Hermanstyne Tracey O, Subedi Kalpana, Le Wei Wei, Hoffman Gloria E, Meredith Andrea L, Mong Jessica A, Misonou Hiroaki
Department of Neural and Pain Sciences ; Program in Neurosciences ; Department of Developmental Biology, Washington University, St. Louis, MO.
Sleep. 2013 Dec 1;36(12):1839-48. doi: 10.5665/sleep.3212.
The basal forebrain (BF) has been implicated as an important brain region that regulates the sleep-wake cycle of animals. Gamma-aminobutyric acidergic (GABAergic) neurons are the most predominant neuronal population within this region. However, due to the lack of specific molecular tools, the roles of the BF GABAergic neurons have not been fully elucidated. Previously, we have found high expression levels of the Kv2.2 voltage-gated potassium channel on approximately 60% of GABAergic neurons in the magnocellular preoptic area and horizontal limb of the diagonal band of Broca of the BF and therefore proposed it as a potential molecular target to study this neuronal population. In this study, we sought to determine the functional roles of the Kv2.2-expressing neurons in the regulation of the sleep-wake cycle.
Sleep analysis between two genotypes and within each genotype before and after sleep deprivation.
Animal sleep research laboratory.
Adult mice. Wild-type and Kv2.2 knockout mice with C57/BL6 background.
EEG/EMG recordings from the basal state and after sleep-deprivation which was induced by mild agitation for 6 h.
Immunostaining of a marker of neuronal activity indicates that these Kv2.2-expressing neurons appear to be preferentially active during the wake state. Therefore, we tested whether Kv2.2-expressing neurons in the BF are involved in arousal using Kv2.2-deficient mice. BF GABAergic neurons exhibited augmented expression of c-Fos. These knockout mice exhibited longer consolidated wake bouts than wild-type littermates, and that phenotype was further exacerbated by sleep deprivation. Moreover, in-depth analyses of their cortical electroencephalogram revealed a significant decrease in the delta-frequency activity during the nonrapid eye movement sleep state.
These results revealed the significance of Kv2.2-expressing neurons in the regulation of the sleep-wake cycle.
基底前脑(BF)被认为是调节动物睡眠-觉醒周期的重要脑区。γ-氨基丁酸能(GABA能)神经元是该区域最主要的神经元群体。然而,由于缺乏特异性分子工具,BF区GABA能神经元的作用尚未完全阐明。此前,我们发现Kv2.2电压门控钾通道在BF区视前大细胞区和布罗卡斜带水平支约60%的GABA能神经元上高表达,因此提出将其作为研究该神经元群体的潜在分子靶点。在本研究中,我们试图确定表达Kv2.2的神经元在调节睡眠-觉醒周期中的功能作用。
两种基因型之间以及每种基因型在睡眠剥夺前后的睡眠分析。
动物睡眠研究实验室。
成年小鼠。具有C57/BL6背景的野生型和Kv2.2基因敲除小鼠。
在基础状态和由轻度 agitation诱导6小时睡眠剥夺后进行脑电图/肌电图记录。
神经元活动标志物的免疫染色表明,这些表达Kv2.2的神经元在觉醒状态下似乎优先活跃。因此,我们使用Kv2.2缺陷小鼠测试了BF区表达Kv2.2的神经元是否参与觉醒。BF区GABA能神经元表现出c-Fos表达增加。这些基因敲除小鼠比野生型同窝小鼠表现出更长的巩固觉醒时段,并且睡眠剥夺进一步加剧了该表型。此外,对其皮质脑电图的深入分析显示,在非快速眼动睡眠状态下,δ频率活动显著降低。
这些结果揭示了表达Kv2.2的神经元在调节睡眠-觉醒周期中的重要性。