Evidence map›Paper›PMID 38288298›Full record

ArticleNeurotrauma reports2024

Lifelong Chronic Sleep Disruption in a Mouse Model of Traumatic Brain Injury.

Andrew R Morris, Erwin K Gudenschwager Basso, Miguel A Gutierrez-Monreal, Rawad Daniel Arja, Firas H Kobeissy, Christopher G Janus, Kevin K W Wang, Jiepei Zhu, Andrew C Liu

Open access · goldAbstract read
In one paragraph

Article in Neurotrauma reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
1.7field-weighted citation impact, top 18% 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

1 citing paper in PubMed, 5 citations in OpenAlex.

  1. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 2 institutions in 1 country.

Andrew R MorrisDepartment of Physiology and Aging, Department of Neuroscience, University of Florida College of Medicine, Gainesville, Florida, USA.
Erwin K Gudenschwager BassoDepartment of Physiology and Aging, Department of Neuroscience, University of Florida College of Medicine, Gainesville, Florida, USA.
Miguel A Gutierrez-MonrealDepartment of Physiology and Aging, Department of Neuroscience, University of Florida College of Medicine, Gainesville, Florida, USA.
Rawad Daniel ArjaCenter for Neurotrauma, Multiomics & Biomarkers, Department of Neurobiology and Neuroscience Institute, Morehouse School of Medicine, Atlanta, Georgia, USA.
Firas H KobeissyCenter for Neurotrauma, Multiomics & Biomarkers, Department of Neurobiology and Neuroscience Institute, Morehouse School of Medicine, Atlanta, Georgia, USA.
Christopher G JanusCenter for Translational Research in Neurodegenerative Disease (CTRND), Department of Neuroscience, University of Florida College of Medicine, Gainesville, Florida, USA.
Kevin K W WangCenter for Neurotrauma, Multiomics & Biomarkers, Department of Neurobiology and Neuroscience Institute, Morehouse School of Medicine, Atlanta, Georgia, USA.
Jiepei ZhuCenter for Neurotrauma, Multiomics & Biomarkers, Department of Neurobiology and Neuroscience Institute, Morehouse School of Medicine, Atlanta, Georgia, USA.
Andrew C LiuDepartment of Physiology and Aging, Department of Neuroscience, University of Florida College of Medicine, Gainesville, Florida, USA.
University of Florida · USMorehouse School of Medicine · US

Funding

Deregulation of Sleep/Wake Homeostasis by Binge Alcohol Use Following Traumatic Brain InjuryR21AA029785 · NIAAA · UNIVERSITY OF FLORIDA · PI LIU, ANDREW C. · 2022 to 2023
$388k
NIAAA NIH HHS R21 AA029785
6 · The paper itself

Abstract

Chronic sleep/wake disturbances (SWDs) are strongly associated with traumatic brain injury (TBI) in patients and are being increasingly recognized. However, the underlying mechanisms are largely understudied and there is an urgent need for animal models of lifelong SWDs. The objective of this study was to develop a chronic TBI rodent model and investigate the lifelong chronic effect of TBI on sleep/wake behavior. We performed repetitive midline fluid percussion injury (rmFPI) in 4-month-old mice and monitored their sleep/wake behavior using the non-invasive PiezoSleep system. Sleep/wake states were recorded before injury (baseline) and then monthly thereafter. We found that TBI mice displayed a significant decrease in sleep duration in both the light and dark phases, beginning at 3 months post-TBI and continuing throughout the study. Consistent with the sleep phenotype, these TBI mice showed circadian locomotor activity phenotypes and exhibited reduced anxiety-like behavior. TBI mice also gained less weight, and had less lean mass and total body water content, compared to sham controls. Further, TBI mice showed extensive brain tissue loss and increased glial fibrillary acidic protein and ionized calcium-binding adaptor molecule 1 levels in the hypothalamus and vicinity of the injury, indicative of chronic neuropathology. In summary, our study identified a critical time window of TBI pathology and associated circadian and sleep/wake phenotypes. Future studies should leverage this mouse model to investigate the molecular mechanisms underlying the chronic sleep/wake phenotypes post-TBI early in life.

Indexed as

chronic brain injurycircadian rhythmmidline fluid percussion injury (mFPI)PiezoSleepsleep/wake disturbancestraumatic brain injury (TBI)

Identifiers

PMID38288298
PMCPMC10823169
OpenAlexW4391017454

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.