<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Tisdale RK</submitter><funding>NHLBI NIH HHS</funding><funding>National Institutes of Health</funding><funding>NIH HHS</funding><pagination>e14037</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10950840</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>33(3)</volume><pubmed_abstract>Aversive symptoms, including insomnia experienced during opioid withdrawal, are a major drive to relapse; however, withdrawal-associated sleep symptomatology has been little explored in preclinical models. We describe here a model of opioid withdrawal in mice that resembles the sleep phenotype characteristic of withdrawal in humans. Male and female C57BL/6 mice were instrumented with telemeters to record electroencephalogram, electromyogram, activity and subcutaneous temperature. All mice received two treatments separated by a 16-day washout period: (1) saline (volume: 10 ml kg&lt;sup>-1&lt;/sup>); or (2) ascending doses of morphine (5, 10, 20, 40 and 80 mg kg&lt;sup>-1&lt;/sup>; volume: 10 ml kg&lt;sup>-1&lt;/sup>) for 5 days at Zeitgeber time 1 and Zeitgeber time 13. Recordings for the first 71 hr after treatment discontinuation (withdrawal days 1-3) and for 24 hr on withdrawal days 5 and 7 were scored for sleep/wake state, and sleep architecture and electroencephalogram spectral data were analysed. Morphine was acutely wake- and activity-promoting, and non-rapid eye movement and rapid eye movement sleep were increased during the dark phase on withdrawal day 2 in both sexes. While non-rapid eye movement delta power (0.5-4.0 Hz), a measure of sleep intensity, was reduced during the light phase on withdrawal day 1 and the dark phase on withdrawal day 2 in both sexes, female mice also exhibited changes in the duration and the number of bouts of sleep/wake states. These observations of fragmented sleep on withdrawal days 1-3 suggest poorer sleep consolidation and a more pronounced withdrawal-associated sleep phenotype in female than in male mice. These data may indicate a greater sensitivity to morphine, a more distinct aversive sleep phenotype and/or a faster escalation to dependence in female mice.</pubmed_abstract><journal>Journal of sleep research</journal><pubmed_title>Biological sex influences sleep phenotype in mice experiencing spontaneous opioid withdrawal.</pubmed_title><pmcid>PMC10950840</pmcid><funding_grant_id>R01 HL150836</funding_grant_id><funding_grant_id>R01HL150836</funding_grant_id><pubmed_authors>Allocca G</pubmed_authors><pubmed_authors>Tisdale RK</pubmed_authors><pubmed_authors>Haire M</pubmed_authors><pubmed_authors>Ma SC</pubmed_authors><pubmed_authors>Kilduff TS</pubmed_authors><pubmed_authors>Bruchas MR</pubmed_authors><pubmed_authors>Sun Y</pubmed_authors><pubmed_authors>Park S</pubmed_authors><pubmed_authors>Morairty SR</pubmed_authors></additional><is_claimable>false</is_claimable><name>Biological sex influences sleep phenotype in mice experiencing spontaneous opioid withdrawal.</name><description>Aversive symptoms, including insomnia experienced during opioid withdrawal, are a major drive to relapse; however, withdrawal-associated sleep symptomatology has been little explored in preclinical models. We describe here a model of opioid withdrawal in mice that resembles the sleep phenotype characteristic of withdrawal in humans. Male and female C57BL/6 mice were instrumented with telemeters to record electroencephalogram, electromyogram, activity and subcutaneous temperature. All mice received two treatments separated by a 16-day washout period: (1) saline (volume: 10 ml kg&lt;sup>-1&lt;/sup>); or (2) ascending doses of morphine (5, 10, 20, 40 and 80 mg kg&lt;sup>-1&lt;/sup>; volume: 10 ml kg&lt;sup>-1&lt;/sup>) for 5 days at Zeitgeber time 1 and Zeitgeber time 13. Recordings for the first 71 hr after treatment discontinuation (withdrawal days 1-3) and for 24 hr on withdrawal days 5 and 7 were scored for sleep/wake state, and sleep architecture and electroencephalogram spectral data were analysed. Morphine was acutely wake- and activity-promoting, and non-rapid eye movement and rapid eye movement sleep were increased during the dark phase on withdrawal day 2 in both sexes. While non-rapid eye movement delta power (0.5-4.0 Hz), a measure of sleep intensity, was reduced during the light phase on withdrawal day 1 and the dark phase on withdrawal day 2 in both sexes, female mice also exhibited changes in the duration and the number of bouts of sleep/wake states. These observations of fragmented sleep on withdrawal days 1-3 suggest poorer sleep consolidation and a more pronounced withdrawal-associated sleep phenotype in female than in male mice. These data may indicate a greater sensitivity to morphine, a more distinct aversive sleep phenotype and/or a faster escalation to dependence in female mice.</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 May</publication><modification>2025-07-12T03:04:33.794Z</modification><creation>2025-07-12T03:04:33.794Z</creation></dates><accession>S-EPMC10950840</accession><cross_references><pubmed>37731248</pubmed><doi>10.1111/jsr.14037</doi></cross_references></HashMap>