Evidence map›Paper›PMID 40096531›Full record

ArticleSleep2025

Brief sleep disruption alters synaptic structures among hippocampal and neocortical somatostatin-expressing interneurons.

Frank Raven, Alexis Vega Medina, Kailynn Schmidt, Annie He, Anna A Vankampen, Vinodh Balendran, Sara J Aton

Abstract read
In one paragraph

Article in Sleep, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
–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

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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

9 citing papers in PubMed.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors.

Frank RavenDepartment of Molecular, Cellular, and Developmental Biology, University of Michigan, Ann Arbor, MI, USA.
Alexis Vega MedinaDepartment of Molecular, Cellular, and Developmental Biology, University of Michigan, Ann Arbor, MI, USA.
Kailynn SchmidtUniversity of New England College of Osteopathic Medicine, Biddeford, ME, USA.
Annie HeDepartment of Molecular, Cellular, and Developmental Biology, University of Michigan, Ann Arbor, MI, USA.ORCID 0009-0006-2906-5344
Anna A VankampenDepartment of Molecular, Cellular, and Developmental Biology, University of Michigan, Ann Arbor, MI, USA.ORCID 0009-0008-5219-3541
Vinodh BalendranDepartment of Molecular, Cellular, and Developmental Biology, University of Michigan, Ann Arbor, MI, USA.
Sara J AtonDepartment of Molecular, Cellular, and Developmental Biology, University of Michigan, Ann Arbor, MI, USA.ORCID 0000-0002-2921-0509

Funding

Research Training in BiogerontologyT32AG000114 · NIA · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI SCOTT PLETCHER · 1985 to 2026
$12.4M
CRCNS: Acetylcholine and state-dependent neural network reorganizationR01MH135565 · NIMH · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI ATON, SARA J, ZOCHOWSKI, MICHAL R · 2023 to 2025
$949k
Linking interneuron-mediated circuit regulation with sleep-dependent plasticity and memory storage in the hippocampusR01NS118440 · NINDS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI ATON, SARA J · 2023 to 2024
$880k
NIA NIH HHS T32 AG000114NIH HHS R01NS118440 and R01MH135565NIMH NIH HHS R01 MH135565NINDS NIH HHS R01 NS118440
6 · The paper itself

Abstract

STUDY

objectivesBrief sleep loss alters cognition and synaptic structures of principal neurons in the hippocampus and neocortex. However, while in vivo recording and bioinformatic data suggest that inhibitory interneurons are more strongly affected by sleep loss, it is unclear how sleep and sleep deprivation (SD) affect interneurons' synapses. Disruption of the somatostatin-expressing (SST+) interneuron population seems to be a critical early sign of neuropathology in Alzheimer's dementia, schizophrenia, and bipolar disorder-and the risk of developing all three is increased by habitual sleep loss. We aimed to test how the synaptic structures of SST+ interneurons in various brain regions are affected by brief sleep disruption.

methodsWe used Brainbow 3.0 to label SST+ interneurons in the dorsal hippocampus, prefrontal cortex, and visual cortex of male SST-CRE transgenic mice, then compared synaptic structures in labeled neurons after a 6-hour period of ad lib sleep, or gentle handling SD starting at lights on.

resultsDendritic spine density among SST+ interneurons in both hippocampus and neocortex was altered in a subregion-specific manner, with increased overall and thin spine density in CA1, dramatic increases in spine volume and surface area in CA3, and small but significant changes (primarily decreases) in spine size in CA1, PFC, and V1.

conclusionsWe suggest that the synaptic connectivity of SST+ interneurons is significantly altered in a brain region-specific manner by a few hours of sleep loss. This suggests a cell type-specific mechanism by which sleep loss disrupts cognition and alters excitatory-inhibitory balance in brain networks.

Indexed as

HippocampusInterneuronsNeocortexSleep DeprivationSomatostatinSynapsesAnimalsDendritic SpinesMaleMiceMice, TransgenicSomatostatinexcitatory-inhibitory balancehippocampusinterneuronneocortexsleep deprivationsynaptic plasticitysynaptic structure

Identifiers

PMID40096531
PMCPMC12163128

What Socratic holds

Textmetadata
Read underepoch 390

Registered trials

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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 Socratic graph.