fMRI Evidence for Default Mode Network Deactivation Associated with Rapid Eye Movements in Sleep

System-specific brain responses—time-locked to rapid eye movements (REMs) in sleep—are characteristically widespread, with robust and clear activation in the primary visual cortex and other structures involved in multisensory integration. This pattern suggests that REMs underwrite hierarchical processing of visual information in a time-locked manner, where REMs index the generation and scanning of virtual-world models, through multisensory integration in dreaming—as in awake states. Default mode network (DMN) activity increases during rest and reduces during various tasks including visual perception. The implicit anticorrelation between the DMN and task-positive network (TPN)—that persists in REM sleep—prompted us to focus on DMN responses to temporally-precise REM events. We timed REMs during sleep from the video recordings and quantified the neural correlates of REMs—using functional MRI (fMRI)—in 24 independent studies of 11 healthy participants. A reanalysis of these data revealed that the cortical areas exempt from widespread REM-locked brain activation were restricted to the DMN. Furthermore, our analysis revealed a modest temporally-precise REM-locked decrease—phasic deactivation—in key DMN nodes, in a subset of independent studies. These results are consistent with hierarchical predictive coding; namely, permissive deactivation of DMN at the top of the hierarchy (leading to the widespread cortical activation at lower levels; especially the primary visual cortex). Additional findings indicate REM-locked cerebral vasodilation and suggest putative mechanisms for dream forgetting.

End-of-Life in Oncologic Patients’ Dream Content

Both non-rapid eye movements and rapid eye movements sleep facilitate the strengthening of newly encoded memory traces, and dream content reflects this process. Numerous studies evaluated the impact of diseases on dream content, with particular reference to cancer, and reported the presence of issues related to death, negative emotions, pain and illness. This study investigates death and illness experiences in 13 consecutive patients with sarcoma compared to paired controls, early after diagnosis, evaluating dream contents, fear of death, mood and anxiety, distress, and severity of disease perception (perceived and communicated). Ten patients and 10 controls completed the study. Dream contents were significantly different between patients and normative data (DreamSat) and patients and controls (higher presence of negative emotions, low familiar settings and characters and no success involving the dreamer). Illness and death were present in 57% of patients’ dreams (0% among controls), but no differences emerged between patients and controls in regard to anxiety and depression, distress and fear of death, even if the severity of illness was correctly perceived. The appearance of emotional elements in dreams and the absence of conscious verbalization of distress and/or depressive or anxious symptoms by patients could be ascribed to the time required for mnestic elaboration (construction/elaboration phase) during sleep.

Neurons in the Nucleus papilio contribute to the control of eye movements during REM sleep

Rapid eye movements (REM) are characteristic of the eponymous phase of sleep, yet the underlying motor commands remain an enigma. Here, we identified a cluster of Calbindin-D28K-expressing neurons in the Nucleus papilio (NPCalb), located in the dorsal paragigantocellular nucleus, which are active during REM sleep and project to the three contralateral eye-muscle nuclei. The firing of opto-tagged NPCalb neurons is augmented prior to the onset of eye movements during REM sleep. Optogenetic activation of NPCalb neurons triggers eye movements selectively during REM sleep, while their genetic ablation or optogenetic silencing suppresses them. None of these perturbations led to a change in the duration of REM sleep episodes. Our study provides the first evidence for a brainstem premotor command contributing to the control of eye movements selectively during REM sleep in the mammalian brain.

Tachyons but Not Photons Might Generate Conscious Dreams

We had learnt from cognitive vision that involuntarily visual awareness should be generated by exogenous stimuli; but not indigenous! Given the complexity of understanding the reasons behind the rapid eye movements during vivid dreams; dreams that carry highly bizarre information; dreams that disallow the human subjects to have control over what they see; these types of dreams should be therefore reside under the umbrella of the “involuntary human awareness”. We therefore suggest possibilities of physical particles that could carry the visual information of these extraordinary exogenous stimuli; particles that should be able to invade the human’s eyes while they are closed; particles that have the ability to move the eye rapidly aiming for perfect transformation of the visual information. The present research aims to talk about these particles, proposes scenarios of how human eye & retina deal with them.

Night watch during REM sleep for the first-night effect

ABSTRACTWe experience disturbed sleep in a new place, and this effect is known as the first-night effect (FNE) in sleep research. We previously demonstrated that the FNE was associated with a protective night-watch system during NREM sleep in one hemisphere, which is shown as interhemispheric asymmetry in sleep depth in the default-mode network (DMN), and interhemispheric asymmetry in increased vigilance to monitor external stimuli. The present study investigated whether rapid eye movement (REM) sleep exhibited a form similar to a night-watch system during NREM sleep. First, we tested whether theta activity, which is an index of the depth of REM sleep, showed interhemispheric asymmetry in association with the FNE, by source-localizing to the DMN. However, interhemispheric asymmetry in theta activity during REM sleep was not found in association with the FNE. Next, we tested whether vigilance, as measured by evoked brain responses to deviant sounds, was increased in one hemisphere and showed interhemispheric asymmetry in association with the FNE during REM sleep. Because vigilance is different between the phasic period where rapid eye movements occur and the tonic period where rapid eye movements do not occur during REM sleep, REM sleep was split into phasic and tonic periods for measurements of evoked brain responses. While the evoked brain responses are generally small during the phasic period without the FNE, we found that the evoked brain response was significantly augmented by the FNE during the phasic period. In contrast, the evoked brain response during the tonic period did not differ by the presence of the FNE. Interhemispheric asymmetry in brain responses was not found during the phasic or tonic periods. These results suggest that a night-watch system for the FNE appears as interhemispheric asymmetry in sleep depth and vigilance during NREM sleep, but it appears as increased vigilance in both hemispheres during the phasic period, when vigilance to external stimuli is generally reduced without the FNE, during REM sleep. Therefore, a night-watch system associated with the FNE may be subserved by different neural mechanisms during NREM and REM sleep.