Sidney Aki , Morgan Brown , Jerry Stitzel , Hunter Mathews
{"title":"尼古丁对雌性C57BL/6J小鼠睡眠的影响","authors":"Sidney Aki , Morgan Brown , Jerry Stitzel , Hunter Mathews","doi":"10.1016/j.bbr.2025.115754","DOIUrl":null,"url":null,"abstract":"<div><div>Sleep disturbances during nicotine withdrawal are well-documented and strongly linked to relapse. While previous studies, including our lab’s work in male mice (Mathews & Stitzel, 2019), have characterized the effects of nicotine exposure and abstinence on sleep, potential sex differences remain unclear. Given that biological sex influences both nicotine addiction and sleep regulation, understanding its role in withdrawal-induced sleep disturbances is critical.</div><div>This study examines the effects of nicotine exposure and abstinence on sleep in female C57BL/6 J mice using EEG/EMG recordings to assess sleep architecture and spectral power. Mice underwent chronic oral nicotine self-administration followed by abstinence, allowing for a detailed analysis of NREM and REM sleep metrics, sleep fragmentation, and EEG spectral power. Nicotine access significantly reduced total sleep time and NREM sleep while increasing sleep fragmentation and REM bout duration. During abstinence, females exhibited persistent NREM fragmentation, a hallmark of withdrawal-induced sleep disruption linked to hyperarousal and relapse vulnerability. Additionally, spectral power analyses revealed that nicotine exposure and abstinence strongly influenced EEG spectral patterns when examined by vigilance state, with the most pronounced alterations occurring during NREM and REM sleep.</div><div>Compared to males from our previous study, female mice displayed a more robust sleep fragmentation phenotype during abstinence, suggesting heightened sensitivity to withdrawal-induced sleep disturbances. These findings emphasize the importance of sex-specific mechanisms in nicotine addiction and support targeting withdrawal-related sleep disruptions to improve relapse prevention strategies for nicotine use disorder.</div></div>","PeriodicalId":8823,"journal":{"name":"Behavioural Brain Research","volume":"495 ","pages":"Article 115754"},"PeriodicalIF":2.3000,"publicationDate":"2025-08-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"The effects of nicotine on sleep in female C57BL/6J mice\",\"authors\":\"Sidney Aki , Morgan Brown , Jerry Stitzel , Hunter Mathews\",\"doi\":\"10.1016/j.bbr.2025.115754\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Sleep disturbances during nicotine withdrawal are well-documented and strongly linked to relapse. While previous studies, including our lab’s work in male mice (Mathews & Stitzel, 2019), have characterized the effects of nicotine exposure and abstinence on sleep, potential sex differences remain unclear. Given that biological sex influences both nicotine addiction and sleep regulation, understanding its role in withdrawal-induced sleep disturbances is critical.</div><div>This study examines the effects of nicotine exposure and abstinence on sleep in female C57BL/6 J mice using EEG/EMG recordings to assess sleep architecture and spectral power. Mice underwent chronic oral nicotine self-administration followed by abstinence, allowing for a detailed analysis of NREM and REM sleep metrics, sleep fragmentation, and EEG spectral power. Nicotine access significantly reduced total sleep time and NREM sleep while increasing sleep fragmentation and REM bout duration. During abstinence, females exhibited persistent NREM fragmentation, a hallmark of withdrawal-induced sleep disruption linked to hyperarousal and relapse vulnerability. Additionally, spectral power analyses revealed that nicotine exposure and abstinence strongly influenced EEG spectral patterns when examined by vigilance state, with the most pronounced alterations occurring during NREM and REM sleep.</div><div>Compared to males from our previous study, female mice displayed a more robust sleep fragmentation phenotype during abstinence, suggesting heightened sensitivity to withdrawal-induced sleep disturbances. These findings emphasize the importance of sex-specific mechanisms in nicotine addiction and support targeting withdrawal-related sleep disruptions to improve relapse prevention strategies for nicotine use disorder.</div></div>\",\"PeriodicalId\":8823,\"journal\":{\"name\":\"Behavioural Brain Research\",\"volume\":\"495 \",\"pages\":\"Article 115754\"},\"PeriodicalIF\":2.3000,\"publicationDate\":\"2025-08-04\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Behavioural Brain Research\",\"FirstCategoryId\":\"102\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0166432825003419\",\"RegionNum\":3,\"RegionCategory\":\"心理学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"BEHAVIORAL SCIENCES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Behavioural Brain Research","FirstCategoryId":"102","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0166432825003419","RegionNum":3,"RegionCategory":"心理学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"BEHAVIORAL SCIENCES","Score":null,"Total":0}
The effects of nicotine on sleep in female C57BL/6J mice
Sleep disturbances during nicotine withdrawal are well-documented and strongly linked to relapse. While previous studies, including our lab’s work in male mice (Mathews & Stitzel, 2019), have characterized the effects of nicotine exposure and abstinence on sleep, potential sex differences remain unclear. Given that biological sex influences both nicotine addiction and sleep regulation, understanding its role in withdrawal-induced sleep disturbances is critical.
This study examines the effects of nicotine exposure and abstinence on sleep in female C57BL/6 J mice using EEG/EMG recordings to assess sleep architecture and spectral power. Mice underwent chronic oral nicotine self-administration followed by abstinence, allowing for a detailed analysis of NREM and REM sleep metrics, sleep fragmentation, and EEG spectral power. Nicotine access significantly reduced total sleep time and NREM sleep while increasing sleep fragmentation and REM bout duration. During abstinence, females exhibited persistent NREM fragmentation, a hallmark of withdrawal-induced sleep disruption linked to hyperarousal and relapse vulnerability. Additionally, spectral power analyses revealed that nicotine exposure and abstinence strongly influenced EEG spectral patterns when examined by vigilance state, with the most pronounced alterations occurring during NREM and REM sleep.
Compared to males from our previous study, female mice displayed a more robust sleep fragmentation phenotype during abstinence, suggesting heightened sensitivity to withdrawal-induced sleep disturbances. These findings emphasize the importance of sex-specific mechanisms in nicotine addiction and support targeting withdrawal-related sleep disruptions to improve relapse prevention strategies for nicotine use disorder.
期刊介绍:
Behavioural Brain Research is an international, interdisciplinary journal dedicated to the publication of articles in the field of behavioural neuroscience, broadly defined. Contributions from the entire range of disciplines that comprise the neurosciences, behavioural sciences or cognitive sciences are appropriate, as long as the goal is to delineate the neural mechanisms underlying behaviour. Thus, studies may range from neurophysiological, neuroanatomical, neurochemical or neuropharmacological analysis of brain-behaviour relations, including the use of molecular genetic or behavioural genetic approaches, to studies that involve the use of brain imaging techniques, to neuroethological studies. Reports of original research, of major methodological advances, or of novel conceptual approaches are all encouraged. The journal will also consider critical reviews on selected topics.