Department of Physiology, Anatomy and Genetics, University of Oxford, Parks Road, Oxford, OX1 3PT, United Kingdom; Sleep and Circadian Neuroscience Institute, Oxford Molecular Pathology Institute, Sir William Dunn School of Pathology, South Parks Road, Oxford OX1 3RE, United Kingdom.
Department of Experimental Psychology, University of Oxford,South Parks Road, Oxford OX1 3UD, United Kingdom.
Curr Opin Neurobiol. 2017 Jun;44:202-211. doi: 10.1016/j.conb.2017.05.002. Epub 2017 May 30.
The importance of sleep for behavioural performance during waking is long-established, but the underlying reasons and mechanisms remain elusive. Waking and sleep are associated with changes in the levels of GluA1 AMPAR subunit in synaptic membranes, while studies using genetically-modified mice have identified an important role for GluA1-dependent synaptic plasticity in a non-associative form of memory that underlies short-term habituation to recently experienced stimuli. Here we posit that sleep may play a role in dishabituation, which restores attentional capacity and maximises the readiness of the animal for learning and goal-directed behaviour during subsequent wakefulness. Furthermore we suggest that sleep disturbance may fundamentally change the nature of behaviour, making it more model-free and habitual as a result of reduced attentional capacity.
睡眠对于清醒时行为表现的重要性早已确立,但背后的原因和机制仍然难以捉摸。清醒和睡眠与突触膜中 GluA1 AMPAR 亚基水平的变化有关,而使用基因修饰小鼠的研究表明,GluA1 依赖性突触可塑性在一种非联想形式的记忆中起着重要作用,这种记忆是最近经历的刺激的短期习惯化的基础。在这里,我们假设睡眠可能在去习惯化中发挥作用,去习惯化恢复了注意力容量,并使动物在随后的清醒状态下为学习和目标导向行为做好最大准备。此外,我们还认为,睡眠障碍可能从根本上改变行为的本质,使其由于注意力容量降低而变得更加无模型化和习惯性。