Presynaptic Release Probability Determines the Need for Sleep

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Abstract

Sleep is universal among animals with synapses, yet the synaptic functions determining the need for sleep remain elusive. By directly measuring synaptic transmission at anatomically defined synapses in Drosophila , we found that synaptic strength remained stable or declined after sleep deprivation in a circuit-specific manner. In contrast, presynaptic release probability (P r ) consistently decreased with sleep loss across circuits and species, stemming from reduced Ca 2+ influx or weakened vesicle–channel coupling at presynaptic terminals, and recovered after sleep. Bidirectional manipulations of P r altered sleep pressure, establishing a causal relationship between presynaptic function and sleep need. Non-synaptic sleep-regulatory signaling pathways consistently modulate P r but not synaptic strength. Thus, our findings identify P r , rather than synaptic strength, as the conserved synaptic substrate underlying sleep need.

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