Cited by 57Sleep and Wakefulness ResearchCircadian rhythm and melatoninNerve injury and regeneration

Short-term sleep disturbance enhances brain-derived neurotrophic factor gene expression in rat hippocampus by acting as internal stressor

Fujihara, Hiroaki, Sei, Hiroyoshi, Morita, Yusuke, Ueta, Yoichi, Morita, Kyoji·2003·Journal of Molecular Neuroscience

Abstract

Rats were subjected to nonselective sleep disturbance for short periods under conditions designed to minimize the adverse influence of external stresses, such as environmental conditions and restricted movement, and both brain-derived neurotrophic factor (BDNF) protein and its mRNA levels in the brain were then determined to investigate the influence of sleep disturbance itself on BDNF gene expression. Total sleep duration was partially but significantly reduced by disturbing the sleep/wake cycle for 1 and 2 h, gradually increased according to the time of disturbance, then returned to control levels at 6 h after the beginning of sleep disturbance. Under these conditions, the slight but significant elevation of corticotrophin-releasing factor (CRF) mRNA levels in the paraventricular nucleus (PVN) was observed at an early stage of the sleep disturbance period. Sleep disturbance induced the elevation of both BDNF protein and its mRNA levels in the hippocampus but not in the cerebellum or the brainstem, and the elevated BDNF mRNA expression in the hippocampus returned toward basal levels during the sleep recovery period when the rebound of sleep duration was observed. These findings suggest the possibility that short-term disturbance of the sleep/wake cycle and, hence, the partial reduction of non-REM sleep duration, might exert a potential influence on neuronal and/or glial cells as an internal stressor, resulting in the elevation of BDNF gene expression in rat hippocampus.

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Crossref · 10.1385/jmn:21:3:223

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  • The mechanisms by which sleep loss activates ACTH release are likely to involve increased brain CRH levels rather than increased pituitary sensitivity to CRH.

    “The mechanisms by which sleep loss activates ACTH release are likely to involve increased brain CRH levels rather than increased pituitary sensitivity to CRH, because rodents studies have reported enhanced brain synthesis and release of CRH (32–34) but also reduced CRH binding in the pituitary (32) after acute and chronic sleep restriction.”

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References 45 · Cited by 57

Authors
Fujihara, H., Sei, H., Morita, Y., Ueta, Y., & Morita, K.
Affiliations
  • Tokushima University (JP)
  • University of Occupational and Environmental Health Japan (JP)
Corresponding author
Morita, Kyoji
Venue
Journal of Molecular Neuroscience
Published
2003
Volume
21
Issue
3
Pages
223-232
ISSN
0895-8696 (ISSN-L)
OpenAlex
W2034442556
Cited by
57
References
45
Citations by year
2025: 4 · 2024: 6 · 2023: 1 · 2022: 1 · 2021: 3 · 2020: 1 · 2019: 3 · 2018: 2 · 2017: 4 · 2016: 4 · 2015: 4 · 2014: 7 · 2013: 3
FWCI
0.84
Type
journal article
Language
en
Open access
closed
Locations
  • Journal of Molecular Neuroscience (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Life Sciences › Neuroscience › Cognitive Neuroscience › Sleep and Wakefulness Research
  • Life Sciences › Neuroscience › Endocrine and Autonomic Systems › Circadian rhythm and melatonin
  • Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Nerve injury and regeneration
Keywords
sleep disorders, brain-derived neurotrophic factor, BDNF expression, hippocampus, corticotropin-releasing factor, paraventricular nucleus, sleep-wake cycle, NREM sleep, sleep recovery
MeSH terms
Animals, Corticotropin-Releasing Hormone, Hippocampus, Hypothalamo-Hypophyseal System, Male, Paraventricular Hypothalamic Nucleus, RNA, Messenger, Sleep Deprivation, Sleep, REM, Stress, Physiological, Up-Regulation, Rats, Wistar, Brain-Derived Neurotrophic Factor, Rats

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