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年龄和性别对儿童发作性睡病小鼠模型的影响。

The Impacts of Age and Sex in a Mouse Model of Childhood Narcolepsy.

作者信息

Coffey Alissa A, Joyal Adam A, Yamanaka Akihiro, Scammell Thomas E

机构信息

Department of Neurology, Beth Israel Deaconess Medical Center and Harvard Medical School, Boston, MA, United States.

Department of Neuroscience II, Research Institute of Environmental Medicine, Nagoya University, Nagoya, Japan.

出版信息

Front Neurosci. 2021 Mar 4;15:644757. doi: 10.3389/fnins.2021.644757. eCollection 2021.

Abstract

Narcolepsy is a sleep disorder caused by selective death of the orexin neurons that often begins in childhood. Orexin neuron loss disinhibits REM sleep during the active period and produces cataplexy, episodes of paralysis during wakefulness. Cataplexy is often worse when narcolepsy develops in children compared to adults, but the reason for this difference remains unknown. We used mice to model narcolepsy at different ages. When doxycycline is removed from the diet, the orexin neurons of these mice express diphtheria toxin A and die within 2-3 weeks. We removed doxycycline at 4 weeks (young-onset) or 14 weeks (adult-onset) of age in male and female mice. We implanted electroencephalography (EEG) and electromyography (EMG) electrodes for sleep recordings two weeks later and then recorded EEG/EMG/video for 24 h at 3 and 13 weeks after removal of doxycycline. Age-matched controls had access to doxycycline diet for the entire experiment. Three weeks after doxycycline removal, both young-onset and adult-onset mice developed severe cataplexy and the sleep-wake fragmentation characteristic of narcolepsy. Cataplexy and maintenance of wake were no worse in young-onset compared to adult-onset mice, but female mice had more bouts of cataplexy than males. Orexin neuron loss was similarly rapid in both young- and adult-onset mice. As age of orexin neuron loss does not impact the severity of narcolepsy symptoms in mice, the worse symptoms in children with narcolepsy may be due to more rapid orexin neuron loss than in adults.

摘要

发作性睡病是一种由食欲素神经元选择性死亡引起的睡眠障碍,通常始于儿童期。食欲素神经元的丧失会在清醒期解除对快速眼动睡眠的抑制,并导致猝倒,即清醒时的麻痹发作。与成年人相比,儿童患发作性睡病时猝倒往往更严重,但这种差异的原因尚不清楚。我们使用小鼠对不同年龄段的发作性睡病进行建模。当从饮食中去除强力霉素时,这些小鼠的食欲素神经元会表达白喉毒素A,并在2至3周内死亡。我们在雄性和雌性小鼠4周龄(幼年发病)或14周龄(成年发病)时去除强力霉素。两周后,我们植入脑电图(EEG)和肌电图(EMG)电极进行睡眠记录,然后在去除强力霉素后的3周和13周记录24小时的EEG/EMG/视频。年龄匹配的对照组在整个实验过程中可以食用含强力霉素的饮食。去除强力霉素三周后,幼年发病和成年发病的小鼠都出现了严重的猝倒以及发作性睡病特有的睡眠-觉醒碎片化。与成年发病的小鼠相比,幼年发病的小鼠在猝倒和维持清醒方面并无更严重的情况,但雌性小鼠的猝倒发作比雄性小鼠更多。幼年发病和成年发病的小鼠中食欲素神经元的丧失速度相似。由于食欲素神经元丧失的年龄并不影响小鼠发作性睡病症状的严重程度,发作性睡病儿童症状更严重可能是因为其食欲素神经元丧失比成年人更快。

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