Evidence map›Paper›PMID 35618950›Full record

ArticleNature neuroscience2022

Adolescent sleep shapes social novelty preference in mice.

Wen-Jie Bian, Chelsie L Brewer, Julie A Kauer, Luis de Lecea

Open access · greenAbstract read
In one paragraph

Article in Nature neuroscience, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 54 papers.

0numbers the graph read from it
0cells of the map it votes in
54citing papers in PubMed
10.8field-weighted citation impact, top 1% of its field
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

54 citing papers in PubMed, 94 citations in OpenAlex.

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  11. Adolescent Chronic Sleep Disruption Increases Blood-Brain Barrier Permeability, but in a Time-, Region- and Sex-Dependent Manner in CD-1 Mice.International journal of developmental neuroscience : the official journal of the International Society for Developmental Neuroscience · 2025
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors at 1 institution in 1 country.

Wen-Jie BianDepartment of Psychiatry and Behavioral Sciences, Stanford University School of Medicine, Stanford, CA, USA. wjbian@stanford.edu.ORCID http://orcid.org/0000-0002-0426-1297
Chelsie L BrewerDepartment of Psychiatry and Behavioral Sciences, Stanford University School of Medicine, Stanford, CA, USA.ORCID http://orcid.org/0000-0002-0089-2411
Julie A KauerDepartment of Psychiatry and Behavioral Sciences, Stanford University School of Medicine, Stanford, CA, USA.ORCID http://orcid.org/0000-0002-3362-1642
Luis de LeceaDepartment of Psychiatry and Behavioral Sciences, Stanford University School of Medicine, Stanford, CA, USA. llecea@stanford.edu.ORCID http://orcid.org/0000-0002-8921-5942
Neurosciences Institute · US

Funding

Interdisciplinary Research Training in Pain and Substance Use DisordersT32DA035165 · NIDA · STANFORD UNIVERSITY · PI SEAN C MACKEY · 2013 to 2026
$7.2M
Inhibitory Synaptic Transmission, Stress and Drugs of AbuseR01DA011289 · NIDA · STANFORD UNIVERSITY · PI KAUER, JULIE A. · 1997 to 2023
$6.8M
VECTOR COREP30NS069375 · NINDS · STANFORD UNIVERSITY · PI ALCUDIA, JAVIER · 2011 to 2019
$6.3M
Optogenetic Control of Vigilance State TransitionR01MH087592 · NIMH · STANFORD UNIVERSITY · PI DE LECEA, LUIS · 2010 to 2017
$3.2M
Functional Heterogeneity of Hypocretin NeuronsR01MH116470 · NIMH · STANFORD UNIVERSITY · PI APPELBAUM, LIOR YOSEF, DE LECEA, LUIS · 2019 to 2023
$2.4M
Optogenetic interrogation of sleep circuits during agingR01AG047671 · NIA · STANFORD UNIVERSITY · PI DE LECEA, LUIS, WYSS-CORAY, TONY · 2014 to 2018
$2.1M
Neuronal mapping of anxiety and panicR01MH102638 · NIMH · STANFORD UNIVERSITY · PI DE LECEA, LUIS · 2014 to 2018
$2.0M
Arousal circuitry and opiate-associated memoriesR01HL150566 · NHLBI · STANFORD UNIVERSITY · PI CHEN, XIAOKE, DE LECEA, LUIS · 2019 to 2019
$1.6M
Inflammatory injury-mediated synaptic plasticity in the periaqueductal grayF32NS123008 · NINDS · STANFORD UNIVERSITY · PI BREWER, CHELSIE L · 2021 to 2022
$110k
NHLBI NIH HHS R01 HL150566NIA NIH HHS R01 AG047671NIDA NIH HHS R01 DA011289NIDA NIH HHS T32 DA035165NIMH NIH HHS R01 MH087592NIMH NIH HHS R01 MH102638NIMH NIH HHS R01 MH116470NINDS NIH HHS F32 NS123008NINDS NIH HHS P30 NS069375
6 · The paper itself

Abstract

Sleep disturbances frequently occur in neurodevelopmental disorders such as autism, but the developmental role of sleep is largely unexplored, and a causal relationship between developmental sleep defects and behavioral consequences in adulthood remains elusive. Here, we show that in mice, sleep disruption (SD) in adolescence, but not in adulthood, causes long-lasting impairment in social novelty preference. Furthermore, adolescent SD alters the activation and release patterns of dopaminergic neurons in the ventral tegmental area (VTA) in response to social novelty. This developmental sleep function is mediated by balanced VTA activity during adolescence; chemogenetic excitation mimics, whereas silencing rescues, the social deficits of adolescent SD. Finally, we show that in Shank3-mutant mice, improving sleep or rectifying VTA activity during adolescence ameliorates adult social deficits. Together, our results identify a critical role of sleep and dopaminergic activity in the development of social interaction behavior.

Indexed as

Dopaminergic NeuronsVentral Tegmental AreaAnimalsDopamineMiceMicrofilament ProteinsNerve Tissue ProteinsSleepSocial BehaviorDopamineMicrofilament ProteinsNerve Tissue ProteinsShank3 protein, mouse

Identifiers

PMID35618950
PMCPMC9283223
OpenAlexW4281550473

What OpenQuestion holds

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LicenceTDM
Read underepoch 390

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.