<oai_dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
  <dc:creator>Mang, Géraldine M.</dc:creator>
  <dc:creator>La Spada, Francesco</dc:creator>
  <dc:creator>Emmenegger, Yann</dc:creator>
  <dc:creator>Chappuis, Sylvie</dc:creator>
  <dc:creator>Ripperger, Jürgen A.</dc:creator>
  <dc:creator>Albrecht, Urs</dc:creator>
  <dc:creator>Franken, Paul</dc:creator>
  <dc:date>2016-03-01</dc:date>
  <dc:description xmlns:ns0="xml" ns0:lang="en">Study Objectives: The nuclear receptor REV-ERBα is a potent, constitutive  transcriptional repressor critical for the regulation of key circadian and metabolic  genes. Recently, REV-ERBα's involvement in learning, neurogenesis, mood, and  dopamine turnover was demonstrated suggesting a specific role in central nervous  system functioning. We have previously shown that the brain expression of several  core clock genes, including Rev-erbα, is modulated by sleep loss. We here test the  consequences of a loss of REV-ERBα on the homeostatic regulation of sleep.Methods:  EEG/EMG signals were recorded in Rev-erbα knockout (KO) mice and their wild type  (WT) littermates during baseline, sleep deprivation, and recovery. Cortical gene  expression measurements after sleep deprivation were contrasted to baseline.Results:  Although baseline sleep/wake duration was remarkably similar, KO mice showed an  advance of the sleep/wake distribution relative to the light-dark cycle. After sleep onset  in baseline and after sleep deprivation, both EEG delta power (1–4 Hz) and sleep  consolidation were reduced in KO mice indicating a slower increase of homeostatic  sleep need during wakefulness. This slower increase might relate to the smaller  increase in theta and gamma power observed in the waking EEG prior to sleep onset  under both conditions. Indeed, the increased theta activity during wakefulness  predicted delta power in subsequent NREM sleep. Lack of Rev-erbα increased Bmal1,  Npas2, Clock, and Fabp7 expression, confirming the direct regulation of these genes  by REV-ERBα also in the brain.Conclusions: Our results add further proof to the notion  that clock genes are involved in sleep homeostasis. Because accumulating evidence  directly links REV-ERBα to dopamine signaling the altered homeostatic regulation of  sleep reported here are discussed in that context.</dc:description>
  <dc:format>application/pdf</dc:format>
  <dc:identifier>https://folia.unifr.ch/global/documents/304922</dc:identifier>
  <dc:identifier>https://folia.unifr.ch/documents/304922/files/alb_ash.pdf</dc:identifier>
  <dc:language>eng</dc:language>
  <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.5665/sleep.5534</dc:relation>
  <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
  <dc:rights>License undefined</dc:rights>
  <dc:source>SLEEP. - 2016, vol. 39, no. 3, p. 589–601</dc:source>
  <dc:subject>info:eu-repo/classification/udc/57</dc:subject>
  <dc:title xmlns:ns1="xml" ns1:lang="en">Altered sleep homeostasis in rev-erbα knockout mice</dc:title>
  <dc:type>http://purl.org/coar/resource_type/c_6501</dc:type>
</oai_dc:dc>
