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dc.contributor.authorGompf, Heinrich S.
dc.contributor.authorAnaclet, Christelle
dc.date2022-08-11T08:08:25.000
dc.date.accessioned2022-08-23T15:54:30Z
dc.date.available2022-08-23T15:54:30Z
dc.date.issued2020-06-01
dc.date.submitted2020-09-11
dc.identifier.citation<p>Gompf HS, Anaclet C. The neuroanatomy and neurochemistry of sleep-wake control. Curr Opin Physiol. 2020 Jun;15:143-151. doi: 10.1016/j.cophys.2019.12.012. Epub 2019 Dec 31. PMID: 32647777; PMCID: PMC7347132. <a href="https://doi.org/10.1016/j.cophys.2019.12.012">Link to article on publisher's site</a></p>
dc.identifier.issn2468-8673 (Linking)
dc.identifier.doi10.1016/j.cophys.2019.12.012
dc.identifier.pmid32647777
dc.identifier.urihttp://hdl.handle.net/20.500.14038/29567
dc.description.abstractSleep-wake control is dependent upon multiple brain areas widely distributed throughout the neural axis. Historically, the monoaminergic and cholinergic neurons of the ascending arousal system were the first to be discovered, and it was only relatively recently that GABAergic and glutamatergic wake- and sleep-promoting populations have been identified. Contemporary advances in molecular-genetic tools have revealed both the complexity and heterogeneity of GABAergic NREM sleep-promoting neurons as well as REM sleep-regulating populations in the brainstem such as glutamatergic neurons in the sublaterodorsal nucleus. The sleep-wake cycle progresses from periods of wakefulness to non-rapid eye movement (NREM) sleep and subsequently rapid eye movement (REM) sleep. Each vigilance stage is controlled by multiple neuronal populations, via a complex regulation that is still incompletely understood. In recent years the field has seen a proliferation in the identification and characterization of new neuronal populations involved in sleep-wake control thanks to newer, more powerful molecular genetic tools that are able to reveal neurophysiological functions via selective activation, inhibition and lesion of neuroanatomically defined sub-types of neurons that are widespread in the brain, such as GABAergic and glutamatergic neurons.
dc.language.isoen_US
dc.relation<p><a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=32647777&dopt=Abstract">Link to Article in PubMed</a></p>
dc.relation.urlhttps://doi.org/10.1016/j.cophys.2019.12.012
dc.subjectbasal forebrain
dc.subjectdorsal raphe
dc.subjectlateral hypothalamus
dc.subjectlaterodorsal and pedunculopontine tegmental nuclei
dc.subjectlocus coeruleus
dc.subjectnucleus accumbens
dc.subjectparabrachial nucleus
dc.subjectparafacial zone
dc.subjectrostromedial tegmental nucleus
dc.subjectsleep-wake circuitry
dc.subjectsublaterodorsal nucleus
dc.subjecttuberomamillary nucleus
dc.subjectventral medulla
dc.subjectventral tegmental area
dc.subjectventrolateral periaqueductal gray
dc.subjectventrolateral preoptic area
dc.subjectzona incerta
dc.subjectCellular and Molecular Physiology
dc.subjectNeuroscience and Neurobiology
dc.titleThe neuroanatomy and neurochemistry of sleep-wake control
dc.typeJournal Article
dc.source.journaltitleCurrent opinion in physiology
dc.source.volume15
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/faculty_pubs/1788
dc.identifier.contextkey19345862
html.description.abstract<p>Sleep-wake control is dependent upon multiple brain areas widely distributed throughout the neural axis. Historically, the monoaminergic and cholinergic neurons of the ascending arousal system were the first to be discovered, and it was only relatively recently that GABAergic and glutamatergic wake- and sleep-promoting populations have been identified. Contemporary advances in molecular-genetic tools have revealed both the complexity and heterogeneity of GABAergic NREM sleep-promoting neurons as well as REM sleep-regulating populations in the brainstem such as glutamatergic neurons in the sublaterodorsal nucleus. The sleep-wake cycle progresses from periods of wakefulness to non-rapid eye movement (NREM) sleep and subsequently rapid eye movement (REM) sleep. Each vigilance stage is controlled by multiple neuronal populations, via a complex regulation that is still incompletely understood. In recent years the field has seen a proliferation in the identification and characterization of new neuronal populations involved in sleep-wake control thanks to newer, more powerful molecular genetic tools that are able to reveal neurophysiological functions via selective activation, inhibition and lesion of neuroanatomically defined sub-types of neurons that are widespread in the brain, such as GABAergic and glutamatergic neurons.</p>
dc.identifier.submissionpathfaculty_pubs/1788
dc.contributor.departmentAnaclet Lab
dc.contributor.departmentNeurobiology
dc.source.pages143-151


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