对急性睡眠剥夺的恢复能力与海马介导的学习障碍的减弱有关。

Amanda Lee, Haoyi Lei, Lida Zhu, Zhou Jiang, Warren Ladiges
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引用次数: 0

摘要

背景:睡眠不足是一个普遍问题,对个人的影响各不相同。有些人的表现会有所欠缺,而有些人则能保持高水平的体力和脑力活动,因而具有恢复能力。众所周知,睡眠不足会导致学习和记忆等方面的认知功能障碍,但人们对有助于恢复这种不良影响的神经机制却知之甚少:方法:利用现有的睡眠不足和非睡眠不足的16至18个月大的C57BL/6小鼠学习范例数据库,根据代表每只小鼠学习曲线的R2值来识别快速学习者和缓慢学习者:结果表明,与快速学习者相比,睡眠不足的小鼠有更多的慢速学习者,而非睡眠不足的小鼠则相反。海马免疫组化和数字成像分析表明,与睡眠不足的慢速学习者相比,睡眠不足的快速学习者表达较低水平的单核细胞趋化蛋白-1和组蛋白去乙酰化酶2,而表达较高水平的突触素和脑源性神经营养因子:这些观察结果提供了证据,表明在认知试验中表现良好的睡眠不足小鼠表现出较少的海马介导的学习障碍,并为进一步研究随着年龄增长睡眠不足对神经生物学的恢复能力提供了依据。
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Resilience to acute sleep deprivation is associated with attenuation of hippocampal mediated learning impairment.

Background: Sleep deprivation is a universal issue that affects individuals in different ways. While some individuals experience a deficit in performance, others experience resiliency as they maintain high levels of physical and mental activity. Sleep loss is known to cause cognitive dysfunction in areas such as learning and memory, but little is known about neural mechanisms that contribute to resilience to this adverse effect.

Methods: An existing database of a learning paradigm in sleep deprived and non-sleep deprived 16 to 18-month old C57BL/6 mice was used to identify fast learners and slow learners based on an R2 value representing the learning curve of each individual mouse.

Results: Results showed that sleep deprived mice had more slow learners compared to fast learners whereas non-sleep-deprived mice showed the opposite. Hippocampal immunohistochemistry and digital imaging analysis showed sleep deprived, fast learners expressed lower levels of monocyte chemoattractant protein-1 and histone deacetylase 2 and higher levels of synaptophysin and brain-derived neurotrophic factor compared to sleep-deprived slow learners.

Conclusions: These observations provide evidence to suggest that sleep-deprived mice that performed well in a cognitive assay show less hippocampal mediated learning impairment and provide the rationale for further investigations into neurobiological resilience to sleep deprivation with increasing age.

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