Abstract

The human electroencephalogram (EEG) during non-rapid eye movement sleep (NREM) is characterized mainly by high-amplitude (>75 μV), slow-frequency (<4 Hz) waves (slow waves), and sleep spindles (∼11–15 Hz; >0.25 s). These NREM oscillations play a crucial role in brain plasticity, and importantly, NREM sleep oscillations change considerably with aging. This review discusses the association between NREM sleep oscillations and cerebral plasticity as well as the functional impact of age-related changes on NREM sleep oscillations. We propose that age-related reduction in sleep-dependent memory consolidation may be due in part to changes in NREM sleep oscillations.

Highlights

  • SLOW-WAVE NREM SLEEP OSCILLATIONS Non-rapid eye movement (NREM) sleep is characterized by different degrees of cortical synchronization, from lower in lighter sleep stages (1 and 2) to higher in deeper slow-wave sleep (SWS) stages

  • slow-wave activity (SWA) and memory performance in healthy elderly patients, by experimentally reducing SWA using acoustic neurofeedback. This procedure was found to decrease the encoding of novel declarative information in older subjects (Van Der Werf et al, 2011). These results suggest that NREM sleep spindles and SWA are related to declarative memory encoding and retention in older adults

  • NREM sleep oscillations are related to the reactivation of recently learned material, cerebral plasticity, and synaptic homeostasis

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Summary

Introduction

SLOW-WAVE NREM SLEEP OSCILLATIONS Non-rapid eye movement (NREM) sleep is characterized by different degrees of cortical synchronization, from lower in lighter sleep stages (1 and 2) to higher in deeper slow-wave sleep (SWS) stages. This age-related reduction in slow activity during NREM sleep may have a negative impact on brain plasticity and sleep-dependent memory consolidation. In addition to reduced SW during NREM sleep, spindle density, amplitude, and duration are reduced in older compared to young subjects (Guazzelli et al, 1986; Wei et al, 1999; Crowley et al, 2002), and this decline has been shown to be progressive with age (Principe and Smith, 1982; Nicolas et al, 2001).

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