Evidence map›Paper›PMID 37928499›Full record

ArticleFrontiers in sleep2023

Regulation of dendritic spines in the amygdala following sleep deprivation.

Lindsay Rexrode, Matthew Tennin, Jobin Babu, Caleb Young, Ratna Bollavarapu, Lamiorkor Ameley Lawson, Jake Valeri, Harry Pantazopoulos, Barbara Gisabella

Open access · diamondAbstract read
In one paragraph

Article in Frontiers in sleep, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
1.9field-weighted citation impact, top 15% 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

8 citing papers in PubMed, 1 synthesis or guideline pooled it, 11 citations in OpenAlex.

  1. Pooled it
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  5. 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

9 authors at 2 institutions in 1 country.

Lindsay RexrodeDepartment of Psychiatry and Human Behavior, University of Mississippi Medical Center, Jackson, MS, United States.
Matthew TenninDepartment of Psychiatry and Human Behavior, University of Mississippi Medical Center, Jackson, MS, United States.
Jobin BabuDepartment of Psychiatry and Human Behavior, University of Mississippi Medical Center, Jackson, MS, United States.
Caleb YoungDepartment of Psychiatry and Human Behavior, University of Mississippi Medical Center, Jackson, MS, United States.
Ratna BollavarapuDepartment of Psychiatry and Human Behavior, University of Mississippi Medical Center, Jackson, MS, United States.
Lamiorkor Ameley LawsonDepartment of Psychiatry and Human Behavior, University of Mississippi Medical Center, Jackson, MS, United States.
Jake ValeriDepartment of Psychiatry and Human Behavior, University of Mississippi Medical Center, Jackson, MS, United States.
Harry PantazopoulosDepartment of Psychiatry and Human Behavior, University of Mississippi Medical Center, Jackson, MS, United States.
Barbara GisabellaDepartment of Psychiatry and Human Behavior, University of Mississippi Medical Center, Jackson, MS, United States.
University of Mississippi Medical Center · USJackson Memorial Hospital · US

Funding

Morphological Correlates of Memory Consolidation During SleepR21MH117460 · NIMH · UNIVERSITY OF MISSISSIPPI MED CTR · PI GISABELLA, BARBARA · 2019 to 2020
$441k
NIMH NIH HHS R21 MH117460
6 · The paper itself

Abstract

The amygdala is a hub of emotional circuits involved in the regulation of cognitive and emotional behaviors and its critically involved in emotional reactivity, stress regulation, and fear memory. Growing evidence suggests that the amygdala plays a key role in the consolidation of emotional memories during sleep. Neuroimaging studies demonstrated that the amygdala is selectively and highly activated during rapid eye movement sleep (REM) and sleep deprivation induces emotional instability and dysregulation of the emotional learning process. Regulation of dendritic spines during sleep represents a morphological correlate of memory consolidation. Several studies indicate that dendritic spines are remodeled during sleep, with evidence for broad synaptic downscaling and selective synaptic upscaling in several cortical areas and the hippocampus. Currently, there is a lack of information regarding the regulation of dendritic spines in the amygdala during sleep. In the present work, we investigated the effect of 5 h of sleep deprivation on dendritic spines in the mouse amygdala. Our data demonstrate that sleep deprivation results in differential dendritic spine changes depending on both the amygdala subregions and the morphological subtypes of dendritic spines. We observed decreased density of mushroom spines in the basolateral amygdala of sleep deprived mice, together with increased neck length and decreased surface area and volume. In contrast, we observed greater densities of stubby spines in sleep deprived mice in the central amygdala, indicating that downscaling selectively occurs in this spine type. Greater neck diameters for thin spines in the lateral and basolateral nuclei of sleep deprived mice, and decreases in surface area and volume for mushroom spines in the basolateral amygdala compared to increases in the cental amygdala provide further support for spine type-selective synaptic downscaling in these areas during sleep. Our findings suggest that sleep promotes synaptic upscaling of mushroom spines in the basolateral amygdala, and downscaling of selective spine types in the lateral and central amygdala. In addition, we observed decreased density of phosphorylated cofilin immunoreactive and growth hormone immunoreactive cells in the amygdala of sleep deprived mice, providing further support for upscaling of dendritic spines during sleep. Overall, our findings point to region-and spine type-specific changes in dendritic spines during sleep in the amygdala, which may contribute to consolidation of emotional memories during sleep.

Indexed as

amygdaladendritic spinesgrowth hormonememory consolidationsleep

Identifiers

PMID37928499
PMCPMC10624159
OpenAlexW4362586506

What OpenQuestion holds

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LicenceCC BY
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 OpenQuestion graph.