Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Jones, Stephany G, Vyazovskiy, Vladyslav V, Cirelli, Chiara, Tononi, Giulio, Benca, Ruth M
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2008
Materias:
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
_version_ 1782156241506664448
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
work_keys_str_mv AT jonesstephanyg homeostaticregulationofsleepinthewhitecrownedsparrowzonotrichialeucophrysgambelii
AT vyazovskiyvladyslavv homeostaticregulationofsleepinthewhitecrownedsparrowzonotrichialeucophrysgambelii
AT cirellichiara homeostaticregulationofsleepinthewhitecrownedsparrowzonotrichialeucophrysgambelii
AT tononigiulio homeostaticregulationofsleepinthewhitecrownedsparrowzonotrichialeucophrysgambelii
AT bencaruthm homeostaticregulationofsleepinthewhitecrownedsparrowzonotrichialeucophrysgambelii