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睡眠压力调节斑马鱼单神经元突触数量。

Sleep pressure modulates single-neuron synapse number in zebrafish.

机构信息

Department of Cell and Developmental Biology, University College London, London, UK.

UCL Ear Institute, University College London, London, UK.

出版信息

Nature. 2024 May;629(8012):639-645. doi: 10.1038/s41586-024-07367-3. Epub 2024 May 1.

Abstract

Sleep is a nearly universal behaviour with unclear functions. The synaptic homeostasis hypothesis proposes that sleep is required to renormalize the increases in synaptic number and strength that occur during wakefulness. Some studies examining either large neuronal populations or small patches of dendrites have found evidence consistent with the synaptic homeostasis hypothesis, but whether sleep merely functions as a permissive state or actively promotes synaptic downregulation at the scale of whole neurons is unclear. Here, by repeatedly imaging all excitatory synapses on single neurons across sleep-wake states of zebrafish larvae, we show that synapses are gained during periods of wake (either spontaneous or forced) and lost during sleep in a neuron-subtype-dependent manner. However, synapse loss is greatest during sleep associated with high sleep pressure after prolonged wakefulness, and lowest in the latter half of an undisrupted night. Conversely, sleep induced pharmacologically during periods of low sleep pressure is insufficient to trigger synapse loss unless adenosine levels are boosted while noradrenergic tone is inhibited. We conclude that sleep-dependent synapse loss is regulated by sleep pressure at the level of the single neuron and that not all sleep periods are equally capable of fulfilling the functions of synaptic homeostasis.

摘要

睡眠是一种几乎普遍存在的行为,其功能尚不清楚。突触稳态假说提出,睡眠是恢复清醒时突触数量和强度增加所必需的。一些研究检查了大型神经元群体或小的树突片,发现了与突触稳态假说一致的证据,但睡眠是否仅仅作为一种许可状态起作用,或者是否在整个神经元的规模上主动促进突触下调尚不清楚。在这里,我们通过在斑马鱼幼虫的睡眠-觉醒状态下反复对单个神经元上的所有兴奋性突触进行成像,表明在清醒期间(无论是自发的还是强迫的)获得突触,并以神经元亚型依赖的方式在睡眠期间丢失突触。然而,在长时间清醒后与高睡眠压力相关的睡眠期间,突触丢失最大,在未中断的夜间后半段最小。相反,在低睡眠压力期间通过药理学诱导的睡眠不足以触发突触丢失,除非在抑制去甲肾上腺素能张力的同时增加腺苷水平。我们得出结论,睡眠依赖的突触丢失是由单个神经元水平的睡眠压力调节的,并非所有睡眠阶段都同样能够满足突触稳态的功能。

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