The Case of the Disappearing Spindle Burst

Sleep spindles are brief cortical oscillations at 10–15 Hz that occur predominantly during non-REM (quiet) sleep in adult mammals and are thought to contribute to learning and memory. Spindle bursts are phenomenologically similar to sleep spindles, but they occur predominantly in early infancy and a...

Full description

Saved in:
Bibliographic Details
Main Authors: Alexandre Tiriac, Mark S. Blumberg
Format: Article
Language:English
Published: Wiley 2016-01-01
Series:Neural Plasticity
Online Access:http://dx.doi.org/10.1155/2016/8037321
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1832552463053357056
author Alexandre Tiriac
Mark S. Blumberg
author_facet Alexandre Tiriac
Mark S. Blumberg
author_sort Alexandre Tiriac
collection DOAJ
description Sleep spindles are brief cortical oscillations at 10–15 Hz that occur predominantly during non-REM (quiet) sleep in adult mammals and are thought to contribute to learning and memory. Spindle bursts are phenomenologically similar to sleep spindles, but they occur predominantly in early infancy and are triggered by peripheral sensory activity (e.g., by retinal waves); accordingly, spindle bursts are thought to organize neural networks in the developing brain and establish functional links with the sensory periphery. Whereas the spontaneous retinal waves that trigger spindle bursts in visual cortex are a transient feature of early development, the myoclonic twitches that drive spindle bursts in sensorimotor cortex persist into adulthood. Moreover, twitches—and their associated spindle bursts—occur exclusively during REM (active) sleep. Curiously, despite the persistence of twitching into adulthood, twitch-related spindle bursts have not been reported in adult sensorimotor cortex. This raises the question of whether such spindle burst activity does not occur in adulthood or, alternatively, occurs but has yet to be discovered. If twitch-related spindle bursts do occur in adults, they could contribute to the calibration, maintenance, and repair of sensorimotor systems.
format Article
id doaj-art-d58074babbb84804a2b30507c54ca605
institution Kabale University
issn 2090-5904
1687-5443
language English
publishDate 2016-01-01
publisher Wiley
record_format Article
series Neural Plasticity
spelling doaj-art-d58074babbb84804a2b30507c54ca6052025-02-03T05:58:44ZengWileyNeural Plasticity2090-59041687-54432016-01-01201610.1155/2016/80373218037321The Case of the Disappearing Spindle BurstAlexandre Tiriac0Mark S. Blumberg1Department of Psychological & Brain Sciences, The University of Iowa, Iowa City, IA 52242, USADepartment of Psychological & Brain Sciences, The University of Iowa, Iowa City, IA 52242, USASleep spindles are brief cortical oscillations at 10–15 Hz that occur predominantly during non-REM (quiet) sleep in adult mammals and are thought to contribute to learning and memory. Spindle bursts are phenomenologically similar to sleep spindles, but they occur predominantly in early infancy and are triggered by peripheral sensory activity (e.g., by retinal waves); accordingly, spindle bursts are thought to organize neural networks in the developing brain and establish functional links with the sensory periphery. Whereas the spontaneous retinal waves that trigger spindle bursts in visual cortex are a transient feature of early development, the myoclonic twitches that drive spindle bursts in sensorimotor cortex persist into adulthood. Moreover, twitches—and their associated spindle bursts—occur exclusively during REM (active) sleep. Curiously, despite the persistence of twitching into adulthood, twitch-related spindle bursts have not been reported in adult sensorimotor cortex. This raises the question of whether such spindle burst activity does not occur in adulthood or, alternatively, occurs but has yet to be discovered. If twitch-related spindle bursts do occur in adults, they could contribute to the calibration, maintenance, and repair of sensorimotor systems.http://dx.doi.org/10.1155/2016/8037321
spellingShingle Alexandre Tiriac
Mark S. Blumberg
The Case of the Disappearing Spindle Burst
Neural Plasticity
title The Case of the Disappearing Spindle Burst
title_full The Case of the Disappearing Spindle Burst
title_fullStr The Case of the Disappearing Spindle Burst
title_full_unstemmed The Case of the Disappearing Spindle Burst
title_short The Case of the Disappearing Spindle Burst
title_sort case of the disappearing spindle burst
url http://dx.doi.org/10.1155/2016/8037321
work_keys_str_mv AT alexandretiriac thecaseofthedisappearingspindleburst
AT marksblumberg thecaseofthedisappearingspindleburst
AT alexandretiriac caseofthedisappearingspindleburst
AT marksblumberg caseofthedisappearingspindleburst