Härtner Lorenz, Keil Tobias W M, Kreuzer Matthias, Fritz Eva Maria, Wenning Gregor K, Stefanova Nadia, Fenzl Thomas
Department of Pharmacology and Toxicology, Institute for Pharmacy, Leopold-Franzens University of Innsbruck Innsbruck, Austria.
Neuroanesthesia Laboratory, Atlanta Veterans Affairs Medical Center/Emory University and Department of Anesthesiology, Emory University Atlanta, Georgia.
Front Behav Neurosci. 2017 Jan 10;10:252. doi: 10.3389/fnbeh.2016.00252. eCollection 2016.
Multiple system atrophy (MSA) is a neurodegenerative movement disorder characterized by parkinsonian symptoms and cerebellar symptoms. Sleep disturbances also play a crucial role in MSA. One of the most convincing animal models in MSA research is the PLP α-SYN model, but to date no studies on sleep disturbances in this mouse model, frequently found in MSA patients are available. We identified spectral shifts within the EEG of the model, strikingly resembling results of clinical studies. We also characterized muscle activity during REM sleep, which is one of the key symptoms in REM sleep behavioral disorder. Spectral shifts and REM sleep-linked muscle activity were age dependent, supporting Face Validity of the PLP α-SYN model. We also strongly suggest our findings to be critically evaluated for Predictive Validity in future studies. Currently, research on MSA lacks potential compounds attenuating or curing MSA. Future drugs must prove its potential in animal models, for this our study provides potential biomarkers.
多系统萎缩(MSA)是一种神经退行性运动障碍,其特征为帕金森症状和小脑症状。睡眠障碍在MSA中也起着关键作用。MSA研究中最具说服力的动物模型之一是PLP α - SYN模型,但迄今为止,尚未有关于该小鼠模型睡眠障碍的研究,而这种睡眠障碍在MSA患者中很常见。我们在该模型的脑电图中识别出频谱变化,这与临床研究结果惊人地相似。我们还对快速眼动睡眠期间的肌肉活动进行了特征描述,快速眼动睡眠行为障碍是快速眼动睡眠的关键症状之一。频谱变化和与快速眼动睡眠相关的肌肉活动与年龄有关,这支持了PLP α - SYN模型的表面效度。我们还强烈建议在未来的研究中对我们的发现进行批判性评估以验证其预测效度。目前,MSA研究缺乏能减轻或治愈MSA的潜在化合物。未来的药物必须在动物模型中证明其潜力,为此我们的研究提供了潜在的生物标志物。