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Regulation of cortical activity and arousal by the matrix cells of the ventromedial thalamic nucleus
by
Nagai, Hirotaka
, Honjoh, Sakiko
, Tononi, Giulio
, Cirelli, Chiara
, Sasai, Shuntaro
, Schiereck, Shannon S
in
59
/ 631/378/1385/1814
/ 631/378/1385/1877
/ 631/378/1385/519
/ 64
/ 64/60
/ Activation
/ Anesthesia
/ Animals
/ Arousal
/ Calbindins - metabolism
/ Cerebral Cortex - cytology
/ Cerebral Cortex - physiology
/ Cortex
/ Humanities and Social Sciences
/ Male
/ Mice
/ Mice, Inbred C57BL
/ multidisciplinary
/ NREM sleep
/ Nuclei (cytology)
/ REM sleep
/ Science
/ Science (multidisciplinary)
/ Sleep
/ Sleep and wakefulness
/ Sleep, REM - physiology
/ Sleep, Slow-Wave - physiology
/ Thalamic nuclei
/ Thalamus
/ Ventral Thalamic Nuclei - cytology
/ Ventral Thalamic Nuclei - physiology
/ Wakefulness - physiology
2018
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Regulation of cortical activity and arousal by the matrix cells of the ventromedial thalamic nucleus
by
Nagai, Hirotaka
, Honjoh, Sakiko
, Tononi, Giulio
, Cirelli, Chiara
, Sasai, Shuntaro
, Schiereck, Shannon S
in
59
/ 631/378/1385/1814
/ 631/378/1385/1877
/ 631/378/1385/519
/ 64
/ 64/60
/ Activation
/ Anesthesia
/ Animals
/ Arousal
/ Calbindins - metabolism
/ Cerebral Cortex - cytology
/ Cerebral Cortex - physiology
/ Cortex
/ Humanities and Social Sciences
/ Male
/ Mice
/ Mice, Inbred C57BL
/ multidisciplinary
/ NREM sleep
/ Nuclei (cytology)
/ REM sleep
/ Science
/ Science (multidisciplinary)
/ Sleep
/ Sleep and wakefulness
/ Sleep, REM - physiology
/ Sleep, Slow-Wave - physiology
/ Thalamic nuclei
/ Thalamus
/ Ventral Thalamic Nuclei - cytology
/ Ventral Thalamic Nuclei - physiology
/ Wakefulness - physiology
2018
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Regulation of cortical activity and arousal by the matrix cells of the ventromedial thalamic nucleus
by
Nagai, Hirotaka
, Honjoh, Sakiko
, Tononi, Giulio
, Cirelli, Chiara
, Sasai, Shuntaro
, Schiereck, Shannon S
in
59
/ 631/378/1385/1814
/ 631/378/1385/1877
/ 631/378/1385/519
/ 64
/ 64/60
/ Activation
/ Anesthesia
/ Animals
/ Arousal
/ Calbindins - metabolism
/ Cerebral Cortex - cytology
/ Cerebral Cortex - physiology
/ Cortex
/ Humanities and Social Sciences
/ Male
/ Mice
/ Mice, Inbred C57BL
/ multidisciplinary
/ NREM sleep
/ Nuclei (cytology)
/ REM sleep
/ Science
/ Science (multidisciplinary)
/ Sleep
/ Sleep and wakefulness
/ Sleep, REM - physiology
/ Sleep, Slow-Wave - physiology
/ Thalamic nuclei
/ Thalamus
/ Ventral Thalamic Nuclei - cytology
/ Ventral Thalamic Nuclei - physiology
/ Wakefulness - physiology
2018
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Regulation of cortical activity and arousal by the matrix cells of the ventromedial thalamic nucleus
Journal Article
Regulation of cortical activity and arousal by the matrix cells of the ventromedial thalamic nucleus
2018
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Overview
The “non-specific” ventromedial thalamic nucleus (VM) has long been considered a candidate for mediating cortical arousal due to its diffuse, superficial projections, but direct evidence was lacking. Here, we show in mice that the activity of VM calbindin1-positive matrix cells is high in wake and REM sleep and low in NREM sleep, and increases before cortical activity at the sleep-to-wake transition. Optogenetic stimulation of VM cells rapidly awoke all mice from NREM sleep and consistently caused EEG activation during slow wave anesthesia, while arousal did not occur from REM sleep. Conversely, chemogenetic inhibition of VM decreased wake duration. Optogenetic activation of the “specific” ventral posteromedial nucleus (VPM) did not cause arousal from either NREM or REM sleep. Thus, matrix cells in VM produce arousal and broad cortical activation during NREM sleep and slow wave anesthesia in a way that accounts for the effects classically attributed to “non-specific” thalamic nuclei.
The ventromedial thalamus (VM) is thought to control cortical arousal through its diffuse projections to cortex. Here the authors record and manipulate the activity of calbindin1-positive matrix cells in VM and show that they bidirectionally regulate the sleep-wake transition.
Publisher
Nature Publishing Group UK,Nature Publishing Group,Nature Portfolio
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