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February 28, 2026Nature Communications1 citationsOpen Access

Disrupted temperature-sleep coupling mechanism in a Dravet syndrome mouse model

SFSaja FadilaGKGeorgii KrivosheinHMHala Majadly

Key Points

  • This research aims to understand the mechanisms behind sleep disturbances and thermal dysregulation in Dravet syndrome.
  • Used Dravet syndrome mice (Scn1a A1783V) to study sleep and thermoregulation.
  • Conducted electrocorticography and local field potential recordings.
  • Monitored core body temperature during sleep transitions.
  • Compared responses to warmth between Dravet syndrome and wild-type mice.
  • Dravet syndrome mice showed lower core body temperature compared to control mice.
  • A lack of core temperature change was observed in DS mice during sleep onset.
  • Warmth did not promote sleep in DS mice, unlike in wild-type mice.
  • Restoration of warmth-induced sleep was achieved through SCN1A expression or chemogenetic stimulation of the hypothalamus.

Abstract

Abstract Dravet syndrome (DS) is associated with epilepsy, developmental delays, thermal dysregulation, and sleep disturbances. While seizures have been linked to hippocampal dysfunction, what drives sleep disturbances and thermal dysregulation is poorly understood. Using DS mice ( Scn1a A1783V ), we identified a link between sleep and thermoregulation. We found that DS mice exhibited lower core body temperature. Next, using electrocorticography, local field potential recordings, and core temperature monitoring, we showed that DS mice exhibited a lack of core temperature change during the transition from waking to non-rapid eye movement sleep. This is in contrast to wild-type (WT) mice, in which sleep onset coincided with a temperature drop. Additionally, warmth promoted sleep in WT, but not in DS mice. Vector-mediated expression of SCN1A or chemogenetic stimulation of the anterior hypothalamus restored the warmth-induced somnogenesis in DS mice. These findings highlight a connection between sleep and thermal dysregulation in DS, implicating altered neuronal activity of the hypothalamus.

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Cite This Study

Fadila et al. (2026) studied this question.

synapsesocial.com/papers/69a286da0a974eb0d3c0210chttps://doi.org/10.1038/s41467-026-69957-1
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