Cargando…

Selectively driving cholinergic fibers optically in the thalamic reticular nucleus promotes sleep

Cholinergic projections from the basal forebrain and brainstem are thought to play important roles in rapid eye movement (REM) sleep and arousal. Using transgenic mice in which channelrhdopsin-2 is selectively expressed in cholinergic neurons, we show that optical stimulation of cholinergic inputs t...

Descripción completa

Detalles Bibliográficos
Autores principales: Ni, Kun-Ming, Hou, Xiao-Jun, Yang, Ci-Hang, Dong, Ping, Li, Yue, Zhang, Ying, Jiang, Ping, Berg, Darwin K, Duan, Shumin, Li, Xiao-Ming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4764559/
https://www.ncbi.nlm.nih.gov/pubmed/26880556
http://dx.doi.org/10.7554/eLife.10382
_version_ 1782417391672623104
author Ni, Kun-Ming
Hou, Xiao-Jun
Yang, Ci-Hang
Dong, Ping
Li, Yue
Zhang, Ying
Jiang, Ping
Berg, Darwin K
Duan, Shumin
Li, Xiao-Ming
author_facet Ni, Kun-Ming
Hou, Xiao-Jun
Yang, Ci-Hang
Dong, Ping
Li, Yue
Zhang, Ying
Jiang, Ping
Berg, Darwin K
Duan, Shumin
Li, Xiao-Ming
author_sort Ni, Kun-Ming
collection PubMed
description Cholinergic projections from the basal forebrain and brainstem are thought to play important roles in rapid eye movement (REM) sleep and arousal. Using transgenic mice in which channelrhdopsin-2 is selectively expressed in cholinergic neurons, we show that optical stimulation of cholinergic inputs to the thalamic reticular nucleus (TRN) activates local GABAergic neurons to promote sleep and protect non-rapid eye movement (NREM) sleep. It does not affect REM sleep. Instead, direct activation of cholinergic input to the TRN shortens the time to sleep onset and generates spindle oscillations that correlate with NREM sleep. It does so by evoking excitatory postsynaptic currents via α7-containing nicotinic acetylcholine receptors and inducing bursts of action potentials in local GABAergic neurons. These findings stand in sharp contrast to previous reports of cholinergic activity driving arousal. Our results provide new insight into the mechanisms controlling sleep. DOI: http://dx.doi.org/10.7554/eLife.10382.001
format Online
Article
Text
id pubmed-4764559
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher eLife Sciences Publications, Ltd
record_format MEDLINE/PubMed
spelling pubmed-47645592016-02-25 Selectively driving cholinergic fibers optically in the thalamic reticular nucleus promotes sleep Ni, Kun-Ming Hou, Xiao-Jun Yang, Ci-Hang Dong, Ping Li, Yue Zhang, Ying Jiang, Ping Berg, Darwin K Duan, Shumin Li, Xiao-Ming eLife Cell Biology Cholinergic projections from the basal forebrain and brainstem are thought to play important roles in rapid eye movement (REM) sleep and arousal. Using transgenic mice in which channelrhdopsin-2 is selectively expressed in cholinergic neurons, we show that optical stimulation of cholinergic inputs to the thalamic reticular nucleus (TRN) activates local GABAergic neurons to promote sleep and protect non-rapid eye movement (NREM) sleep. It does not affect REM sleep. Instead, direct activation of cholinergic input to the TRN shortens the time to sleep onset and generates spindle oscillations that correlate with NREM sleep. It does so by evoking excitatory postsynaptic currents via α7-containing nicotinic acetylcholine receptors and inducing bursts of action potentials in local GABAergic neurons. These findings stand in sharp contrast to previous reports of cholinergic activity driving arousal. Our results provide new insight into the mechanisms controlling sleep. DOI: http://dx.doi.org/10.7554/eLife.10382.001 eLife Sciences Publications, Ltd 2016-02-11 /pmc/articles/PMC4764559/ /pubmed/26880556 http://dx.doi.org/10.7554/eLife.10382 Text en © 2016, Ni et al http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Cell Biology
Ni, Kun-Ming
Hou, Xiao-Jun
Yang, Ci-Hang
Dong, Ping
Li, Yue
Zhang, Ying
Jiang, Ping
Berg, Darwin K
Duan, Shumin
Li, Xiao-Ming
Selectively driving cholinergic fibers optically in the thalamic reticular nucleus promotes sleep
title Selectively driving cholinergic fibers optically in the thalamic reticular nucleus promotes sleep
title_full Selectively driving cholinergic fibers optically in the thalamic reticular nucleus promotes sleep
title_fullStr Selectively driving cholinergic fibers optically in the thalamic reticular nucleus promotes sleep
title_full_unstemmed Selectively driving cholinergic fibers optically in the thalamic reticular nucleus promotes sleep
title_short Selectively driving cholinergic fibers optically in the thalamic reticular nucleus promotes sleep
title_sort selectively driving cholinergic fibers optically in the thalamic reticular nucleus promotes sleep
topic Cell Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4764559/
https://www.ncbi.nlm.nih.gov/pubmed/26880556
http://dx.doi.org/10.7554/eLife.10382
work_keys_str_mv AT nikunming selectivelydrivingcholinergicfibersopticallyinthethalamicreticularnucleuspromotessleep
AT houxiaojun selectivelydrivingcholinergicfibersopticallyinthethalamicreticularnucleuspromotessleep
AT yangcihang selectivelydrivingcholinergicfibersopticallyinthethalamicreticularnucleuspromotessleep
AT dongping selectivelydrivingcholinergicfibersopticallyinthethalamicreticularnucleuspromotessleep
AT liyue selectivelydrivingcholinergicfibersopticallyinthethalamicreticularnucleuspromotessleep
AT zhangying selectivelydrivingcholinergicfibersopticallyinthethalamicreticularnucleuspromotessleep
AT jiangping selectivelydrivingcholinergicfibersopticallyinthethalamicreticularnucleuspromotessleep
AT bergdarwink selectivelydrivingcholinergicfibersopticallyinthethalamicreticularnucleuspromotessleep
AT duanshumin selectivelydrivingcholinergicfibersopticallyinthethalamicreticularnucleuspromotessleep
AT lixiaoming selectivelydrivingcholinergicfibersopticallyinthethalamicreticularnucleuspromotessleep