New neurons in the adult brain: the role of sleep and consequences of sleep loss
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Research over the last few decades has firmly established that new neurons are generated in selected areas of the adult mammalian brain, particularly the dentate gyrus of the hippocampal formation and the subventricular zone of the lateral ventricles. The function of adult-born neurons is still a matter of debate. In the case of the hippocampus, integration of new cells in to the existing neuronal circuitry may be involved in memory processes and the regulation of emotionality. In recent years, various studies have examined how the production of new cells and their development into neurons is affected by sleep and sleep loss. While disruption of sleep for a period shorter than one day appears to have little effect on the basal rate of cell proliferation, prolonged restriction or disruption of sleep may have cumulative effects leading to a major decrease in hippocampal cell proliferation, cell survival and neurogenesis. Importantly, while short sleep deprivation may not affect the basal rate of cell proliferation, one study in rats shows that even mild sleep restriction may interfere with the increase in neurogenesis that normally occurs with hippocampus-dependent learning. Since sleep deprivation also disturbs memory formation, these data suggest that promoting survival, maturation and integration of new cells may be an unexplored mechanism by which sleep supports learning and memory processes. Most methods of sleep deprivation that have been employed affect both non-rapid eye movement (NREM) and rapid eye movement (REM) sleep. Available data favor the hypothesis that decreases in cell proliferation are related to a reduction in REM sleep, whereas decreases in the number of cells that subsequently develop into adult neurons may be related to reductions in both NREM and REM sleep. The mechanisms by which sleep loss affects different aspects of adult neurogenesis are unknown. It has been proposed that adverse effects of sleep disruption may be mediated by stress and glucocorticoids. However, a number of studies clearly show that prolonged sleep loss can inhibit hippocampal neurogenesis independent of adrenal stress hormones. In conclusion, while modest sleep restriction may interfere with the enhancement of neurogenesis associated with learning processes, prolonged sleep disruption may even affect the basal rates of cell proliferation and neurogenesis. These effects of sleep loss may endanger hippocampal integrity, thereby leading to cognitive dysfunction and contributing to the development of mood disorders.
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Sleep dysfunction (including deprivation and fragmentation) is associated with changes in hippocampal morphology and neurogenesis in animal models.
“Experimental studies using animal models have shown that sleep dysfunction (including deprivation and fragmentation) is associated with changes in hippocampal morphology and neurogenesis.”
From Towards an Integrative Account of Potential Mechanisms Mediating the Path From Sleep Dysfunction to Hallucinations (2025) · cites this paper as [71]
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RetractedDose-Response Matters! - A Perspective on the Exercise Prescription in Exercise-Cognition Research
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- Authors
- Meerlo, P., Mistlberger, R. E., Jacobs, B. L., Craig Heller, H., & McGinty, D.
- Affiliations
- University of Groningen (NL)
- Simon Fraser University (CA)
- Princeton University (US)
- University of California, Los Angeles (US)
- Venue
- Sleep Medicine Reviews
- Publisher
- Elsevier BV
- Published
- 2009-06
- Volume
- 13
- Issue
- 3
- Pages
- 187-194
- ISSN
- 1087-0792 (ISSN-L)
- PMC
- PMC2771197
- OpenAlex
- W1968745677
- Cited by
- 318
- References
- 85
- Citations by year
- 2026: 7 · 2025: 16 · 2024: 5 · 2023: 17 · 2022: 21 · 2021: 15 · 2020: 10 · 2019: 31 · 2018: 13 · 2017: 21 · 2016: 16 · 2015: 19 · 2014: 28 · 2013: 28 · 2012: 13
- FWCI
- 1.37
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Sleep Medicine Reviews (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- University of Groningen research database (University of Groningen / Centre for Information Technology) (submittedVersion)
- Funders
- Nederlandse Organisatie voor Wetenschappelijk Onderzoek (864.04.002)
- National Institute of Mental Health (R01MH075076)
- Topics
- Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
- Life Sciences › Neuroscience › Cognitive Neuroscience › Sleep and Wakefulness Research
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Keywords
- adult neurogenesis, sleep deprivation, sleep restriction, hippocampus, dentate gyrus, subventricular zone, cell proliferation, REM sleep, NREM sleep, memory formation, hippocampus-dependent learning, glucocorticoids, stress, mood disorders, cognitive impairment
- MeSH terms
- Adult, Circadian Rhythm, Cognition Disorders, Depression, Hippocampus, Humans, Learning, Memory Disorders, Neurons, Sleep Deprivation, Sleep Stages, Stress, Psychological, Cytokines, Dentate Gyrus, Mood Disorders, Cell Proliferation, Neurogenesis
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
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