Evidence map›Paper›PMID 42774051›Full record

ArticleFrontiers in endocrinology2026

Nonlinear and sex-specific effects of V1aR deletion on juvenile social behavior.

D Aspesi, H Vu, I Rivers, M C Stoehr, K L Huhman, H E Albers

Abstract read
In one paragraph

Article in Frontiers in endocrinology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

Who cites it

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

D AspesiNeuroscience Institute and Center for Behavioral Neuroscience, Georgia State University, Atlanta, GA, United States.
H VuNeuroscience Institute and Center for Behavioral Neuroscience, Georgia State University, Atlanta, GA, United States.
I RiversNeuroscience Institute and Center for Behavioral Neuroscience, Georgia State University, Atlanta, GA, United States.
M C StoehrNeuroscience Institute and Center for Behavioral Neuroscience, Georgia State University, Atlanta, GA, United States.
K L HuhmanNeuroscience Institute and Center for Behavioral Neuroscience, Georgia State University, Atlanta, GA, United States.
H E AlbersNeuroscience Institute and Center for Behavioral Neuroscience, Georgia State University, Atlanta, GA, United States.

Funding

Advances in the Study of Social NeuroendocrinologyR21MH109302 · NIMH · GEORGIA STATE UNIVERSITY · PI ALBERS, H. ELLIOTT, HUHMAN, KIM L · 2016 to 2017
$417k
NIMH NIH HHS R21 MH109302
6 · The paper itself

Abstract

Introduction: Social behaviors emerge during juvenile development and require the integration of social motivation, recognition, and context-appropriate responses. Arginine vasopressin signaling through the V1a receptor (V1aR) has been implicated in multiple aspects of social behavior, yet its role across distinct behavioral domains, developmental stages, and sexes remains poorly understood. Methods: We used a CRISPR/Cas9-generated V1aR knockout model in Syrian hamsters to examine the effects of V1aR disruption on social interaction, social recognition, and social avoidance in juvenile males and females. Hamsters were tested during the peripubertal period (postnatal days 35-36), prior to the onset of stable estrous cyclicity in females. Results: In a dyadic social interaction assay, V1aR deletion increased social investigation, particularly anogenital investigation, in knockout animals, whereas heterozygous males exhibited reduced locomotor activity and increased self-directed behaviors. In a social odor recognition task, heterozygous animals failed to discriminate between familiar and novel conspecific odors at a 20-min interval, while wild-type and knockout animals showed intact recognition. No odor discrimination or genotype-dependent differences were observed at a 24-h interval, indicating limited evidence of long-term retention across groups. Following social defeat, heterozygous males displayed increased social avoidance, spending less time near an aggressor and more time in the avoidance zone compared with other groups. Discussion: Together, these findings reveal domain-specific and nonlinear effects of V1aR disruption on juvenile social behavior, with heterozygous animals exhibiting the most pronounced alterations. These results suggest that V1aR contributes to social behavior in a nonlinear, genotype-dependent, and context-dependent manner and highlight the importance of developmental stage and sex in shaping vasopressin-dependent social processes.

Indexed as

Behavior, AnimalReceptors, VasopressinSocial BehaviorAnimalsArginine VasopressinCricetinaeFemaleMaleMesocricetusArginine VasopressinReceptors, Vasopressinarginine vasopressinsex differencessocial avoidancesocial interactionsocial recognitionSyrian hamster

Identifiers

PMID42774051
PMCPMC13593422

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.