The price of being awake and the function of sleep: synaptic homeostasis
Please contact Fiona Woods (fiona.woods@cncb.ox.ac.uk) to arrange individual meetings with Prof. Chiara Cirelli
Sleep is universal, tightly regulated, and many cognitive functions are impaired if we do not sleep. But why? Any hypothesis about the essential function of sleep must take into account that when asleep we are essentially offline: sensory disconnection must be crucial for whatever function sleep serves. If not, natural selection would likely have found a way to perform the same function while awake, avoiding the danger of being unable to monitor the environment.
Over the past 20 years, we have developed and tested a comprehensive hypothesis about the core function of sleep: The Synaptic Homeostasis Hypothesis (SHY). SHY states that sleep is the price we pay for brain plasticity. During wakefulness the excitatory synapses that allow neurons to communicate with each other undergo net potentiation as a result of learning, an ongoing process that happens all the time while we are awake, constantly adapting to an ever-changing environment.
The plasticity of the brain is essential for survival but is also a costly process, because stronger synapses increase the demand for energy and cellular supplies, lead to decreases in signal-to-noise ratios, and saturate the ability to learn. According to SHY, the renormalization of synaptic strength should mainly occur during sleep when the brain is disconnected from the environment and neural circuits can be broadly reactivated off-line to undergo a systematic and yet specific synaptic down-selection. This renormalization favors memory consolidation and the integration of new with old memories, and eliminates the synapses that contribute more to the “noise” than to the “signal.” Just as crucially, synaptic renormalization during sleep restores the homeostasis of energy and cellular supplies, including many proteins and lipids that are part of the synapses, with beneficial effects at both the systems and cellular level.
I will discuss the rationale underlying this hypothesis and summarize electrophysiological, molecular and ultrastructural studies in flies, rodents and humans that confirmed SHY’s main predictions, including the recent observation, obtained using serial block face scanning electron microscopy, that most synapses in mouse primary motor and sensory cortices grow after wake and shrink after sleep. I will then present unpublished ultrastructural data obtained in the hippocampus and in the cortex of mouse pups. Finally, I will examine recent studies by other groups showing the causal role of cortical slow waves and hippocampal ripples in sleep-dependent synaptic down-selection, and some of the molecular mechanisms that can mediate this process.
Date:
10 December 2018, 16:00 (Monday, 10th week, Michaelmas 2018)
Venue:
Le Gros Clark Building, off South Parks Road OX1 3QX
Venue Details:
large lecture theatre
Speaker:
Prof Chiara Cirelli (University of Wisconsin–Madison, USA)
Organisers:
Centre for Neural Circuits and Behaviour,
Cortex Club (University of Oxford)
Organiser contact email address:
cortex.club@studentclubs.ox.ac.uk
Part of:
Cortex Club - Oxford Neuroscience Society
Booking required?:
Not required
Cost:
free
Audience:
Members of the University only
Editor:
Lukas Krone
