Vasopressin V1b receptor knockout reduces aggressive behavior in male mice
Abstract
Increased aggression is commonly associated with many neurological and psychiatric disorders. Current treatments are largely empirical and are often accompanied by severe side effects, underscoring the need for a better understanding of the neural bases of aggression. Vasopressin, acting through its 1a receptor subtype, is known to affect aggressive behaviors. The vasopressin 1b receptor (V1bR) is also expressed in the brain, but has received much less attention due to a lack of specific drugs. Here we report that mice without the V1bR exhibit markedly reduced aggression and modestly impaired social recognition. By contrast, they perform normally in all the other behaviors that we have examined, such as sexual behavior, suggesting that reduced aggression and social memory are not simply the result of a global deficit in sensorimotor function or motivation. Fos-mapping within chemosensory responsive regions suggests that the behavioral deficits in V1bR knockout mice are not due to defects in detection and transmission of chemosensory signals to the brain. We suggest that V1bR antagonists could prove useful for treating aggressive behavior seen, for example, in dementias and traumatic brain injuries.
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Unconditional deletion of Avpr1b impairs social recognition memory.
“unconditional deletion of this gene impairs social recognition memory22,23.”
From The hippocampal CA2 region is essential for social memory (2014) · cites this paper as [22]
Avpr1b mRNA is also expressed outside hippocampus, and its deletion results in changes in non-hippocampal dependent behaviors, including reduced aggression and decreased sociability.
“However, Avpr1b mRNA is also expressed outside hippocampus21 and its deletion results in changes in non-hippocampal dependent behaviors, including reduced aggression and decreased sociability22,23”
From The hippocampal CA2 region is essential for social memory (2014) · cites this paper as [22]
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References 51 · Cited by 397
- Authors
- Wersinger, S. R., Ginns, E. I., O'Carroll, A.-M., Lolait, S. J., & Young III, W. S.
- Affiliations
- National Institutes of Health (US)
- University of Massachusetts Chan Medical School (US)
- University of Bristol (GB)
- ORCID
- Lolait, S J
- Venue
- Molecular Psychiatry
- Published
- 2002-10-01
- Volume
- 7
- Issue
- 9
- Pages
- 975-984
- ISSN
- 1359-4184 (ISSN-L)
- 1476-5578
- OpenAlex
- W2119147856
- Cited by
- 397
- References
- 51
- Citations by year
- 2026: 4 · 2025: 8 · 2024: 12 · 2023: 15 · 2022: 9 · 2021: 23 · 2020: 16 · 2019: 13 · 2018: 24 · 2017: 21 · 2016: 20 · 2015: 19 · 2014: 20 · 2013: 14 · 2012: 20
- FWCI
- 21.65
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Molecular Psychiatry (publishedVersion)
- PubMed (publishedVersion)
- eScholarship@UMassChan (submittedVersion)
- Explore Bristol Research (submittedVersion)
- Funders
- National Institutes of Health
- Topics
- Social Sciences › Psychology › Social Psychology › Neuroendocrine regulation and behavior
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neurotransmitter Receptor Influence on Behavior
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuropeptides and Animal Physiology
- Keywords
- vasopressin V1b receptor, aggression, knockout mice, social recognition, social memory, chemosensory processing, vasopressin receptor antagonists, traumatic brain injury, dementia, sexual behavior
- MeSH terms
- Age Factors, Aggression, Animals, Behavior, Animal, Body Temperature, Brain Chemistry, Corticosterone, Eating, Exploratory Behavior, Female, Male, Mice, Inbred C57BL, Motor Activity, Neurons, Phenotype, Sexual Behavior, Animal, Stress, Physiological, Testosterone, Visual Perception, Proto-Oncogene Proteins c-fos, Receptors, Vasopressin, Mice, Knockout, Maze Learning, Recognition, Psychology, Mice
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