Bryan R. Alava, Andrew R. Morris, Andrew C. Liu, Jose F. Abisambra, Karyn A. Esser
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引用次数: 0
摘要
tau蛋白病患者的睡眠时间和数量障碍持续存在。利用传统脑电图(EEG)和最近的压电睡眠小鼠行为跟踪系统(PiezoSleep Mouse Behavioral Tracking System)在原发性tau神经病理的转基因模型中对此进行了研究。在这里,我们利用 8 号血清型腺相关病毒(AAV8),通过脑室内注射人类突变体 hSyn-P301L-tau,建立了原发性 tau 病模型。我们利用无创压电睡眠系统(PiezoSleep System)发现,在表达 AAV8-P301L tau 的雌雄小鼠中,睡眠结构的数量和时间都发生了改变。AAV8-P301L tau小鼠的睡眠持续时间与年龄相关,特别是在活跃期开始时显著增加,这表明与tauopathy相关的睡眠障碍发生在一天中的一个关键而敏感的时间段。由于我们的研究结果表明睡眠行为在一天中特定的过渡时期会发生变化,因此tau神经病变可能会影响生物过程的正常昼夜变化,这一点应使用AAV8-P301L tau病模型进行探索。
AAV8-P301L tau expression confers age-related disruptions in sleep quantity and timing
Sleep timing and quantity disturbances persist in tauopathy patients. This has been studied in transgenic models of primary tau neuropathology using traditional electroencephalograms (EEGs) and more recently, the PiezoSleep Mouse Behavioral Tracking System. Here, we generated a primary tauopathy model using an intracerebroventricular injection of human mutant hSyn-P301L-tau, using adeno-associated virus of serotype 8 (AAV8). We discovered distinctions in sleep architecture with altered quantity and timing in AAV8-P301L tau expressing mice of both sexes using the noninvasive PiezoSleep System. The AAV8-P301L tau mice exhibit striking age-related increases in sleep duration specifically at the active phase onset, suggesting a critical and sensitive time-of-day for tauopathy related sleep disturbances to occur. Since our findings show sleep behavior changes at specific transitional periods of the day, tau neuropathology may impact normal diurnal variation in biological processes, which should be explored using the AAV8-P301L tauopathy model.