Local sleep homeostasis in the avian brain: convergence of sleep function in mammals and birds?
Open accessAbstract
The function of the brain activity that defines slow wave sleep (SWS) and rapid eye movement (REM) sleep in mammals is unknown. During SWS, the level of electroencephalogram slow wave activity (SWA or 0.5-4.5 Hz power density) increases and decreases as a function of prior time spent awake and asleep, respectively. Such dynamics occur in response to waking brain use, as SWA increases locally in brain regions used more extensively during prior wakefulness. Thus, SWA is thought to reflect homeostatically regulated processes potentially tied to maintaining optimal brain functioning. Interestingly, birds also engage in SWS and REM sleep, a similarity that arose via convergent evolution, as sleeping reptiles and amphibians do not show similar brain activity. Although birds deprived of sleep show global increases in SWA during subsequent sleep, it is unclear whether avian sleep is likewise regulated locally. Here, we provide, to our knowledge, the first electrophysiological evidence for local sleep homeostasis in the avian brain. After staying awake watching David Attenborough's The Life of Birds with only one eye, SWA and the slope of slow waves (a purported marker of synaptic strength) increased only in the hyperpallium--a primary visual processing region--neurologically connected to the stimulated eye. Asymmetries were specific to the hyperpallium, as the non-visual mesopallium showed a symmetric increase in SWA and wave slope. Thus, hypotheses for the function of mammalian SWS…
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In birds, sensory deprivation of one eye while watching a documentary about birds increased SWA and the slope of slow waves only in the hyperpallium connected to the stimulated eye.
“In birds, sensory deprivation of one eye while watching a documentary about birds increased SWA and the slope of slow waves only in the hyperpallium (a primary visual region) connected to the stimulated eye (726).”
From About Sleep's Role in Memory (2013) · cites this paper as [726]
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References 80 · Cited by 112
- Authors
- Lesku, J. A., Vyssotski, A. L., Martinez-Gonzalez, D., Wilzeck, C., & Rattenborg, N. C.
- Affiliations
- Max Planck Institute for Ornithology (DE)
- University of Zurich (CH)
- Sleep and Flight Group, Max Planck Institute for Ornithology, Seewiesen, Germany
- Goethe University Frankfurt (DE)
- Corresponding author
- Rattenborg, Niels C.
- Venue
- Proceedings of the Royal Society B: Biological Sciences
- Publisher
- The Royal Society
- Published
- 2011-01-05
- Volume
- 278
- Issue
- 1717
- Pages
- 2419-2428
- ISSN
- 0080-4649 (ISSN-L)
- 0962-8452
- 1471-2954
- PMC
- PMC3125620
- OpenAlex
- W2125132127
- Cited by
- 112
- References
- 80
- Citations by year
- 2026: 2 · 2025: 7 · 2024: 6 · 2023: 6 · 2022: 3 · 2021: 7 · 2020: 12 · 2019: 15 · 2018: 7 · 2017: 9 · 2016: 10 · 2015: 5 · 2014: 7 · 2013: 5 · 2012: 8
- FWCI
- 3.73
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Proceedings of the Royal Society B Biological Sciences (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- MPG.PuRe (Max Planck Society) (submittedVersion)
- Zurich Open Repository and Archive (University of Zurich) (submittedVersion)
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Sleep and Wakefulness Research
- Life Sciences › Neuroscience › Cognitive Neuroscience › Neural dynamics and brain function
- Social Sciences › Psychology › Experimental and Cognitive Psychology › Sleep and related disorders
- Keywords
- sleep homeostasis, slow-wave sleep, REM sleep, avian brain, slow-wave activity, mesopallium, visual stimulation, synaptic efficacy, convergent evolution, sleep deprivation, EEG
- MeSH terms
- Animals, Brain, Electrodes, Implanted, Electroencephalography, Female, Fourier Analysis, Homeostasis, Male, Columbidae, Signal Processing, Computer-Assisted, Sleep, Sleep Deprivation, Wakefulness
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