Median Preoptic Nucleus and the Control of Sleep

正中视前核和睡眠的控制

• 批准号: 8063082
• 负责人: Ronald Szymusiak
• 金额: $ 26.08万
• 依托单位: SEPULVEDA RESEARCH CORPORATION
• 依托单位国家: 美国
• 财政年份: 2002
• 资助国家: 美国
• 起止时间: 2002-03-01 至 2013-04-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8063082
• 关键词: Animals; Anxiety Disorders; Arousal; Automobile Driving; Brain Stem; Brain region; Cells; Disease; Electroencephalography; Exhibits; FOS Protein; FOS gene; Funding; Gene Expression; Glutamate Decarboxylase; Goals; Homeostasis; Hour; Imagery; Individual; Injection of therapeutic agent; Maintenance; Measures; Mental Depression; Mental disorders; Neuroanatomy; Neurons; Pattern; Post-Traumatic Stress Disorders; Posterior Hypothalamus; Preoptic Areas; Process; Progress Reports; Prosencephalon; Protocols documentation; REM Sleep; REM Sleep Deprivations; Rattus; Recovery; Research; Sleep; Sleep Deprivation; Sleep disturbances; System; Time; Tracer; Work; brain tissue; cell type; deprivation; design; nervous system disorder; neural circuit; neurochemistry; neurophysiology; preoptic nucleus; programs; response; sleep onset; sleep regulation

DESCRIPTION (provided by applicant): The regulation of sleep has a homeostatic component, as evidenced by reliable and robust increases in sleep amount and sleep depth that are a consequence of sleep deprivation. While progress has been made in identifying neurochemical and gene expression changes that accompany sleep loss, identification of neuronal circuits most crucial to homeostatic aspects of sleep regulation is lacking. In the previous funding period, we examined sleep-regulatory functions of neurons in the median preoptic nuclues (MnPN) and ventrolateral preoptic area (VLPO). We demonstrated that, similar to VLPO, the MnPN contains significant numbers of neurons that are activated during both nonREM and REM sleep compared to waking, that MnPN and VLPO sleep-active neurons are GABAergic, and that the MnPN projects to several brain regions implicated in the control of arousal, nonREM sleep and REM sleep. We also demonstrated that MnPN neurons are maximally activated during sleep deprivation and that VLPO neurons are maximally activated during recovery sleep following sleep deprivation. Activation of preoptic area neurons occurs in response to total sleep deprivation as well as in response to selective REM sleep deprivation. These latter findings identify MnPN and VLPO neurons as possible components of neural circuits regulating nonREM and REM sleep homeostasis. Proposed work will answer the following critical questions: 1) Do individual MnPN and VLPO neurons become progressively activated in association with accumulating sleep need during sleep deprivation, and de-activated as that need dissipates during recovery sleep? 2) Are adenosinergic mechanisms responsible for changes in the activity of MnPN and VLPO neurons that occur during sleep deprivation and recovery sleep? 3) Do MnPN and VLPO neurons activated during total sleep deprivation and those activated during selective REM sleep deprivation project to different brain regions? Impaired ability to initiate and maintain sleep is a prominent feature in several psychiatric disorders including, depression, post-traumatic stress disorder and anxiety disorders. Dysregulation of both nonREM and REM sleep control are seen in these diseases. Proposed work will attempt to characterize the functional neuroanatomy and the neurochemical modulation of forebrain and brainstem neural circuits that underlie normal and disordered homeostatic sleep regulation.

描述(申请人提供)：睡眠调节有一个动态平衡的组成部分，睡眠剥夺的结果是睡眠时间和睡眠深度的可靠和强劲的增加证明了这一点。虽然在识别伴随睡眠丧失的神经化学和基因表达变化方面取得了进展，但对睡眠调节的动态平衡方面最关键的神经元回路的识别还缺乏。在之前的资助期间，我们研究了正中视前核团(MnPN)和腹外侧视前区(VLPO)神经元的睡眠调节功能。我们证明，与VLPO类似，与清醒相比，MnPN在非REM和REM睡眠中都包含大量被激活的神经元，MnPN和VLPO睡眠活跃的神经元是GABA能的，并且MnPN投射到与觉醒、非REM睡眠和REM睡眠的控制有关的几个脑区。我们还证明，在睡眠剥夺期间，MnPN神经元被最大限度地激活，而VLPO神经元在睡眠剥夺后恢复睡眠期间被最大限度地激活。视前区神经元的激活是对完全睡眠剥夺和选择性快速眼动睡眠剥夺的反应。这些发现表明，MnPN和VLPO神经元可能是调节非REM和REM睡眠稳态的神经回路的组成部分。拟议的工作将回答以下关键问题：1)单个MnPN和VLPO神经元是否在睡眠剥夺期间随着睡眠需求的积累而逐渐激活，并随着睡眠需求的减少而逐渐失活？2)腺苷能机制是否与睡眠剥夺和恢复睡眠期间MnPN和VLPO神经元活动的变化有关？3)在完全睡眠剥夺和选择性REM睡眠剥夺期间激活的MnPN和VLPO神经元是否会投射到不同的脑区？启动和维持睡眠的能力受损是包括抑郁症、创伤后应激障碍和焦虑症在内的几种精神障碍的显著特征。在这些疾病中可以看到非快速眼动和快速眼动睡眠控制的失调。拟议的工作将试图描述功能神经解剖学和前脑和脑干神经回路的神经化学调节，这些回路是正常和紊乱的稳态睡眠调节的基础。

项目成果

A1 receptor mediated adenosinergic regulation of perifornical-lateral hypothalamic area neurons in freely behaving rats.

• DOI: 10.1016/j.neuroscience.2010.01.044
• 发表时间: 2010-04-28
• 期刊: Neuroscience
• 影响因子: 3.3
• 作者: Rai S;Kumar S;Alam MA;Szymusiak R;McGinty D;Alam MN
• 通讯作者: Alam MN

Functional correlates of activity in neurons projecting from the lamina terminalis to the ventrolateral periaqueductal gray.

从终板投射到腹外侧导水管周围灰质的神经元活动的功能相关性。

• DOI: 10.1111/j.1460-9568.2009.07024.x
• 发表时间: 2009
• 期刊: The European journal of neuroscience
• 作者: Uschakov,Aaron;McGinty,Dennis;Szymusiak,Ronald;McKinley,MichaelJ
• 通讯作者: McKinley,MichaelJ

GABAergic regulation of the perifornical-lateral hypothalamic neurons during non-rapid eye movement sleep in rats.

• DOI: 10.1016/j.neuroscience.2010.02.038
• 发表时间: 2010-05-19
• 期刊: NEUROSCIENCE
• 影响因子: 3.3
• 作者: Alam, M. N.;Kumar, S.;Suntsova, N.;Bashir, T.;Szymusiak, R.;McGinty, D.
• 通讯作者: McGinty, D.

Mechanisms mediating effects of nitric oxide on perifornical lateral hypothalamic neurons.

一氧化氮对穹窿外侧下丘脑神经元影响的介导机制。

• DOI: 10.1016/j.neuroscience.2012.06.014
• 发表时间: 2012
• 期刊: Neuroscience
• 影响因子: 3.3
• 作者: Kostin,A;McGinty,D;Szymusiak,R;Alam,MN
• 通讯作者: Alam,MN

Maturation of sleep homeostasis in developing rats: a role for preoptic area neurons.

发育中大鼠睡眠稳态的成熟：视前区神经元的作用。

• DOI: 10.1152/ajpregu.00727.2010
• 发表时间: 2011
• 期刊: American journal of physiology. Regulatory, integrative and comparative physiology
• 作者: Gvilia,Irma;Suntsova,Natalia;Angara,Bryan;McGinty,Dennis;Szymusiak,Ronald
• 通讯作者: Szymusiak,Ronald