Evidence map›Paper›PMID 38157434›Full record

ArticleAnesthesiology2024

Anatomical Substrates of Rapid Eye Movement Sleep Rebound in a Rodent Model of Post-sevoflurane Sleep Disruption.

Navya Atluri, Elzbieta Dulko, Michal Jedrusiak, Joanna Klos, Hari P Osuru, Eric Davis, Mark Beenhakker, Jaideep Kapur, Zhiyi Zuo, Nadia Lunardi

Open access · greenAbstract read
In one paragraph

Article in Anesthesiology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.2field-weighted citation impact, top 47% 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

2 citing papers in PubMed, 1 citations in OpenAlex.

  1. Article
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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

10 authors at 2 institutions in 2 countries.

Navya AtluriDepartment of Anesthesiology, University of Virginia, Charlottesville, Virginia.
Elzbieta DulkoNeuroscience Graduate Program, University of Virginia, Charlottesville, Virginia.
Michal JedrusiakDepartment of Anesthesiology, University of Virginia, Charlottesville, Virginia.
Joanna KlosDepartment of Synapses-Circuits-Plasticity, Max Planck Institute for Biological Intelligence, Munich, Germany.ORCID 0000-0002-6365-4226
Hari P OsuruDepartment of Anesthesiology, University of Virginia, Charlottesville, Virginia.
Eric DavisDepartment of Internal Medicine, University of Virginia, Charlottesville, Virginia.
Mark BeenhakkerDepartment of Pharmacology, University of Virginia, Charlottesville, Virginia.
Jaideep KapurDepartment of Neurology, University of Virginia, Charlottesville, Virginia.
Zhiyi ZuoDepartment of Anesthesiology, University of Virginia, Charlottesville, Virginia.
Nadia LunardiDepartment of Anesthesiology, University of Virginia, Charlottesville, Virginia.ORCID 0000-0002-4433-2934
University of Virginia · USMax Planck Institute of Psychiatry · DE

Funding

Secondarily generalized tonic clonic seizure; a functional anatomyR37NS119012 · NINDS · UNIVERSITY OF VIRGINIA · PI Jaideep Kapur · 2021 to 2026
$3.4M
Motor cortex plasticity in temporal lobe epilepsyR01NS120945 · NINDS · UNIVERSITY OF VIRGINIA · PI KAPUR, JAIDEEP · 2021 to 2025
$2.5M
NINDS NIH HHS R01 NS120945NINDS NIH HHS R37 NS119012
6 · The paper itself

Abstract

backgroundPrevious research suggests that sevoflurane anesthesia may prevent the brain from accessing rapid eye movement (REM) sleep. If true, then patterns of neural activity observed in REM-on and REM-off neuronal populations during recovery from sevoflurane should resemble those seen after REM sleep deprivation. In this study, the authors hypothesized that, relative to controls, animals exposed to sevoflurane present with a distinct expression pattern of c-Fos, a marker of neuronal activation, in a cluster of nuclei classically associated with REM sleep, and that such expression in sevoflurane-exposed and REM sleep-deprived animals is largely similar.

methodsAdult rats and Targeted Recombination in Active Populations mice were implanted with electroencephalographic electrodes for sleep-wake recording and randomized to sevoflurane, REM deprivation, or control conditions. Conventional c-Fos immunohistochemistry and genetically tagged c-Fos labeling were used to quantify activated neurons in a group of REM-associated nuclei in the midbrain and basal forebrain.

resultsREM sleep duration increased during recovery from sevoflurane anesthesia relative to controls (157.0 ± 24.8 min vs. 124.2 ± 27.8 min; P = 0.003) and temporally correlated with increased c-Fos expression in the sublaterodorsal nucleus, a region active during REM sleep (176.0 ± 36.6 cells vs. 58.8 ± 8.7; P = 0.014), and decreased c-Fos expression in the ventrolateral periaqueductal gray, a region that is inactive during REM sleep (34.8 ± 5.3 cells vs. 136.2 ± 19.6; P = 0.001). Fos changes similar to those seen in sevoflurane-exposed mice were observed in REM-deprived animals relative to controls (sublaterodorsal nucleus: 85.0 ± 15.5 cells vs. 23.0 ± 1.2, P = 0.004; ventrolateral periaqueductal gray: 652.8 ± 71.7 cells vs. 889.3 ± 66.8, P = 0.042).

conclusionsIn rodents recovering from sevoflurane, REM-on and REM-off neuronal activity maps closely resemble those of REM sleep-deprived animals. These findings provide new evidence in support of the idea that sevoflurane does not substitute for endogenous REM sleep. EDITOR’S PERSPECTIVE:

Indexed as

RodentiaSleep, REMAnimalsElectroencephalographyMiceProto-Oncogene Proteins c-fosRatsSevofluraneSleepSleep DeprivationProto-Oncogene Proteins c-fosSevoflurane

Identifiers

PMID38157434
PMCPMC10939895
OpenAlexW4390400371

What OpenQuestion holds

Textmetadata
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.