神经素-1的缺失影响了雌性小鼠的醒/睡结构、节律性和非节律性皮质电图活动。

IF 3.3 3区 医学 Q2 NEUROSCIENCES
Cassandra C Areal, Nicolas Lemmetti, Tanya Leduc, Clément Bourguignon, Jean-Marc Lina, Erika Bélanger-Nelson, Valérie Mongrain
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引用次数: 0

摘要

神经素-1 (NLGN1)是一种与谷氨酸神经传递相关的突触粘附分子,在行为状态和认知功能的调节中起作用。研究显示,在雄性小鼠清醒和睡眠期间,它可以塑造皮质电图(ECoG)活动,包括基线条件下的非周期性活动。鉴于神经素(Nlgn)的表达在性别之间存在差异,我们在此旨在描述NLGN1缺失对雌性动物觉醒和睡眠结构、节律性和非节律性活动动力学以及睡眠剥夺反应的影响。将Nlgn1敲除(KO)雌性小鼠和野生型(WT)雌性窝鼠植入ECoG电极,记录ECoG信号48小时,包括24小时基线,然后剥夺6小时睡眠和18小时无干扰恢复(REC)。研究了清醒、慢波睡眠(SWS)和矛盾睡眠(PS)的时间及其交替,并使用标准谱分析和多重分形分析对ECoG活动进行了量化。与WT雌性相比,Nlgn1 KO雌性在基线下的光照期花在PS上的时间更长。观察这种差异随着更多PS发作和整体PS波持续时间短,表明一个支离破碎的PS。此外,Nlgn1 KO女性显示少8和13赫兹之间ECoG权力后,1.25和3.5 Hz之间少权力在PS,和更多的在2.5和3.75之间赫兹在慢波睡眠相比WT。在基线和REC, Nlgn1缺乏女性显著关联到一个更高的价值最普遍的赫斯特指数(Hm)在慢波睡眠,这表明ECoG非周期活动在各个尺度上的持久性更高。在KO女性的SWS期间,也发现了赫斯特指数在Hm周围弥散的日常动态变化的迹象。本研究强调了缺乏NLGN1的雌性小鼠在清醒/睡眠结构、周期性(节律性)和非周期性(不规则性/多重分形)活动方面的差异。这些发现为NLGN1在形成ECoG组织中的作用提供了额外的支持,特别是在睡眠期间,并将有助于理解神经精神疾病中睡眠障碍的起源。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The absence of Neuroligin-1 shapes wake/sleep architecture, rhythmic and arrhythmic activities of the electrocorticogram in female mice.

Associated to glutamatergic neurotransmission, Neuroligin-1 (NLGN1) is a synaptic adhesion molecule with roles in the regulation of behavioral states and cognitive function. It was shown to shape electrocorticographic (ECoG) activity during wakefulness and sleep in male mice, including aperiodic activity under baseline conditions. Given that the expression of Neuroligins (Nlgn) differs between sexes, we here aim to characterize the impact of the absence of NLGN1 on the wakefulness and sleep architecture, rhythmic and arrhythmic activity dynamics, and responses to sleep deprivation in female animals. Nlgn1 knockout (KO) female mice and wild-type (WT) female littermates were implanted with ECoG electrodes, and ECoG signals were recorded for 48 hours comprising a 24-hour baseline, followed by a 6-hour sleep deprivation and 18 hours of undisturbed recovery (REC). Time spent in wakefulness, slow wave sleep (SWS) and paradoxical sleep (PS), and their alternation were interrogated, and ECoG activities were quantified using a standard spectral analysis and a multifractal analysis. Nlgn1 KO females spent more time in PS during the light period under baseline in comparison to WT females. This difference was observed along with more PS bouts and a shorter overall PS bout duration, indicative of a fragmented PS. Additionally, Nlgn1 KO females displayed less ECoG power between 8 and 13 Hz during wake, less power between 1.25 and 3.5 Hz during PS, and more between 2.5 and 3.75 Hz during SWS in comparison to WT. Under both baseline and REC, NLGN1 absence in females was significantly associated with a higher value of the most prevalent Hurst exponent (Hm) during SWS, which points to a higher persistence across scales of ECoG aperiodic activity. Indications for alterations in the daily dynamics of the Dispersion of Hurst exponents around Hm were also found during SWS in KO females. The present study highlights differences in wake/sleep architecture, and in periodic (rhythmic) and aperiodic (arrhythmic/multifractal) activities in female mice lacking NLGN1. These findings provide additional support to a role for NLGN1 in shaping the ECoG organization, in particular during sleep, and will help understanding the origin of sleep disturbances in neuropsychiatric diseases.

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来源期刊
Molecular Brain
Molecular Brain NEUROSCIENCES-
CiteScore
7.30
自引率
0.00%
发文量
97
审稿时长
>12 weeks
期刊介绍: Molecular Brain is an open access, peer-reviewed journal that considers manuscripts on all aspects of studies on the nervous system at the molecular, cellular, and systems level providing a forum for scientists to communicate their findings. Molecular brain research is a rapidly expanding research field in which integrative approaches at the genetic, molecular, cellular and synaptic levels yield key information about the physiological and pathological brain. These studies involve the use of a wide range of modern techniques in molecular biology, genomics, proteomics, imaging and electrophysiology.
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