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      NREM sleep spindles are associated with dream recall

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          Abstract

          Both rapid eye movement (REM) sleep dreaming and non-rapid eye movement (NREM) sleep spindles have been linked to processes of memory consolidation. However, relationships between the two phenomena have yet to be explored. In a heterogeneous sample of 53 healthy subjects who had participated in a memory consolidation protocol and who varied in their self-reported recall of dreams and nightmares, we assessed overnight polysomnography, N2 sleep spindle density, REM dream word count, and retrospective estimates of how often they recall dreams, bad dreams (dysphoric dreams, no awakening), and nightmares (dysphoric dreams, with awakenings). Fast spindle density positively correlated with all measures of dream recall but was most robustly associated with bad dream recall and REM dream word count. Correlations with bad dream recall were particularly strong for spindles occurring in sleep cycles 2 and 3 and correlations with word count for cycles 1, 4, and 5. While slow spindle density showed opposite correlations with all of these measures, partialing out slow spindles attenuated, but did not eliminate, the fast spindle correlations. Results are largely consistent with the conclusion that fast sleep spindles are associated with a common trait factor that also influences dream recall. However, the results also raise the possibility that both spindles and dreaming are expressions of memory consolidation mechanisms, such as neural replay, that transcend sleep stage.

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          Most cited references88

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          About sleep's role in memory.

          Over more than a century of research has established the fact that sleep benefits the retention of memory. In this review we aim to comprehensively cover the field of "sleep and memory" research by providing a historical perspective on concepts and a discussion of more recent key findings. Whereas initial theories posed a passive role for sleep enhancing memories by protecting them from interfering stimuli, current theories highlight an active role for sleep in which memories undergo a process of system consolidation during sleep. Whereas older research concentrated on the role of rapid-eye-movement (REM) sleep, recent work has revealed the importance of slow-wave sleep (SWS) for memory consolidation and also enlightened some of the underlying electrophysiological, neurochemical, and genetic mechanisms, as well as developmental aspects in these processes. Specifically, newer findings characterize sleep as a brain state optimizing memory consolidation, in opposition to the waking brain being optimized for encoding of memories. Consolidation originates from reactivation of recently encoded neuronal memory representations, which occur during SWS and transform respective representations for integration into long-term memory. Ensuing REM sleep may stabilize transformed memories. While elaborated with respect to hippocampus-dependent memories, the concept of an active redistribution of memory representations from networks serving as temporary store into long-term stores might hold also for non-hippocampus-dependent memory, and even for nonneuronal, i.e., immunological memories, giving rise to the idea that the offline consolidation of memory during sleep represents a principle of long-term memory formation established in quite different physiological systems.
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            Communication between neocortex and hippocampus during sleep in rodents.

            Both neocortical and hippocampal networks organize the firing patterns of their neurons by prominent oscillations during sleep, but the functional role of these rhythms is not well understood. Here, we show a robust correlation of neuronal discharges between the somatosensory cortex and hippocampus on both slow and fine time scales in the mouse and rat. Neuronal bursts in deep cortical layers, associated with sleep spindles and delta waves/slow rhythm, effectively triggered hippocampal discharges related to fast (ripple) oscillations. We hypothesize that oscillation-mediated temporal links coordinate specific information transfer between neocortical and hippocampal cell assemblies. Such a neocortical-hippocampal interplay may be important for memory consolidation.
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              Coordinated interactions between hippocampal ripples and cortical spindles during slow-wave sleep.

              Sleep is characterized by a structured combination of neuronal oscillations. In the hippocampus, slow-wave sleep (SWS) is marked by high-frequency network oscillations (approximately 200 Hz "ripples"), whereas neocortical SWS activity is organized into low-frequency delta (1-4 Hz) and spindle (7-14 Hz) oscillations. While these types of hippocampal and cortical oscillations have been studied extensively in isolation, the relationships between them remain unknown. Here, we demonstrate the existence of temporal correlations between hippocampal ripples and cortical spindles that are also reflected in the correlated activity of single neurons within these brain structures. Spindle-ripple episodes may thus constitute an important mechanism of cortico-hippocampal communication during sleep. This coactivation of hippocampal and neocortical pathways may be important for the process of memory consolidation, during which memories are gradually translated from short-term hippocampal to longer-term neocortical stores.
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                Author and article information

                Journal
                sscus
                SSCUS
                Sleep Spindles & Cortical Up States
                Sleep Spindles & Cortical Up States
                Akadémiai Kiadó (Budapest )
                01 December 2016
                March 2017
                : 1
                : 1
                : 27-41
                Affiliations
                [ 1 ]Center for Advanced Research in Sleep Medicine, CIUSSS-NÎM – Hôpital du Sacré-Coeur de Montréal, Montréal, Québec, Canada
                [ 2 ]Department of Psychiatry, Université de Montréal , Montréal, Québec, Canada
                [ 3 ]Department of Biomedical Sciences, Université de Montréal , Montréal, Québec, Canada
                [ 4 ]Department of Psychology, Université de Montréal , Montréal, Québec, Canada
                [ 5 ]Department of Psychology, Université du Québec à Montréal , Montréal, Québec, Canada
                [ 6 ]Department of Neurosciences, Université de Montréal , Montréal, Québec, Canada
                Author notes
                [* ]Correspondence: Tore Nielsen, Dream & Nightmare Laboratory and Center for Advanced Research in Sleep Medicine, CIUSSS-NÎM – Hôpital du Sacré-Coeur de Montréal, 5400 Gouin Blvd. West, Montréal, Québec H4J 1C5, Canada, E-mail: tore.nielsen@ 123456umontreal.ca
                Article
                10.1556/2053.1.2016.003
                f4c0cdc8-cf51-4ea5-a8e1-dc67eca1a889
                © 2016 The Author(s)

                This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium for non-commercial purposes, provided the original author and source are credited.

                History
                : 07 October 2016
                : 03 November 2016
                : 07 November 2016
                Page count
                Figures: 4, Tables: 7, Equations: 0, References: 98, Pages: 15
                Categories
                ORIGINAL REPORT

                Evolutionary Biology,Medicine,Psychology,Educational research & Statistics,Social & Behavioral Sciences
                N2 sleep,dreaming,REM sleep,sleep spindles,memory consolidation

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