Lesion of intergeniculate leaflet GABAergic neurons attenuates sleep in mice exposed to light
Abstract Light has immediate effects on sleep in rodents, but the neural pathways underlying the effect remain to be elucidated. The intergeniculate leaflet (IGL) containing GABAergic neurons receives direct retinal inputs. We hypothesized that IGL GABAergic neurons may mediate light-induced sleep....
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Veröffentlicht in: | Sleep (New York, N.Y.) N.Y.), 2020-02, Vol.43 (2), p.1 |
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description | Abstract
Light has immediate effects on sleep in rodents, but the neural pathways underlying the effect remain to be elucidated. The intergeniculate leaflet (IGL) containing GABAergic neurons receives direct retinal inputs. We hypothesized that IGL GABAergic neurons may mediate light-induced sleep. EEG/electromyogram recording, immunohistochemistry, electrophysiology, optogenetics, fiber photometry, behavioral tests, and cell-specific destruction were employed to investigate the role of IGL GABAergic neurons in the regulation of acute light-induced sleep. Here, EEG/electromyogram recordings revealed that acute light exposure during the nocturnal active phase in mice induced a significant increase in non-rapid eye movement and rapid eye movement sleep compared with controls. Immunohistochemistry showed that acute light exposure for 2 hours in the active phase induced an increase in c-Fos expression in the IGL, whereas lights-off in the rest phase inhibited it. Patch clamp coupled with optogenetics demonstrated that retinal ganglion cells had monosynaptic functional connections to IGL GABAergic neurons. Calcium activity by fiber photometry in freely behaving mice showed that light exposure increased the activity of IGL GABAergic neurons. Furthermore, lesion of IGL GABAergic neurons by caspase-3 virus significantly attenuated the sleep-promoting effect of light exposure during active phases. Collectively, these results clearly indicated that the IGL is one of key nuclei mediating light-induced sleep in mice. |
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Light has immediate effects on sleep in rodents, but the neural pathways underlying the effect remain to be elucidated. The intergeniculate leaflet (IGL) containing GABAergic neurons receives direct retinal inputs. We hypothesized that IGL GABAergic neurons may mediate light-induced sleep. EEG/electromyogram recording, immunohistochemistry, electrophysiology, optogenetics, fiber photometry, behavioral tests, and cell-specific destruction were employed to investigate the role of IGL GABAergic neurons in the regulation of acute light-induced sleep. Here, EEG/electromyogram recordings revealed that acute light exposure during the nocturnal active phase in mice induced a significant increase in non-rapid eye movement and rapid eye movement sleep compared with controls. Immunohistochemistry showed that acute light exposure for 2 hours in the active phase induced an increase in c-Fos expression in the IGL, whereas lights-off in the rest phase inhibited it. Patch clamp coupled with optogenetics demonstrated that retinal ganglion cells had monosynaptic functional connections to IGL GABAergic neurons. Calcium activity by fiber photometry in freely behaving mice showed that light exposure increased the activity of IGL GABAergic neurons. Furthermore, lesion of IGL GABAergic neurons by caspase-3 virus significantly attenuated the sleep-promoting effect of light exposure during active phases. Collectively, these results clearly indicated that the IGL is one of key nuclei mediating light-induced sleep in mice.</description><identifier>ISSN: 0161-8105</identifier><identifier>EISSN: 1550-9109</identifier><identifier>DOI: 10.1093/sleep/zsz212</identifier><identifier>PMID: 31552427</identifier><language>eng</language><publisher>US: Oxford University Press</publisher><subject>Animals ; Circadian Rhythm ; Comparative analysis ; Eye movements ; GABA ; GABAergic Neurons ; Geniculate Bodies ; Health aspects ; Immunohistochemistry ; Light ; Mice ; Neurons ; Proto-Oncogene Proteins c-fos ; Rats ; Rats, Wistar ; REM sleep ; Sleep ; Sleep disorders ; Suprachiasmatic Nucleus</subject><ispartof>Sleep (New York, N.Y.), 2020-02, Vol.43 (2), p.1</ispartof><rights>Sleep Research Society 2019. Published by Oxford University Press on behalf of the Sleep Research Society. All rights reserved. For permissions, please e-mail journals.permissions@oup.com. 2019</rights><rights>Sleep Research Society 2019. Published by Oxford University Press on behalf of the Sleep Research Society. All rights reserved. For permissions, please e-mail journals.permissions@oup.com.</rights><rights>COPYRIGHT 2020 Oxford University Press</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4732-95c27db94bc7f45ba45206c62b41d27f10fb2240d70c8221b683186a4069a2563</citedby><cites>FETCH-LOGICAL-c4732-95c27db94bc7f45ba45206c62b41d27f10fb2240d70c8221b683186a4069a2563</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,1578,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31552427$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Shi, Huan-Ying</creatorcontrib><creatorcontrib>Xu, Wei</creatorcontrib><creatorcontrib>Guo, Han</creatorcontrib><creatorcontrib>Dong, Hui</creatorcontrib><creatorcontrib>Qu, Wei-Min</creatorcontrib><creatorcontrib>Huang, Zhi-Li</creatorcontrib><title>Lesion of intergeniculate leaflet GABAergic neurons attenuates sleep in mice exposed to light</title><title>Sleep (New York, N.Y.)</title><addtitle>Sleep</addtitle><description>Abstract
Light has immediate effects on sleep in rodents, but the neural pathways underlying the effect remain to be elucidated. The intergeniculate leaflet (IGL) containing GABAergic neurons receives direct retinal inputs. We hypothesized that IGL GABAergic neurons may mediate light-induced sleep. EEG/electromyogram recording, immunohistochemistry, electrophysiology, optogenetics, fiber photometry, behavioral tests, and cell-specific destruction were employed to investigate the role of IGL GABAergic neurons in the regulation of acute light-induced sleep. Here, EEG/electromyogram recordings revealed that acute light exposure during the nocturnal active phase in mice induced a significant increase in non-rapid eye movement and rapid eye movement sleep compared with controls. Immunohistochemistry showed that acute light exposure for 2 hours in the active phase induced an increase in c-Fos expression in the IGL, whereas lights-off in the rest phase inhibited it. Patch clamp coupled with optogenetics demonstrated that retinal ganglion cells had monosynaptic functional connections to IGL GABAergic neurons. Calcium activity by fiber photometry in freely behaving mice showed that light exposure increased the activity of IGL GABAergic neurons. Furthermore, lesion of IGL GABAergic neurons by caspase-3 virus significantly attenuated the sleep-promoting effect of light exposure during active phases. Collectively, these results clearly indicated that the IGL is one of key nuclei mediating light-induced sleep in mice.</description><subject>Animals</subject><subject>Circadian Rhythm</subject><subject>Comparative analysis</subject><subject>Eye movements</subject><subject>GABA</subject><subject>GABAergic Neurons</subject><subject>Geniculate Bodies</subject><subject>Health aspects</subject><subject>Immunohistochemistry</subject><subject>Light</subject><subject>Mice</subject><subject>Neurons</subject><subject>Proto-Oncogene Proteins c-fos</subject><subject>Rats</subject><subject>Rats, Wistar</subject><subject>REM sleep</subject><subject>Sleep</subject><subject>Sleep disorders</subject><subject>Suprachiasmatic Nucleus</subject><issn>0161-8105</issn><issn>1550-9109</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>8G5</sourceid><sourceid>BENPR</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNp9kc9rFDEUx4Modq3ePEvAgx6cNr9n57gWW4UFL3qUkMm8rCnZZEwyoP3rzXZbRRHJISTv877fx_si9JySM0oGfl4CwHx-U24YZQ_QikpJuqFVHqIVoYp2a0rkCXpSyjVpbzHwx-iEN4oJ1q_Qly0UnyJODvtYIe8gersEUwEHMC5AxVebt5tW8BZHWHKKBZtaIS6NKfjWvbXivbeA4fucCky4Jhz87mt9ih45Ewo8u7tP0efLd58u3nfbj1cfLjbbzoqes26QlvXTOIjR9k7I0QjJiLKKjYJOrHeUuJExQaae2DVjdFRrTtfKCKIGw6Tip-j1UXfO6dsCpeq9LxZCMBHSUjRjQ0-ZpL1s6Mu_0Ou05Nim00xwSpoNIb-pnQmgfXSpZmMPonqjBCeK8-Fge_YPqp0J2jpSBOfb_x8Nb44NNqdSMjg9Z783-YemRB_S1Lf71Mc0G_7ibtZl3MP0C76PrwGvjkBa5v9L_QSQcqbn</recordid><startdate>20200201</startdate><enddate>20200201</enddate><creator>Shi, Huan-Ying</creator><creator>Xu, Wei</creator><creator>Guo, Han</creator><creator>Dong, Hui</creator><creator>Qu, Wei-Min</creator><creator>Huang, Zhi-Li</creator><general>Oxford University Press</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88G</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>M2M</scope><scope>M2O</scope><scope>MBDVC</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PSYQQ</scope><scope>Q9U</scope><scope>7X8</scope></search><sort><creationdate>20200201</creationdate><title>Lesion of intergeniculate leaflet GABAergic neurons attenuates sleep in mice exposed to light</title><author>Shi, Huan-Ying ; Xu, Wei ; Guo, Han ; Dong, Hui ; Qu, Wei-Min ; Huang, Zhi-Li</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4732-95c27db94bc7f45ba45206c62b41d27f10fb2240d70c8221b683186a4069a2563</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Animals</topic><topic>Circadian Rhythm</topic><topic>Comparative analysis</topic><topic>Eye movements</topic><topic>GABA</topic><topic>GABAergic Neurons</topic><topic>Geniculate Bodies</topic><topic>Health aspects</topic><topic>Immunohistochemistry</topic><topic>Light</topic><topic>Mice</topic><topic>Neurons</topic><topic>Proto-Oncogene Proteins c-fos</topic><topic>Rats</topic><topic>Rats, Wistar</topic><topic>REM sleep</topic><topic>Sleep</topic><topic>Sleep disorders</topic><topic>Suprachiasmatic Nucleus</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Shi, Huan-Ying</creatorcontrib><creatorcontrib>Xu, Wei</creatorcontrib><creatorcontrib>Guo, Han</creatorcontrib><creatorcontrib>Dong, Hui</creatorcontrib><creatorcontrib>Qu, Wei-Min</creatorcontrib><creatorcontrib>Huang, Zhi-Li</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Psychology Database (Alumni)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Psychology Database</collection><collection>Research Library</collection><collection>Research Library (Corporate)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest One Psychology</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><jtitle>Sleep (New York, N.Y.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Shi, Huan-Ying</au><au>Xu, Wei</au><au>Guo, Han</au><au>Dong, Hui</au><au>Qu, Wei-Min</au><au>Huang, Zhi-Li</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Lesion of intergeniculate leaflet GABAergic neurons attenuates sleep in mice exposed to light</atitle><jtitle>Sleep (New York, N.Y.)</jtitle><addtitle>Sleep</addtitle><date>2020-02-01</date><risdate>2020</risdate><volume>43</volume><issue>2</issue><spage>1</spage><pages>1-</pages><issn>0161-8105</issn><eissn>1550-9109</eissn><abstract>Abstract
Light has immediate effects on sleep in rodents, but the neural pathways underlying the effect remain to be elucidated. The intergeniculate leaflet (IGL) containing GABAergic neurons receives direct retinal inputs. We hypothesized that IGL GABAergic neurons may mediate light-induced sleep. EEG/electromyogram recording, immunohistochemistry, electrophysiology, optogenetics, fiber photometry, behavioral tests, and cell-specific destruction were employed to investigate the role of IGL GABAergic neurons in the regulation of acute light-induced sleep. Here, EEG/electromyogram recordings revealed that acute light exposure during the nocturnal active phase in mice induced a significant increase in non-rapid eye movement and rapid eye movement sleep compared with controls. Immunohistochemistry showed that acute light exposure for 2 hours in the active phase induced an increase in c-Fos expression in the IGL, whereas lights-off in the rest phase inhibited it. Patch clamp coupled with optogenetics demonstrated that retinal ganglion cells had monosynaptic functional connections to IGL GABAergic neurons. Calcium activity by fiber photometry in freely behaving mice showed that light exposure increased the activity of IGL GABAergic neurons. Furthermore, lesion of IGL GABAergic neurons by caspase-3 virus significantly attenuated the sleep-promoting effect of light exposure during active phases. Collectively, these results clearly indicated that the IGL is one of key nuclei mediating light-induced sleep in mice.</abstract><cop>US</cop><pub>Oxford University Press</pub><pmid>31552427</pmid><doi>10.1093/sleep/zsz212</doi><oa>free_for_read</oa></addata></record> |
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subjects | Animals Circadian Rhythm Comparative analysis Eye movements GABA GABAergic Neurons Geniculate Bodies Health aspects Immunohistochemistry Light Mice Neurons Proto-Oncogene Proteins c-fos Rats Rats, Wistar REM sleep Sleep Sleep disorders Suprachiasmatic Nucleus |
title | Lesion of intergeniculate leaflet GABAergic neurons attenuates sleep in mice exposed to light |
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