Long term effects of cueing procedural memory reactivation during NREM sleep
•A single night of TMR benefits procedural memories up to 10 days later.•Spindle density and SO-spindle coupling strength increase immediately upon cue onset.•Time spent in N2 but not N3 predicts cueing benefit. Targeted memory reactivation (TMR) has recently emerged as a promising tool to manipulat...
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Published in | NeuroImage (Orlando, Fla.) Vol. 244; p. 118573 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
United States
Elsevier Inc
01.12.2021
Elsevier Limited Academic Press Elsevier |
Subjects | |
Online Access | Get full text |
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Summary: | •A single night of TMR benefits procedural memories up to 10 days later.•Spindle density and SO-spindle coupling strength increase immediately upon cue onset.•Time spent in N2 but not N3 predicts cueing benefit.
Targeted memory reactivation (TMR) has recently emerged as a promising tool to manipulate and study the sleeping brain. Although the technique is developing rapidly, only a few studies have examined how the effects of TMR develop over time. Here, we use a bimanual serial reaction time task (SRTT) to investigate whether the difference between the cued and un-cued sequence of button presses persists long-term. We further explore the relationship between the TMR benefit and sleep spindles, as well as their coupling with slow oscillations. Our behavioural analysis shows better performance for the dominant hand. Importantly, there was a strong effect of TMR, with improved performance on the cued sequence after sleep. Closer examination revealed a significant benefit of TMR at 10 days post-encoding, but not 24 h or 6 weeks post-encoding. Time spent in stage 2, but not stage 3, of NREM sleep predicted cueing benefit. We also found a significant increase in spindle density and SO-spindle coupling during the cue period, when compared to the no-cue period. Together, our results demonstrate that TMR effects evolve over several weeks post-cueing, as well as emphasising the importance of stage 2, spindles and the SO-spindle coupling in procedural memory consolidation. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 Present address: Experimental Psychopathology Lab, Institute of Psychology, Polish Academy of Sciences, Warsaw, Poland. Present address: Department of Biomedical Engineering, Universidad de los Andes, Bogotá, Colombia. |
ISSN: | 1053-8119 1095-9572 |
DOI: | 10.1016/j.neuroimage.2021.118573 |