Evidence map›Paper›PMID 39211205›Full record

ArticlebioRxiv : the preprint server for biology2025

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 readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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 48019.
Alexis Vega MedinaDepartment of Molecular, Cellular, and Developmental Biology, University of Michigan, Ann Arbor, MI 48019.
Kailynn SchmidtUniversity of New England College of Osteopathic Medicine, Biddeford, ME 04005.
Annie HeDepartment of Molecular, Cellular, and Developmental Biology, University of Michigan, Ann Arbor, MI 48019.
Anna A VankampenDepartment of Molecular, Cellular, and Developmental Biology, University of Michigan, Ann Arbor, MI 48019.
Vinodh BalendranDepartment of Molecular, Cellular, and Developmental Biology, University of Michigan, Ann Arbor, MI 48019.
Sara J AtonDepartment of Molecular, Cellular, and Developmental Biology, University of Michigan, Ann Arbor, MI 48019.

Funding

Linking interneuron-mediated circuit regulation with sleep-dependent plasticity and memory storage in the hippocampusRF1NS118440 · NINDS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI ATON, SARA J · 2020 to 2020
$1.4M
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
NIMH NIH HHS R01 MH135565NINDS NIH HHS R01 NS118440NINDS NIH HHS RF1 NS118440
6 · The paper itself

Abstract

Study objectives: Brief sleep loss alters cognition and synaptic structures of principal neurons in hippocampus and neocortex. However, while Methods: We 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-h period of Results: Dendritic 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. Conclusions: Our 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.

Identifiers

PMID39211205
PMCPMC11360998

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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 OpenQuestion graph.