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Homeostatic regulation of sleep in the white-crowned sparrow (Zonotrichia leucophrys gambelii)
BACKGROUND: Sleep is regulated by both a circadian and a homeostatic process. The homeostatic process reflects the duration of prior wakefulness: the longer one stays awake, the longer and/or more intense is subsequent sleep. In mammals, the best marker of the homeostatic sleep drive is slow wave ac...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2008
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2424059/ https://www.ncbi.nlm.nih.gov/pubmed/18505569 http://dx.doi.org/10.1186/1471-2202-9-47 |
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author | Jones, Stephany G Vyazovskiy, Vladyslav V Cirelli, Chiara Tononi, Giulio Benca, Ruth M |
author_facet | Jones, Stephany G Vyazovskiy, Vladyslav V Cirelli, Chiara Tononi, Giulio Benca, Ruth M |
author_sort | Jones, Stephany G |
collection | PubMed |
description | BACKGROUND: Sleep is regulated by both a circadian and a homeostatic process. The homeostatic process reflects the duration of prior wakefulness: the longer one stays awake, the longer and/or more intense is subsequent sleep. In mammals, the best marker of the homeostatic sleep drive is slow wave activity (SWA), the electroencephalographic (EEG) power spectrum in the 0.5–4 Hz frequency range during non-rapid eye movement (NREM) sleep. In mammals, NREM sleep SWA is high at sleep onset, when sleep pressure is high, and decreases progressively to reach low levels in late sleep. Moreover, SWA increases further with sleep deprivation, when sleep also becomes less fragmented (the duration of sleep episodes increases, and the number of brief awakenings decreases). Although avian and mammalian sleep share several features, the evidence of a clear homeostatic response to sleep loss has been conflicting in the few avian species studied so far. The aim of the current study was therefore to ascertain whether established markers of sleep homeostasis in mammals are also present in the white-crowned sparrow (Zonotrichia leucophrys gambelii), a migratory songbird of the order Passeriformes. To accomplish this goal, we investigated amount of sleep, sleep time course, and measures of sleep intensity in 6 birds during baseline sleep and during recovery sleep following 6 hours of sleep deprivation. RESULTS: Continuous (24 hours) EEG and video recordings were used to measure baseline sleep and recovery sleep following short-term sleep deprivation. Sleep stages were scored visually based on 4-sec epochs. EEG power spectra (0.5–25 Hz) were calculated on consecutive 4-sec epochs. Four vigilance states were reliably distinguished based on behavior, visual inspection of the EEG, and spectral EEG analysis: Wakefulness (W), Drowsiness (D), slow wave sleep (SWS) and rapid-eye movement (REM) sleep. During baseline, SWA during D, SWS, and NREM sleep (defined as D and SWS combined) was highest at the beginning of the major sleep period and declined thereafter. Moreover, peak SWA in both SWS and NREM sleep increased significantly immediately following sleep deprivation relative to baseline. CONCLUSION: As in mammals, sleep deprivation in the white-crowned sparrow increases the intensity of sleep as measured by SWA. |
format | Text |
id | pubmed-2424059 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-24240592008-06-11 Homeostatic regulation of sleep in the white-crowned sparrow (Zonotrichia leucophrys gambelii) Jones, Stephany G Vyazovskiy, Vladyslav V Cirelli, Chiara Tononi, Giulio Benca, Ruth M BMC Neurosci Research Article BACKGROUND: Sleep is regulated by both a circadian and a homeostatic process. The homeostatic process reflects the duration of prior wakefulness: the longer one stays awake, the longer and/or more intense is subsequent sleep. In mammals, the best marker of the homeostatic sleep drive is slow wave activity (SWA), the electroencephalographic (EEG) power spectrum in the 0.5–4 Hz frequency range during non-rapid eye movement (NREM) sleep. In mammals, NREM sleep SWA is high at sleep onset, when sleep pressure is high, and decreases progressively to reach low levels in late sleep. Moreover, SWA increases further with sleep deprivation, when sleep also becomes less fragmented (the duration of sleep episodes increases, and the number of brief awakenings decreases). Although avian and mammalian sleep share several features, the evidence of a clear homeostatic response to sleep loss has been conflicting in the few avian species studied so far. The aim of the current study was therefore to ascertain whether established markers of sleep homeostasis in mammals are also present in the white-crowned sparrow (Zonotrichia leucophrys gambelii), a migratory songbird of the order Passeriformes. To accomplish this goal, we investigated amount of sleep, sleep time course, and measures of sleep intensity in 6 birds during baseline sleep and during recovery sleep following 6 hours of sleep deprivation. RESULTS: Continuous (24 hours) EEG and video recordings were used to measure baseline sleep and recovery sleep following short-term sleep deprivation. Sleep stages were scored visually based on 4-sec epochs. EEG power spectra (0.5–25 Hz) were calculated on consecutive 4-sec epochs. Four vigilance states were reliably distinguished based on behavior, visual inspection of the EEG, and spectral EEG analysis: Wakefulness (W), Drowsiness (D), slow wave sleep (SWS) and rapid-eye movement (REM) sleep. During baseline, SWA during D, SWS, and NREM sleep (defined as D and SWS combined) was highest at the beginning of the major sleep period and declined thereafter. Moreover, peak SWA in both SWS and NREM sleep increased significantly immediately following sleep deprivation relative to baseline. CONCLUSION: As in mammals, sleep deprivation in the white-crowned sparrow increases the intensity of sleep as measured by SWA. BioMed Central 2008-05-27 /pmc/articles/PMC2424059/ /pubmed/18505569 http://dx.doi.org/10.1186/1471-2202-9-47 Text en Copyright © 2008 Jones et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Jones, Stephany G Vyazovskiy, Vladyslav V Cirelli, Chiara Tononi, Giulio Benca, Ruth M Homeostatic regulation of sleep in the white-crowned sparrow (Zonotrichia leucophrys gambelii) |
title | Homeostatic regulation of sleep in the white-crowned sparrow (Zonotrichia leucophrys gambelii) |
title_full | Homeostatic regulation of sleep in the white-crowned sparrow (Zonotrichia leucophrys gambelii) |
title_fullStr | Homeostatic regulation of sleep in the white-crowned sparrow (Zonotrichia leucophrys gambelii) |
title_full_unstemmed | Homeostatic regulation of sleep in the white-crowned sparrow (Zonotrichia leucophrys gambelii) |
title_short | Homeostatic regulation of sleep in the white-crowned sparrow (Zonotrichia leucophrys gambelii) |
title_sort | homeostatic regulation of sleep in the white-crowned sparrow (zonotrichia leucophrys gambelii) |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2424059/ https://www.ncbi.nlm.nih.gov/pubmed/18505569 http://dx.doi.org/10.1186/1471-2202-9-47 |
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