{"title":"睡眠/觉醒相关功能的生物学机制。","authors":"Greene Robert","doi":"10.1016/j.biopsych.2025.06.002","DOIUrl":null,"url":null,"abstract":"<p><p>Animals oscillate between sleep and wake periods characterized by foraging for food and avoiding danger, with a relatively high level of arousal during waking, and by relative absence of movement and decreased level of arousal during sleep. In the brain, at the cellular level, waking involves energy efficient oxidative phosphorylation that can conserve metabolites, whereas during sleep, energy and metabolites are utilized to support protein anabolism and turnover. At the intercellular level this bias in metabolism can facilitate sleep-dependent glutamate synaptic reorganization by downscaling synaptic strength and enhancement of metaplastic potentiating plasticity. The dual focus of this review is on the molecules and genetics in the intracellular pathways controlling the functionally permissive state of sleep and the functional outcomes of sleep. These sleep-related functional outcomes require MEF2c-dependent transcriptional changes targeting genes regulating glutamate synapses. The same genes are enriched for known risk factor genes for autism spectrum disorder consistent with an interaction of sleep and autism.</p>","PeriodicalId":8918,"journal":{"name":"Biological Psychiatry","volume":" ","pages":""},"PeriodicalIF":9.0000,"publicationDate":"2025-06-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Biological mechanisms of sleep/wake related function.\",\"authors\":\"Greene Robert\",\"doi\":\"10.1016/j.biopsych.2025.06.002\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Animals oscillate between sleep and wake periods characterized by foraging for food and avoiding danger, with a relatively high level of arousal during waking, and by relative absence of movement and decreased level of arousal during sleep. In the brain, at the cellular level, waking involves energy efficient oxidative phosphorylation that can conserve metabolites, whereas during sleep, energy and metabolites are utilized to support protein anabolism and turnover. At the intercellular level this bias in metabolism can facilitate sleep-dependent glutamate synaptic reorganization by downscaling synaptic strength and enhancement of metaplastic potentiating plasticity. The dual focus of this review is on the molecules and genetics in the intracellular pathways controlling the functionally permissive state of sleep and the functional outcomes of sleep. These sleep-related functional outcomes require MEF2c-dependent transcriptional changes targeting genes regulating glutamate synapses. The same genes are enriched for known risk factor genes for autism spectrum disorder consistent with an interaction of sleep and autism.</p>\",\"PeriodicalId\":8918,\"journal\":{\"name\":\"Biological Psychiatry\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":9.0000,\"publicationDate\":\"2025-06-10\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Biological Psychiatry\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1016/j.biopsych.2025.06.002\",\"RegionNum\":1,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"NEUROSCIENCES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Biological Psychiatry","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1016/j.biopsych.2025.06.002","RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"NEUROSCIENCES","Score":null,"Total":0}
Biological mechanisms of sleep/wake related function.
Animals oscillate between sleep and wake periods characterized by foraging for food and avoiding danger, with a relatively high level of arousal during waking, and by relative absence of movement and decreased level of arousal during sleep. In the brain, at the cellular level, waking involves energy efficient oxidative phosphorylation that can conserve metabolites, whereas during sleep, energy and metabolites are utilized to support protein anabolism and turnover. At the intercellular level this bias in metabolism can facilitate sleep-dependent glutamate synaptic reorganization by downscaling synaptic strength and enhancement of metaplastic potentiating plasticity. The dual focus of this review is on the molecules and genetics in the intracellular pathways controlling the functionally permissive state of sleep and the functional outcomes of sleep. These sleep-related functional outcomes require MEF2c-dependent transcriptional changes targeting genes regulating glutamate synapses. The same genes are enriched for known risk factor genes for autism spectrum disorder consistent with an interaction of sleep and autism.
期刊介绍:
Biological Psychiatry is an official journal of the Society of Biological Psychiatry and was established in 1969. It is the first journal in the Biological Psychiatry family, which also includes Biological Psychiatry: Cognitive Neuroscience and Neuroimaging and Biological Psychiatry: Global Open Science. The Society's main goal is to promote excellence in scientific research and education in the fields related to the nature, causes, mechanisms, and treatments of disorders pertaining to thought, emotion, and behavior. To fulfill this mission, Biological Psychiatry publishes peer-reviewed, rapid-publication articles that present new findings from original basic, translational, and clinical mechanistic research, ultimately advancing our understanding of psychiatric disorders and their treatment. The journal also encourages the submission of reviews and commentaries on current research and topics of interest.