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A Mechanism for Learning with Sleep Spindles

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Specialty Biology
Date 2020 Apr 7
PMID 32248788
Citations 34
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Abstract

Spindles are ubiquitous oscillations during non-rapid eye movement (NREM) sleep. A growing body of evidence points to a possible link with learning and memory, and the underlying mechanisms are now starting to be unveiled. Specifically, spindles are associated with increased dendritic activity and high intracellular calcium levels, a situation favourable to plasticity, as well as with control of spiking output by feed-forward inhibition. During spindles, thalamocortical networks become unresponsive to inputs, thus potentially preventing interference between memory-related internal information processing and extrinsic signals. At the system level, spindles are co-modulated with other major NREM oscillations, including hippocampal sharp wave-ripples (SWRs) and neocortical slow waves, both previously shown to be associated with learning and memory. The sequential occurrence of reactivation at the time of SWRs followed by neuronal plasticity-promoting spindles is a possible mechanism to explain NREM sleep-dependent consolidation of memories. This article is part of the Theo Murphy meeting issue 'Memory reactivation: replaying events past, present and future'.

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References
1.
Gambino F, Pages S, Kehayas V, Baptista D, Tatti R, Carleton A . Sensory-evoked LTP driven by dendritic plateau potentials in vivo. Nature. 2014; 515(7525):116-9. DOI: 10.1038/nature13664. View

2.
Buzsaki G . Hippocampal sharp wave-ripple: A cognitive biomarker for episodic memory and planning. Hippocampus. 2015; 25(10):1073-188. PMC: 4648295. DOI: 10.1002/hipo.22488. View

3.
Ulrich D . Sleep Spindles as Facilitators of Memory Formation and Learning. Neural Plast. 2016; 2016:1796715. PMC: 4826925. DOI: 10.1155/2016/1796715. View

4.
Fernandez L, Luthi A . Sleep Spindles: Mechanisms and Functions. Physiol Rev. 2019; 100(2):805-868. DOI: 10.1152/physrev.00042.2018. View

5.
Stickgold R, Walker M . Sleep-dependent memory triage: evolving generalization through selective processing. Nat Neurosci. 2013; 16(2):139-45. PMC: 5826623. DOI: 10.1038/nn.3303. View