The nucleus accumbens to ventral pallidum pathway regulates social play behavior via sex-specific mechanisms in juvenile rats.

Jessica D A Lee, Daniela N Anderson, Isabella C Orsucci, Samantha M Bowden, Alexa H Veenema

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Article in Brain structure & function, 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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5 · Who and what money

Authors and funding

5 authors.

Jessica D A LeeNeurobiology of Social Behavior Laboratory, Department of Psychology, Michigan State University, East Lansing, MI, 48824, USA. jlee33@kumc.edu.

Daniela N AndersonNeurobiology of Social Behavior Laboratory, Department of Psychology, Michigan State University, East Lansing, MI, 48824, USA.

Isabella C OrsucciNeurobiology of Social Behavior Laboratory, Department of Psychology, Michigan State University, East Lansing, MI, 48824, USA.

Samantha M BowdenNeurobiology of Social Behavior Laboratory, Department of Psychology, Michigan State University, East Lansing, MI, 48824, USA.

Alexa H VeenemaNeurobiology of Social Behavior Laboratory, Department of Psychology and Neuroscience Program, Michigan State University, East Lansing, MI, 48824, USA. aveenema@msu.edu.

Funding

Oxytocin neural circuitry involvement in juvenile social playR01MH125806 · NIMH · MICHIGAN STATE UNIVERSITY · PI Alexandra H. Veenema · 2022 to 2026

$1.9M

National science foundation GRFP DGE-1848739NIH HHS R01MH125806

6 · The paper itself

Abstract

Social play behavior is a rewarding behavior predominantly displayed by juveniles of various mammalian species, including humans and rats. Although the mesolimbic reward system is involved in the regulation of social play, how brain regions in this system interact to regulate social play behavior is unknown. Here, we determined the involvement of the ventral pallidum (VP) as well as inputs from the nucleus accumbens (NAc) to the VP in the regulation of social play in male and female juvenile rats. We show that acute pharmacological inactivation of the VP, via microinfusion of the GABA-A receptor agonist muscimol, decreased social play behaviors in both sexes. Next, using Gad1-iCre rats, we show that chemogenetic stimulation of NAcGABA terminals in the VP decreased VP neuronal activation and decreased social play behaviors in both sexes. These findings together indicate that reduced inhibitory NAc input to the VP permits activation of the VP which facilitates the expression of social play behaviors. Lastly, we show that the equal expression of social play behavior in males and females is associated with a male-specific decrease in fos activation of NAc shell neurons projecting to the VP. This sex-specific change in NAc shell activation following social play exposure eliminated a baseline sex difference in NAc shell activation. In conclusion, these findings may support a model in which the sex-specific modulation of NAc shell inhibitory input to the VP facilitates activation of the VP that is necessary for the typical and equal expression of social play behavior in male and female juvenile rats.

Indexed as

Basal ForebrainNucleus AccumbensPlay and PlaythingsSex CharacteristicsSocial BehaviorAnimalsFemaleGABA-A Receptor AgonistsGlutamate DecarboxylaseMaleMuscimolNeural PathwaysNeuronsProto-Oncogene Proteins c-fosRatsRats, TransgenicGABA-A Receptor AgonistsGlutamate Decarboxylaseglutamate decarboxylase 1MuscimolProto-Oncogene Proteins c-fosChemogeneticsJuvenilesNucleus accumbensRatsSex differencesSocial playVentral pallidum

Identifiers

PMID41973241

DOI10.1007/s00429-026-03100-0

PMCPMC13076443

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LicenceCC BY

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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.