Wakefulness and Forebrain Activation by Orexin Neurons

食欲素神经元的觉醒和前脑激活

• 批准号: 8243531
• 负责人: THOMAS E SCAMMELL
• 金额: $ 46.27万
• 依托单位: BETH ISRAEL DEACONESS MEDICAL CENTER
• 依托单位国家: 美国
• 财政年份: 2011
• 资助国家: 美国
• 起止时间: 2011-03-01 至 2015-02-28
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8243531
• 关键词: AMPA Receptors; Address; Affect; Anatomy; Animals; Arousal; Automobile Driving; Behavior; Brain region; Chronic; Clinical; Code; Disease; Drowsiness; Dynorphins; Electrophysiology (science); Exposure to; Foundations; Genetic; Glutamates; Goals; Hypercapnia; Hypothalamic structure; In Situ Hybridization; Lateral; Lead; Life; Maintenance; Maps; Medial; Mediating; Modeling; Molecular Biology; Mus; Neurobiology; Neurons; Neuropeptides; Obstructive Sleep Apnea; Pathway interactions; Patients; Peptides; Phenotype; Physiological; Play; Prefrontal Cortex; Prosencephalon; Protocols documentation; Receptor Gene; Research Personnel; Resources; Role; Signal Transduction; Site; Sleep; Sleep Apnea Syndromes; Sleep Disorders; Slice; Techniques; Testing; Thalamic structure; Time; Wakefulness; adeno-associated viral vector; basal forebrain; benefit sharing; cholinergic; cholinergic neuron; dynorphin receptor; effective therapy; experience; hypocretin; improved; insight; kappa opioid receptors; multidisciplinary; neural circuit; neurochemistry; neuromechanism; neurotransmission; novel; parabrachial nucleus; patch clamp; postsynaptic; presynaptic; prevent; programs; receptor; receptor expression; recombinase; relating to nervous system; research study; response

Arousal from obstructive sleep apnea (OSA) plays a life-saving role, and we hypothesize that it is supported by the same circuitry that produces arousal during normal wakefulness. The orexin neurons in the lateral hypothalamus play a critical role in producing arousal, and lack of orexin neurotransmission produces a chronic state of hypoarousal. These studies will provide key insights into an important aspect of this Program Project: Defining the mechanisms through which the orexin neurons ultimately activate the cortex. We present a testable model in which the orexin neurons promote arousal by exciting basal forebrain neurons that activate the cortex. In addition to the orexin peptides, the orexin neurons probably co-release the inhibitory neuropeptide dynorphin, and we hypothesize that dynorphin and orexin act synergistically in the basal forebrain to promote full arousal. We will use powerful genetic, anatomic, and physiologic techniques to identify the neural circuits through which the orexin neurons promote arousal. To define the brain regions through which orexin promotes arousal, we will study sleep/wake behavior in mice that express orexin receptors only in the basal forebrain, thalamus, or cortex. Using slice recordings, we will determine the pre- and postsynaptic effects of orexin and dynorphin on neurochemically-defined basal forebrain neurons, including those projecting to prefrontal cortex. We will also map the basal forebrain pathways through which orexin and dynorphin promote wakefulness. Collectively, these multidisciplinary experiments will define the pathways through which orexin, in combination with dynorphin, promotes cortical activation, thus providing an anatomic and physiologic framework to better understand the neurobiology of arousal and the clinical problem of sleepiness.

阻塞性睡眠呼吸暂停（OSA）引起的唤醒起着挽救生命的作用，我们假设它是由正常清醒时产生唤醒的相同回路支持的。外侧下丘脑中的食欲素神经元在产生唤醒中起关键作用，并且缺乏食欲素神经传递产生慢性低唤醒状态。这些研究将为该计划项目的一个重要方面提供关键见解：定义食欲素神经元最终激活皮层的机制。 我们提出了一个可测试的模型，其中食欲素神经元通过兴奋基底前脑促进唤醒 激活皮质的神经元。除了食欲肽，食欲肽神经元可能共同释放抑制性神经肽强啡肽，我们假设，强啡肽和食欲肽协同作用，在基底前脑，以促进充分唤醒。 我们将使用强大的遗传学、解剖学和生理学技术来识别食欲素神经元促进唤醒的神经回路。为了确定食欲素促进唤醒的大脑区域，我们将研究只在基底前脑、丘脑或皮质表达食欲素受体的小鼠的睡眠/觉醒行为。使用切片记录，我们将确定食欲素和强啡肽对神经化学定义的基底前脑神经元，包括投射到前额皮质的神经元的突触前和突触后效应。我们还将绘制基底前脑的通路，食欲素和强啡肽通过这些通路促进觉醒。 总的来说，这些多学科实验将确定食欲素， 与强啡肽结合，促进皮质激活，从而提供解剖和生理上的 框架，以更好地了解唤醒的神经生物学和嗜睡的临床问题。