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A subclass of evening cells promotes the switch from arousal to sleep at dusk.
Brown, Matthew P; Verma, Shubha; Palmer, Isabelle; Guerrero Zuniga, Adler; Mehta, Anuradha; Rosensweig, Clark; Keles, Mehmet F; Wu, Mark N.
Afiliación
  • Brown MP; Solomon H. Snyder Department of Neuroscience, Johns Hopkins University, Baltimore, MD 21205, USA.
  • Verma S; Department of Neurology, Johns Hopkins University, Baltimore, MD 21205, USA.
  • Palmer I; Department of Neurology, Johns Hopkins University, Baltimore, MD 21205, USA.
  • Guerrero Zuniga A; Department of Neurology, Johns Hopkins University, Baltimore, MD 21205, USA.
  • Mehta A; Department of Neurology, Johns Hopkins University, Baltimore, MD 21205, USA.
  • Rosensweig C; Department of Neurobiology, Northwestern University, Evanston, IL 60201, USA.
  • Keles MF; Department of Neurology, Johns Hopkins University, Baltimore, MD 21205, USA.
  • Wu MN; Solomon H. Snyder Department of Neuroscience, Johns Hopkins University, Baltimore, MD 21205, USA; Department of Neurology, Johns Hopkins University, Baltimore, MD 21205, USA. Electronic address: marknwu@jhmi.edu.
Curr Biol ; 34(10): 2186-2199.e3, 2024 05 20.
Article en En | MEDLINE | ID: mdl-38723636
ABSTRACT
Animals exhibit rhythmic patterns of behavior that are shaped by an internal circadian clock and the external environment. Although light intensity varies across the day, there are particularly robust differences at twilight (dawn/dusk). These periods are also associated with major changes in behavioral states, such as the transition from arousal to sleep. However, the neural mechanisms by which time and environmental conditions promote these behavioral transitions are poorly defined. Here, we show that the E1 subclass of Drosophila evening clock neurons promotes the transition from arousal to sleep at dusk. We first demonstrate that the cell-autonomous clocks of E2 neurons primarily drive and adjust the phase of evening anticipation, the canonical behavior associated with "evening" clock neurons. We next show that conditionally silencing E1 neurons causes a significant delay in sleep onset after dusk. However, rather than simply promoting sleep, activating E1 neurons produces time- and light-dependent effects on behavior. Activation of E1 neurons has no effect early in the day but then triggers arousal before dusk and induces sleep after dusk. Strikingly, these activation-induced phenotypes depend on the presence of light during the day. Despite their influence on behavior around dusk, in vivo voltage imaging of E1 neurons reveals that their spiking rate and pattern do not significantly change throughout the day. Moreover, E1-specific clock ablation has no effect on arousal or sleep. Thus, we suggest that, rather than specifying "evening" time, E1 neurons act, in concert with other rhythmic neurons, to promote behavioral transitions at dusk.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Nivel de Alerta / Sueño / Ritmo Circadiano / Drosophila melanogaster / Relojes Circadianos / Neuronas Límite: Animals Idioma: En Revista: Curr Biol Asunto de la revista: BIOLOGIA Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Nivel de Alerta / Sueño / Ritmo Circadiano / Drosophila melanogaster / Relojes Circadianos / Neuronas Límite: Animals Idioma: En Revista: Curr Biol Asunto de la revista: BIOLOGIA Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos
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