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1.
Curr Top Med Chem ; 11(19): 2403-13, 2011.
Article in English | MEDLINE | ID: mdl-21906024

ABSTRACT

Reciprocal interactions between wakefulness and sleep substantially influence human brain function in both states of vigilance. On the one hand, there is evidence that regionally-specialized brain activity during wakefulness is modulated by the interaction between a local use-dependent buildup of homeostatic sleep pressure and circadian signals. On the other hand, brain activity during sleep, although mainly constrained by genuine sleep oscillations, shows wake-dependent regionally-specific modulations, which are involved in the dissipation of local homeostatic sleep pressure and memory consolidation.


Subject(s)
Brain/physiology , Sleep/physiology , Wakefulness/physiology , Animals , Humans
2.
Prog Brain Res ; 193: 111-8, 2011.
Article in English | MEDLINE | ID: mdl-21854959

ABSTRACT

Recent neuroimaging studies characterized the neural correlates of slow waves and spindles during human non-rapid eye movement (NREM) sleep. They showed that significant activity was consistently associated with slow (> 140 µV) and delta waves (75-140 µV) during NREM sleep in several cortical areas including inferior frontal, medial prefrontal, precuneus, and posterior cingulate cortices. Unexpectedly, slow waves were also associated with transient responses in the pontine tegmentum and in the cerebellum. On the other hand, spindles were associated with a transient activity in the thalami, paralimbic areas (anterior cingulate and insular cortices), and superior temporal gyri. Moreover, slow spindles (11-13 Hz) were associated with increased activity in the superior frontal gyrus. In contrast, fast spindles (13-15 Hz) recruited a set of cortical regions involved in sensorimotor processing, as well as the mesial frontal cortex and hippocampus. These findings indicate that human NREM sleep is an active state during which brain activity is temporally organized by spontaneous oscillations (spindles and slow oscillation) in a regionally specific manner. The functional significance of these NREM sleep oscillations is currently interpreted in terms of synaptic homeostasis and memory consolidation.


Subject(s)
Brain/physiology , Neurons/physiology , Sleep Stages/physiology , Brain/anatomy & histology , Electroencephalography , Homeostasis/physiology , Humans , Magnetic Resonance Imaging , Wakefulness/physiology
3.
Biol Aujourdhui ; 204(2): 139-43, 2010.
Article in French | MEDLINE | ID: mdl-20950558

ABSTRACT

A growing body of evidence indicates that sleep promotes memory consolidation. Although the first experimental evidence for this positive influence of sleep on memory was collected more than a century ago, the potential underlying neural mechanisms begins only to be conceptualized and experimentally characterized. A first hypothesis contrasted the influence of non-rapid eye movement (NREM) sleep and rapid eye movement (REM) sleep on declarative and procedural memories, respectively. As the understanding of the effects of sleep on memory consolidation during sleep progressed, the hypotheses were increasingly framed in terms of neural processes occurring with NREM and REM sleep, especially associated with phasic events such as slow waves, spindles or phasic REM sleep. This paper reviews two of these hypotheses: the synaptic downscaling and the systemic consolidation during non NREM sleep.


Subject(s)
Learning/physiology , Memory/physiology , Sleep/physiology , Synapses/physiology , Humans , Sleep Stages/physiology , Sleep, REM/physiology
4.
Int Rev Neurobiol ; 92: 87-99, 2010.
Article in English | MEDLINE | ID: mdl-20870064

ABSTRACT

During the last two decades, functional neuroimaging has been used to characterize the regional brain function during sleep in humans, at the macroscopic systems level. In addition, the topography of brain activity, especially during rapid eye movement sleep, was thought to be compatible with the general features of dreams. In contrast, the neural correlates of dreams remain largely unexplored. This review examines the difficulties associated with the characterization of dream correlates. ἓν οἶδα ὅτι οὐδὲν οἶδα Σωκράτης (The only thing I know is that I know nothing) Socrates.


Subject(s)
Diagnostic Imaging/methods , Dreams/physiology , Evoked Potentials/physiology , Sleep, REM/physiology , Brain/anatomy & histology , Brain/physiology , Diagnostic Imaging/standards , Dreams/psychology , Humans
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