Predicting Dream Recall: EEG Activation During NREM Sleep or Shared Mechanisms with Wakefulness?

Dream recall upon awakening from NREM sleep is predicted by reduced delta activity in left frontal and temporo-parietal areas during the final segment of sleep. This finding suggests that increased cortical activation is a prerequisite for remembering dreams from NREM sleep, challenging the traditional view that dreaming is unique to REM sleep. The study used a multiple nap protocol and within-subjects design to collect dream reports after stage 2 NREM sleep awakenings. The results indicate that the brain mechanisms underlying dream recall during NREM sleep may share features with those involved in encoding episodic memories during wakefulness, though they also depend on the specific electrophysiological state of sleep.

Study at a glance

Abstract

The common knowledge of a uniqueness of REM sleep as a privileged scenario of dreaming still persists, although consolidated empirical evidence shows that the assumption that dreaming is just an epiphenomenon of REM sleep is no longer tenable. However, the brain mechanisms underlying dream generation and its encoding in memory during NREM sleep are still mostly unknown. In fact, only few studies have investigated on the mechanisms of dream phenomenology related to NREM sleep. For this reason, our study is specifically aimed to elucidate the electrophysiological (EEG) correlates of dream recall (DR) upon NREM sleep awakenings. Under the assumption that EEG activity predicts the presence/absence of DR also during NREM sleep, we have investigated whether DR from stage 2 NREM sleep shares similar brain mechanisms to those involved in the encoding of episodic memory during wakefulness, or it depends on the specific electrophysiological milieu of the sleep period along the desynchronized/synchronized EEG continuum. We collected DR from a multiple nap protocol in a within-subjects design. We found that DR is predicted by an extensive reduction of delta activity during the last segment of sleep, encompassing left frontal and temporo-parietal areas. The results could represent an update on the mechanisms underlying the sleep mentation during NREM sleep. In particular, they support the hypothesis that an increased cortical EEG activation is a prerequisite for DR, and they are not necessarily in conflict with the hypothesis of common wake-sleep mechanisms. We also confirmed that EEG correlates of DR depend on a state-like relationship.