We recently proposed a comprehensive framework for sleep-dependent memory consolidation suggesting that, during slow-wave sleep (SWS), memory representations are transferred from a temporary to a long-term store and thereby undergo reorganization in a process of system consolidation (The memory function of sleep. Nature Rev. Neurosci. 11, 114–126 (2010))1. Further, we suggested that this system consolidation process is complemented by the strengthening of synaptic connections — that is, synaptic consolidation — during the ensuing rapid eye movement (REM) sleep. Walker and Stickgold extend this framework by specifying cognitive features that are essential to the process of memory reorganization during sleep (Overnight alchemy: sleep-dependent memory evolution. Nature Rev. Neurosci. 19 Feb 2010 (doi:10.1038/nrn2762-c1))2. Four processes are proposed: an initial hippocampal binding of separate neocortical memory traces, followed by the unitization, assimilation and abstraction of more generalized representations at the neocortical level. This is an elegant cognitive concept that compellingly integrates some recent findings on the effects of sleep on problem-solving tasks.
However, Walker and Stickgold's proposal2 to link such processes of reorganization to REM sleep seems to be at some variance with the available experimental evidence. Forming part of a superordinate system consolidation process, the proposed 'evolutionary' stages of memory consolidation are more likely to take place during SWS, for three reasons. First, the reorganization of memory representations requires the reactivation of the representations. At the neuronal level, memory reactivation seems to occur most robustly during SWS3,4,5 and rarely during REM sleep. Of note, reports of dreams after awakenings from REM sleep in this context are often mistaken for indicators of the occurrence of memory reactivation during REM sleep. However, such reports are generated while the brain is 'awake' and do not necessarily provide an accurate picture of the processes that actually take place during REM sleep. Second, there is considerable evidence (summarized in Ref. 1) that electrophysiological phenomena linked to SWS, such as sharp wave-ripples, spindles and slow oscillations, coordinately contribute to the transfer of memory information from the hippocampus to the neocortex, a process that is thought to underlie the proposed reorganization of memory representations6,7. Low acetylcholinergic tone, which occurs during SWS, is a further prerequisite for such transfer8,9. Third, a direct comparison of the effects of REM-rich and SWS-rich sleep has provided solid behavioural evidence that the proposed process of 'abstraction' — that is, gaining insight into hidden rules — benefits from SWS rather than REM sleep10.
All this does not exclude a contribution of REM sleep to the reorganization of memories beyond that of a synaptic strengthening of the reorganized (neocortical) representations. However, the ultimate contributions of REM sleep to memory consolidation have so far remained enigmatic11. Given the many proposals for the role of REM sleep in memory, it seems that the time is ripe to subject some of these proposals to systematic scrutiny.
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Sirota, A., Csicsvari, J., Buhl, D. & Buzsaki, G. Communication between neocortex and hippocampus during sleep in rodents. Proc. Natl Acad. Sci. USA 100, 2065–2069 (2003).
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Gais, S. & Born, J. Low acetylcholine during slow-wave sleep is critical for declarative memory consolidation. Proc. Natl Acad. Sci. USA 101, 2140–2144 (2004).
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Diekelmann, S., Born, J. Slow-wave sleep takes the leading role in memory reorganization. Nat Rev Neurosci 11, 218 (2010). https://doi.org/10.1038/nrn2762-c2
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