PhysiologyNeurotransmitter Receptor Influence on Behavior

Relationships among estrogen receptor, oxytocin and vasopressin gene expression and social interaction in male mice

Murakami, G., Hunter, R. G., Fontaine, C., Ribeiro, A., Pfaff, D.·2011·European Journal of Neuroscience

Abstract

The incidence of social disorders such as autism and schizophrenia is significantly higher in males, and the presentation more severe, than in females. This suggests the possible contribution of sex hormones to the development of these psychiatric disorders. There is also evidence that these disorders are highly heritable. To contribute toward our understanding of the mechanisms underlying social behaviors, particularly social interaction, we assessed the relationship of social interaction with gene expression for two neuropeptides, oxytocin (OT) and arginine vasopressin (AVP), using adult male mice. Social interaction was positively correlated with: oxytocin receptor (OTR) and vasopressin receptor (V1aR) mRNA expression in the medial amygdala; and OT and AVP mRNA expression in the paraventricular nucleus of the hypothalamus (PVN). When mice representing extremes of social interaction were compared, all of these mRNAs were more highly expressed in high social interaction mice than in low social interaction mice. OTR and V1aR mRNAs were highly correlated with estrogen receptor α (ERα) mRNA in the medial amygdala, and OT and AVP mRNAs with estrogen receptor β (ERβ) mRNA in the PVN, indicating that OT and AVP systems are tightly regulated by estrogen receptors. A significant difference in the level of ERα mRNA in the medial amygdala between high and low social interaction mice was also observed. These results support the hypothesis that variations of estrogen receptor levels are…

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Crossref · 10.1111/j.1460-9568.2011.07761.x

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  • In the PVN, AVP mRNA expression is altered by experimental manipulations that impact agonistic and affiliative interactions, including play.

    “In the PVN, AVP mRNA expression is altered by experimental manipulations that impact agonistic and affiliative interactions, including play (Veenema et al., 2006; Veenema and Neumann, 2009; Murakami et al., 2011; De Souza et al., 2013).”

    From Sexually dimorphic role for vasopressin in the development of social play (2014) · cites this paper as Murakami et al., 2011

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Authors
Murakami, G., Hunter, R. G., Fontaine, C., Ribeiro, A., & Pfaff, D.
Affiliations
Rockefeller University (US)
Corresponding author
Murakami, G.
Venue
European Journal of Neuroscience
Publisher
Wiley
Published
2011-07-12
Volume
34
Issue
3
Pages
469-477
ISSN
0953-816X (ISSN-L)
OpenAlex
W1939470521
Cited by
99
References
14
Citations by year
2025: 3 · 2024: 6 · 2023: 5 · 2022: 5 · 2021: 6 · 2020: 6 · 2019: 3 · 2018: 10 · 2017: 10 · 2016: 8 · 2015: 8 · 2014: 12 · 2013: 7 · 2012: 7
FWCI
12.62
Type
journal article
Language
en
Open access
closed
Locations
  • European Journal of Neuroscience (publishedVersion)
  • PubMed (publishedVersion)
Funders
  • National Institutes of Health
  • Eunice Kennedy Shriver National Institute of Child Health and Human Development (R37HD005751, HD05751)
Topics
  • Social Sciences › Psychology › Social Psychology › Neuroendocrine regulation and behavior
  • Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuropeptides and Animal Physiology
  • Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neurotransmitter Receptor Influence on Behavior
Keywords
social interaction, oxytocin, vasopressin, estrogen receptor alpha, estrogen receptor beta, oxytocin receptor, vasopressin V1a receptor, medial amygdala, paraventricular nucleus, sex differences in social behavior, autism spectrum disorder, schizophrenia, sex hormones, gene expression, mice
MeSH terms
Animals, Arginine Vasopressin, Behavior, Animal, Mental Disorders, Female, Interpersonal Relations, Male, Mice, Inbred C57BL, Neuropsychological Tests, Oxytocin, Paraventricular Hypothalamic Nucleus, Social Behavior, Gene Expression, Receptors, Vasopressin, Receptors, Oxytocin, Estrogen Receptor alpha, Estrogen Receptor beta, Mice

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