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Cortical mechanisms and functional role of slow sleep oscillations

Cortical mechanisms and functional role of slow sleep oscillations
慢睡眠振荡的皮质机制和功能作用
批准号:
7936901
负责人:
MAKSIM V BAZHENOV
金额:
$31.31万
依托单位国家:
美国
项目类别:
财政年份:
2008
资助国家:
美国
项目状态:
已结题
起止时间:
2008-09-15 至 2012-08-31

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中文摘要
翻译
描述(申请人提供):这项研究的目标是了解丘脑皮质系统中慢波睡眠振荡的内在和电路机制。睡眠对健康和幸福至关重要。睡眠障碍越来越多地由生活方式和环境因素造成,可能与各种精神障碍有关。最近的研究报道,慢波睡眠对记忆的形成和巩固可能是必不可少的。揭示调节这种节律的未知机制将有助于我们理解大脑节律在正常功能和病理上的起源。在慢波睡眠(SWS)期间,整个大脑皮层网络在静默和活跃状态之间交替,每种状态持续0.2-1秒。慢振荡的超极化(无声)阶段与障碍有关,即所有皮质和丘脑神经元突触活动的一过性缺失。SWS期间的去极化(活跃)皮质状态与大脑的觉醒状态有许多相似之处。我们认为,SWS睡眠振荡是一个非常大的神经元群体的特性,它是由静默状态下微小的兴奋性突触后电位的总和引起的,它使皮质锥体细胞膜去极化到足以产生棘波,从而启动活跃的网络状态。在激活状态期间积累的固有和突触属性的变化触发向静默状态的转变。活跃状态和静默状态之间的重复转换触发了长期的突触可塑性,增强了先前清醒状态导致的突触异质性。这可能解释了SWS振荡在巩固清醒时获得的记忆痕迹中的作用。在我们的研究中,我们将使用电生理和神经解剖学技术以及不同复杂程度的计算机模拟。实验将在自然睡眠和麻醉的动物体内进行,并在体外进行脑片实验。将根据解剖学和生理学数据开发详细的Hodgkin-Huxley类型的计算机模型,并将用于研究参与SWS活动产生的特定细胞和网络机制。一个计算高效和解剖逼真的网络模型将被开发出来,该模型包含数十万个与真实突触相互连接的神经元,以模拟SWS期间丘脑皮质系统的大规模动力学。实验数据将在拉瓦尔大学使用多部位脑电和多单元记录(最多通道)、细胞内记录(最多同时记录4个神经元)及其组合来收集。实验数据的计算分析、模型开发和模拟将在索尔克研究所进行。这项研究将为进一步研究SWS在突触可塑性和记忆巩固中的作用提供基础。根据世界卫生组织的数据,流行病学数据表明,大约30%到35%的普通人口抱怨与睡眠有关的问题。睡眠障碍--尤其是睡眠呼吸暂停、睡眠不足和嗜睡--影响着7000万美国人,导致每年160亿美元的医疗费用和500亿美元的生产力损失。更好地了解睡眠过程中大脑活动的机制和功能是未来临床研究和干预的重要基础。
英文摘要
DESCRIPTION (provided by applicant): The goal of this research is to understand intrinsic and circuit mechanisms underlying slow wave sleep oscillations in the thalamocortical system. Sleep is essential for health and well-being. Sleep disturbances, increasingly caused by lifestyle and environmental factors, can be linked to a variety of mental disorders. Recent studies have reported that slow wave sleep (SWS) may be essential for memory formation and consolidation. Revealing yet unknown mechanisms mediating this rhythm will aid our understanding of the origins of brain rhythms in both normal function and pathology. During slow wave sleep (SWS) the entire cortical network alternates between silent and active states, each lasting 0.2-1 sec. The hyperpolarizing (silent) phase of the slow oscillation is associated with disfacilitation, a temporal absence of synaptic activity in all cortical and thalamic neurons. Depolarized (active) cortical states during SWS have many similarities with the wake state of the brain. We propose that SWS sleep oscillations are property of a very large neuronal population and are caused by the summation of miniature excitatory postsynaptic potentials during the silent state that depolarizes the cortical pyramidal cell membrane sufficiently for spike generation thus initiating the active network state. Changes of intrinsic and synaptic properties accumulated during the active state trigger a transition to the silent state. Repetitive transitions between active and silent states trigger long-term synaptic plasticity enhancing the synaptic heterogeneity that results from previous states of wakefulness. This may explain the role of SWS oscillations in consolidation of memory traces acquired during wakefulness. In our study we will use electrophysiological and neuroanatomical techniques and computer simulations with different levels of complexity. Experiments will be conducted on naturally sleeping and anesthetized animals in vivo and on brain slices in vitro. Detailed Hodgkin-Huxley type computer models will be developed based on anatomical and physiological data and will be used to study specific cellular and network mechanisms involved in the generation of SWS activity. A computationally efficient and anatomically realistic network models containing hundreds of thousands of neurons interconnected with realistic synapses will be developed to model large- scale dynamics of the thalamocortical system during SWS. Experimental data will be collected at Laval University using multisite EEG and multiunit recordings (up to 64 channels), intracellular recordings (up to 4 simultaneously recorded neurons), and their combination. Computational analysis of the experimental data, model development and simulations will be conducted at the Salk Institute. This study will provide a ground for future studies of the role of SWS in synaptic plasticity and memory consolidation. According to the World Health Organization (www.WHO.int), epidemiological data suggests that about 30 to 35% of the general population complains about sleep-related problems. Sleep disorders - notably sleep apnea, sleep deprivation and sleepiness - affect 70 million Americans, resulting in $16 billion in annual healthcare expenses and $50 billion in lost productivity. A better mechanistic and functional understanding of brain activity during sleep represents an important basis for future clinical research and intervention.
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