Evidence map›Paper›PMID 31550501›Full record

ArticleBrain, behavior, and immunity2020

Sexually dimorphic role of BNST vasopressin cells in sickness and social behavior in male and female mice.

Jack Whylings, Nicole Rigney, Nicole V Peters, Geert J de Vries, Aras Petrulis

Abstract read
In one paragraph

Article in Brain, behavior, and immunity, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

26 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. The Anterior BNST Is Required for Novelty-Driven Social Interaction.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2026
    Article
  3. A sexually dimorphic neuronal cluster in the mouse medial amygdala responds to male sexual status.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  4. Article
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  6. Article
  7. A vasopressin circuit that modulates mouse social investigation and anxiety-like behavior in a sex-specific manner.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Review
  14. Sex Differences in Social Cognition.Current topics in behavioral neurosciences · 2023
    Review
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Jack WhylingsNeuroscience Institute, Georgia State University, 100 Piedmont Ave SE, Atlanta, GA 30303, USA. Electronic address: jwhylings1@student.gsu.edu.
Nicole RigneyNeuroscience Institute, Georgia State University, 100 Piedmont Ave SE, Atlanta, GA 30303, USA. Electronic address: nrigney1@student.gsu.edu.
Nicole V PetersNeuroscience Institute, Georgia State University, 100 Piedmont Ave SE, Atlanta, GA 30303, USA.
Geert J de VriesNeuroscience Institute, Georgia State University, 100 Piedmont Ave SE, Atlanta, GA 30303, USA; Department of Biology, Georgia State University, 100 Piedmont Ave SE, Atlanta, GA 30303, USA. Electronic address: devries@gsu.edu.
Aras PetrulisNeuroscience Institute, Georgia State University, 100 Piedmont Ave SE, Atlanta, GA 30303, USA. Electronic address: apetrulis@gsu.edu.

Funding

Sex Differences in the Neural Control of Social Behavior; SupplementR01MH121603 · NIMH · GEORGIA STATE UNIVERSITY · PI DE VRIES, GEERT J., PETRULIS, ARAS T · 2020 to 2024
$2.0M
The Neuropeptide Architecture of Social CommunicationR21MH111104 · NIMH · GEORGIA STATE UNIVERSITY · PI DE VRIES, GEERT J., PETRULIS, ARAS T · 2016 to 2017
$417k
NIMH NIH HHS R01 MH121603NIMH NIH HHS R21 MH111104
6 · The paper itself

Abstract

Circumstantial evidence supports the hypothesis that the sexually dimorphic vasopressin (AVP) innervation of the brain tempers sickness behavior in males. Here we test this hypothesis directly, by comparing sickness behavior in animals with or without ablations of BNST AVP cells, a major source of sexually dimorphic AVP in the brain. We treated male and female AVP-iCre+ and AVP-iCre- mice that had been injected with viral Cre-dependent caspase-3 executioner construct into the BNST with lipopolysaccharide (LPS) or sterile saline, followed by behavioral analysis. In all groups, LPS treatment reliably reduced motor behavior, increased anxiety-related behavior, and reduced sucrose preference and consumption. Male mice, whose BNST AVP cells had been ablated (AVP-iCre+), displayed only minor reductions in LPS-induced sickness behavior, whereas their female counterparts displayed, if anything, an increase in sickness behaviors. All saline-treated mice with BNST AVP cell ablations consumed more sucrose than did control mice, and males, but not females, with BNST AVP cell ablations showed reduced preference for novel conspecifics compared to control mice. These data confirm that BNST AVP cells control social behavior in a sexually dimorphic way, but do not play a critical role in altering sickness behavior.

Indexed as

Sex CharacteristicsSocial BehaviorAnimalsArginine VasopressinBrainEatingFemaleMaleMiceSucroseArginine VasopressinSucroseArginine vasopressinBed nucleus of the stria terminalisSickness behaviorSocial behavior

Identifiers

PMID31550501
PMCPMC6906230

What OpenQuestion holds

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Registered trials

None linked

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.