Cited by 47Sleep and Wakefulness ResearchTraumatic Brain Injury ResearchTraumatic Brain Injury and Neurovascular Disturbances

Impact of traumatic brain injury on sleep structure, electrocorticographic activity and transcriptome in mice

Sabir, Meriem, Gaudreault, Pierre-Olivier, Freyburger, Marlène, Massart, Renaud, Blanchet-Cohen, Alexis, Jaber, Manar, Gosselin, Nadia, Mongrain, Valérie·2015·Brain, Behavior, and Immunity

Abstract

Traumatic brain injury (TBI), including mild TBI (mTBI), is importantly associated with vigilance and sleep complaints. Because sleep is required for learning, plasticity and recovery, we here evaluated the bidirectional relationship between mTBI and sleep with two specific objectives: (1) Test that mTBI rapidly impairs sleep-wake architecture and the dynamics of the electrophysiological marker of sleep homeostasis (i.e., non-rapid eye movement sleep delta (1-4Hz) activity); (2) evaluate the impact of sleep loss following mTBI on the expression of plasticity markers that have been linked to sleep homeostasis and on genome-wide gene expression. A closed-head injury model was used to perform a 48h electrocorticographic (ECoG) recording in mice submitted to mTBI or Sham surgery. mTBI was found to immediately decrease the capacity to sustain long bouts of wakefulness as well as the amplitude of the time course of ECoG delta activity during wakefulness. Significant changes in ECoG spectral activity during wakefulness, non-rapid eye movement and rapid eye movement sleep were observed mainly on the second recorded day. A second experiment was performed to measure gene expression in the cerebral cortex and hippocampus after a mTBI followed either by two consecutive days of 6h sleep deprivation (SD) or of undisturbed behavior (quantitative PCR and next-generation sequencing). mTBI modified the expression of genes involved in immunity, inflammation and glial function (e.g., chemokines,…

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Crossref · 10.1016/j.bbi.2014.12.023

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  • Some animal studies report a disordered sleep phenotype of increased wakefulness, more latency to sleep, or insomnia, which are also phenotypes of sleep disorders in human TBI patients.

    “Some studies report a disordered sleep phenotype of increased wakefulness, more latency to sleep, or insomnia in animals,65,70–72 which are also phenotypes of sleep disorders in human TBI patients.”

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Authors
Sabir, M., Gaudreault, P.-O., Freyburger, M., Massart, R., Blanchet-Cohen, A., Jaber, M., Gosselin, N., & Mongrain, V.
Affiliations
  • Hôpital du Sacré-Cœur de Montréal (CA)
  • McGill University (CA)
  • Montreal Clinical Research Institute (CA)
Corresponding author
Mongrain, Valérie
Venue
Brain, Behavior, and Immunity
Publisher
Elsevier BV
Published
2015-07
Volume
47
Pages
118-130
ISSN
0889-1591 (ISSN-L)
OpenAlex
W2091321139
Cited by
47
References
7
Citations by year
2026: 2 · 2025: 6 · 2024: 3 · 2023: 6 · 2022: 5 · 2021: 1 · 2020: 3 · 2019: 8 · 2018: 3 · 2017: 2 · 2016: 6 · 2015: 2
FWCI
2.60
Type
journal article
Language
en
Open access
closed
Locations
  • Brain Behavior and Immunity (publishedVersion)
  • PubMed (publishedVersion)
Funders
  • Canadian Institutes of Health Research (CBI-127051)
  • Research Center of the Hôpital du Sacré-Coeur de Montréal
Topics
  • Life Sciences › Neuroscience › Cognitive Neuroscience › Sleep and Wakefulness Research
  • Health Sciences › Medicine › Epidemiology › Traumatic Brain Injury Research
  • Health Sciences › Medicine › Neurology › Traumatic Brain Injury and Neurovascular Disturbances
Keywords
mild traumatic brain injury, sleep-wake architecture, sleep homeostasis, electrocorticography, sleep deprivation, glial fibrillary acidic protein, Arc, neuroinflammation, glial activation, circadian rhythm, brain recovery
MeSH terms
Electrocorticography, Animals, Brain, Brain Injuries, Circadian Rhythm, Male, Sleep, Sleep Deprivation, Mice, Transcriptome

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