Activation of Parabrachial Nucleus Glutamatergic Neurons Accelerates Reanimation from Sevoflurane Anesthesia in Mice

WHAT WE ALREADY KNOW ABOUT THIS TOPIC WHAT THIS ARTICLE TELLS US THAT IS NEW BACKGROUND:The parabrachial nucleus (PBN), which is a brainstem region containing glutamatergic neurons, is a key arousal nucleus. Injuries to the area often prevent patient reanimation. Some studies suggest that brain regi...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Anesthesiology (Philadelphia) 2019-01, Vol.130 (1), p.106-118
Hauptverfasser: Wang, Tian-Xiao, Xiong, Bo, Xu, Wei, Wei, Hao-Hua, Qu, Wei-Min, Hong, Zong-Yuan, Huang, Zhi-Li
Format: Artikel
Sprache:eng
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 118
container_issue 1
container_start_page 106
container_title Anesthesiology (Philadelphia)
container_volume 130
creator Wang, Tian-Xiao
Xiong, Bo
Xu, Wei
Wei, Hao-Hua
Qu, Wei-Min
Hong, Zong-Yuan
Huang, Zhi-Li
description WHAT WE ALREADY KNOW ABOUT THIS TOPIC WHAT THIS ARTICLE TELLS US THAT IS NEW BACKGROUND:The parabrachial nucleus (PBN), which is a brainstem region containing glutamatergic neurons, is a key arousal nucleus. Injuries to the area often prevent patient reanimation. Some studies suggest that brain regions that control arousal and reanimation are a key part of the anesthesia recovery. Therefore, we hypothesize that the PBN may be involved in regulating emergence from anesthesia. METHODS:We investigated the effects of specific activation or inhibition of PBN glutamatergic neurons on sevoflurane general anesthesia using the chemogenetic “designer receptors exclusively activated by designer drugs” approach. Optogenetic methods combined with polysomnographic recordings were used to explore the effects of transient activation of PBN glutamatergic neuron on sevoflurane anesthesia. Immunohistochemical techniques are employed to reveal the mechanism by which PBN regulated sevoflurane anesthesia. RESULTS:Chemogenetic activation of PBN glutamatergic neurons by intraperitoneal injections of clozapine-N-oxide decreased emergence time (mean ± SD, control vs. clozapine-N-oxide, 55 ± 24 vs. 15 ± 9 s, P = 0.0002) caused by sevoflurane inhalation and prolonged induction time (70 ± 15 vs. 109 ± 38 s, n = 9, P = 0.012) as well as the ED50 of sevoflurane (1.48 vs. 1.60%, P = 0.0002), which was characterized by a rightward shift of the loss of righting reflex cumulative curve. In contrast, chemogenetic inhibition of PBN glutamatergic neurons slightly increased emergence time (56 ± 26 vs. 87 ± 26 s, n = 8, P = 0.034). Moreover, instantaneous activation of PBN glutamatergic neurons expressing channelrhodopsin-2 during steady-state general anesthesia with sevoflurane produced electroencephalogram evidence of cortical arousal. Immunohistochemical experiments showed that activation of PBN induced excitation of cortical and subcortical arousal nuclei during sevoflurane anesthesia. CONCLUSIONS:Activation of PBN glutamatergic neurons is helpful to accelerate the transition from general anesthesia to an arousal state, which may provide a new strategy in shortening the recovery time after sevoflurane anesthesia.
doi_str_mv 10.1097/ALN.0000000000002475
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2121495539</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2121495539</sourcerecordid><originalsourceid>FETCH-LOGICAL-c5645-1be86d1af9d45a0778bbf70f9ac5a0965d61b3c91b22bdd1dad6c77c788dc6123</originalsourceid><addsrcrecordid>eNqFUE1P3DAUtCpQWSj_oKp85BLqzzg5RqhQpO2C2nKOHPul69aJqR2D-u9rurSqOMC7PM3TzHg8CL2l5JSSVr3v1ptT8t8woeQrtKKSNRWlSu6hVbnyihPGDtBhSt8LVJI3r9EBJ5xJJcQKLZ1Z3J1eXJhxGPG1jnqI2myd9niTjYec8IXPi570AvGbM3gDOYY54c4Y8BDLOeHPoGc37VzGGCb8Be7C6HPUM-BuhrRsITmN3Yw_OQNv0P6ofYLjx32Ebs4_fD37WK2vLi7PunVlZC1kRQdoakv12FohNVGqGYZRkbHVpsC2lramAzctHRgbrKVW29ooZVTTWFNTxo_Qyc73NoafuaToJ5dKal9ihZx6RhkVrZS8LVSxo5oYUoow9rex_Cj-6inpH_ruS9_9076L7N3jC3mYwP4T_S24EJod4T74UmD64fM9xH4L2i_bl7zFM9I_PClYxQhtCS2gehBy_hvfB53A</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2121495539</pqid></control><display><type>article</type><title>Activation of Parabrachial Nucleus Glutamatergic Neurons Accelerates Reanimation from Sevoflurane Anesthesia in Mice</title><source>Journals@Ovid Ovid Autoload</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><creator>Wang, Tian-Xiao ; Xiong, Bo ; Xu, Wei ; Wei, Hao-Hua ; Qu, Wei-Min ; Hong, Zong-Yuan ; Huang, Zhi-Li</creator><creatorcontrib>Wang, Tian-Xiao ; Xiong, Bo ; Xu, Wei ; Wei, Hao-Hua ; Qu, Wei-Min ; Hong, Zong-Yuan ; Huang, Zhi-Li</creatorcontrib><description>WHAT WE ALREADY KNOW ABOUT THIS TOPIC WHAT THIS ARTICLE TELLS US THAT IS NEW BACKGROUND:The parabrachial nucleus (PBN), which is a brainstem region containing glutamatergic neurons, is a key arousal nucleus. Injuries to the area often prevent patient reanimation. Some studies suggest that brain regions that control arousal and reanimation are a key part of the anesthesia recovery. Therefore, we hypothesize that the PBN may be involved in regulating emergence from anesthesia. METHODS:We investigated the effects of specific activation or inhibition of PBN glutamatergic neurons on sevoflurane general anesthesia using the chemogenetic “designer receptors exclusively activated by designer drugs” approach. Optogenetic methods combined with polysomnographic recordings were used to explore the effects of transient activation of PBN glutamatergic neuron on sevoflurane anesthesia. Immunohistochemical techniques are employed to reveal the mechanism by which PBN regulated sevoflurane anesthesia. RESULTS:Chemogenetic activation of PBN glutamatergic neurons by intraperitoneal injections of clozapine-N-oxide decreased emergence time (mean ± SD, control vs. clozapine-N-oxide, 55 ± 24 vs. 15 ± 9 s, P = 0.0002) caused by sevoflurane inhalation and prolonged induction time (70 ± 15 vs. 109 ± 38 s, n = 9, P = 0.012) as well as the ED50 of sevoflurane (1.48 vs. 1.60%, P = 0.0002), which was characterized by a rightward shift of the loss of righting reflex cumulative curve. In contrast, chemogenetic inhibition of PBN glutamatergic neurons slightly increased emergence time (56 ± 26 vs. 87 ± 26 s, n = 8, P = 0.034). Moreover, instantaneous activation of PBN glutamatergic neurons expressing channelrhodopsin-2 during steady-state general anesthesia with sevoflurane produced electroencephalogram evidence of cortical arousal. Immunohistochemical experiments showed that activation of PBN induced excitation of cortical and subcortical arousal nuclei during sevoflurane anesthesia. CONCLUSIONS:Activation of PBN glutamatergic neurons is helpful to accelerate the transition from general anesthesia to an arousal state, which may provide a new strategy in shortening the recovery time after sevoflurane anesthesia.</description><identifier>ISSN: 0003-3022</identifier><identifier>EISSN: 1528-1175</identifier><identifier>DOI: 10.1097/ALN.0000000000002475</identifier><identifier>PMID: 30325744</identifier><language>eng</language><publisher>United States: the American Society of Anesthesiologists, Inc. Wolters Kluwer Health, Inc</publisher><ispartof>Anesthesiology (Philadelphia), 2019-01, Vol.130 (1), p.106-118</ispartof><rights>the American Society of Anesthesiologists, Inc. Wolters Kluwer Health, Inc. All Rights Reserved.</rights><rights>Copyright © by 2019, the American Society of Anesthesiologists, Inc. Wolters Kluwer Health, Inc. All Rights Reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5645-1be86d1af9d45a0778bbf70f9ac5a0965d61b3c91b22bdd1dad6c77c788dc6123</citedby><cites>FETCH-LOGICAL-c5645-1be86d1af9d45a0778bbf70f9ac5a0965d61b3c91b22bdd1dad6c77c788dc6123</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30325744$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wang, Tian-Xiao</creatorcontrib><creatorcontrib>Xiong, Bo</creatorcontrib><creatorcontrib>Xu, Wei</creatorcontrib><creatorcontrib>Wei, Hao-Hua</creatorcontrib><creatorcontrib>Qu, Wei-Min</creatorcontrib><creatorcontrib>Hong, Zong-Yuan</creatorcontrib><creatorcontrib>Huang, Zhi-Li</creatorcontrib><title>Activation of Parabrachial Nucleus Glutamatergic Neurons Accelerates Reanimation from Sevoflurane Anesthesia in Mice</title><title>Anesthesiology (Philadelphia)</title><addtitle>Anesthesiology</addtitle><description>WHAT WE ALREADY KNOW ABOUT THIS TOPIC WHAT THIS ARTICLE TELLS US THAT IS NEW BACKGROUND:The parabrachial nucleus (PBN), which is a brainstem region containing glutamatergic neurons, is a key arousal nucleus. Injuries to the area often prevent patient reanimation. Some studies suggest that brain regions that control arousal and reanimation are a key part of the anesthesia recovery. Therefore, we hypothesize that the PBN may be involved in regulating emergence from anesthesia. METHODS:We investigated the effects of specific activation or inhibition of PBN glutamatergic neurons on sevoflurane general anesthesia using the chemogenetic “designer receptors exclusively activated by designer drugs” approach. Optogenetic methods combined with polysomnographic recordings were used to explore the effects of transient activation of PBN glutamatergic neuron on sevoflurane anesthesia. Immunohistochemical techniques are employed to reveal the mechanism by which PBN regulated sevoflurane anesthesia. RESULTS:Chemogenetic activation of PBN glutamatergic neurons by intraperitoneal injections of clozapine-N-oxide decreased emergence time (mean ± SD, control vs. clozapine-N-oxide, 55 ± 24 vs. 15 ± 9 s, P = 0.0002) caused by sevoflurane inhalation and prolonged induction time (70 ± 15 vs. 109 ± 38 s, n = 9, P = 0.012) as well as the ED50 of sevoflurane (1.48 vs. 1.60%, P = 0.0002), which was characterized by a rightward shift of the loss of righting reflex cumulative curve. In contrast, chemogenetic inhibition of PBN glutamatergic neurons slightly increased emergence time (56 ± 26 vs. 87 ± 26 s, n = 8, P = 0.034). Moreover, instantaneous activation of PBN glutamatergic neurons expressing channelrhodopsin-2 during steady-state general anesthesia with sevoflurane produced electroencephalogram evidence of cortical arousal. Immunohistochemical experiments showed that activation of PBN induced excitation of cortical and subcortical arousal nuclei during sevoflurane anesthesia. CONCLUSIONS:Activation of PBN glutamatergic neurons is helpful to accelerate the transition from general anesthesia to an arousal state, which may provide a new strategy in shortening the recovery time after sevoflurane anesthesia.</description><issn>0003-3022</issn><issn>1528-1175</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><recordid>eNqFUE1P3DAUtCpQWSj_oKp85BLqzzg5RqhQpO2C2nKOHPul69aJqR2D-u9rurSqOMC7PM3TzHg8CL2l5JSSVr3v1ptT8t8woeQrtKKSNRWlSu6hVbnyihPGDtBhSt8LVJI3r9EBJ5xJJcQKLZ1Z3J1eXJhxGPG1jnqI2myd9niTjYec8IXPi570AvGbM3gDOYY54c4Y8BDLOeHPoGc37VzGGCb8Be7C6HPUM-BuhrRsITmN3Yw_OQNv0P6ofYLjx32Ebs4_fD37WK2vLi7PunVlZC1kRQdoakv12FohNVGqGYZRkbHVpsC2lramAzctHRgbrKVW29ooZVTTWFNTxo_Qyc73NoafuaToJ5dKal9ihZx6RhkVrZS8LVSxo5oYUoow9rex_Cj-6inpH_ruS9_9076L7N3jC3mYwP4T_S24EJod4T74UmD64fM9xH4L2i_bl7zFM9I_PClYxQhtCS2gehBy_hvfB53A</recordid><startdate>20190101</startdate><enddate>20190101</enddate><creator>Wang, Tian-Xiao</creator><creator>Xiong, Bo</creator><creator>Xu, Wei</creator><creator>Wei, Hao-Hua</creator><creator>Qu, Wei-Min</creator><creator>Hong, Zong-Yuan</creator><creator>Huang, Zhi-Li</creator><general>the American Society of Anesthesiologists, Inc. Wolters Kluwer Health, Inc</general><general>Copyright by , the American Society of Anesthesiologists, Inc. Wolters Kluwer Health, Inc</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20190101</creationdate><title>Activation of Parabrachial Nucleus Glutamatergic Neurons Accelerates Reanimation from Sevoflurane Anesthesia in Mice</title><author>Wang, Tian-Xiao ; Xiong, Bo ; Xu, Wei ; Wei, Hao-Hua ; Qu, Wei-Min ; Hong, Zong-Yuan ; Huang, Zhi-Li</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5645-1be86d1af9d45a0778bbf70f9ac5a0965d61b3c91b22bdd1dad6c77c788dc6123</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wang, Tian-Xiao</creatorcontrib><creatorcontrib>Xiong, Bo</creatorcontrib><creatorcontrib>Xu, Wei</creatorcontrib><creatorcontrib>Wei, Hao-Hua</creatorcontrib><creatorcontrib>Qu, Wei-Min</creatorcontrib><creatorcontrib>Hong, Zong-Yuan</creatorcontrib><creatorcontrib>Huang, Zhi-Li</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Anesthesiology (Philadelphia)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wang, Tian-Xiao</au><au>Xiong, Bo</au><au>Xu, Wei</au><au>Wei, Hao-Hua</au><au>Qu, Wei-Min</au><au>Hong, Zong-Yuan</au><au>Huang, Zhi-Li</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Activation of Parabrachial Nucleus Glutamatergic Neurons Accelerates Reanimation from Sevoflurane Anesthesia in Mice</atitle><jtitle>Anesthesiology (Philadelphia)</jtitle><addtitle>Anesthesiology</addtitle><date>2019-01-01</date><risdate>2019</risdate><volume>130</volume><issue>1</issue><spage>106</spage><epage>118</epage><pages>106-118</pages><issn>0003-3022</issn><eissn>1528-1175</eissn><abstract>WHAT WE ALREADY KNOW ABOUT THIS TOPIC WHAT THIS ARTICLE TELLS US THAT IS NEW BACKGROUND:The parabrachial nucleus (PBN), which is a brainstem region containing glutamatergic neurons, is a key arousal nucleus. Injuries to the area often prevent patient reanimation. Some studies suggest that brain regions that control arousal and reanimation are a key part of the anesthesia recovery. Therefore, we hypothesize that the PBN may be involved in regulating emergence from anesthesia. METHODS:We investigated the effects of specific activation or inhibition of PBN glutamatergic neurons on sevoflurane general anesthesia using the chemogenetic “designer receptors exclusively activated by designer drugs” approach. Optogenetic methods combined with polysomnographic recordings were used to explore the effects of transient activation of PBN glutamatergic neuron on sevoflurane anesthesia. Immunohistochemical techniques are employed to reveal the mechanism by which PBN regulated sevoflurane anesthesia. RESULTS:Chemogenetic activation of PBN glutamatergic neurons by intraperitoneal injections of clozapine-N-oxide decreased emergence time (mean ± SD, control vs. clozapine-N-oxide, 55 ± 24 vs. 15 ± 9 s, P = 0.0002) caused by sevoflurane inhalation and prolonged induction time (70 ± 15 vs. 109 ± 38 s, n = 9, P = 0.012) as well as the ED50 of sevoflurane (1.48 vs. 1.60%, P = 0.0002), which was characterized by a rightward shift of the loss of righting reflex cumulative curve. In contrast, chemogenetic inhibition of PBN glutamatergic neurons slightly increased emergence time (56 ± 26 vs. 87 ± 26 s, n = 8, P = 0.034). Moreover, instantaneous activation of PBN glutamatergic neurons expressing channelrhodopsin-2 during steady-state general anesthesia with sevoflurane produced electroencephalogram evidence of cortical arousal. Immunohistochemical experiments showed that activation of PBN induced excitation of cortical and subcortical arousal nuclei during sevoflurane anesthesia. CONCLUSIONS:Activation of PBN glutamatergic neurons is helpful to accelerate the transition from general anesthesia to an arousal state, which may provide a new strategy in shortening the recovery time after sevoflurane anesthesia.</abstract><cop>United States</cop><pub>the American Society of Anesthesiologists, Inc. Wolters Kluwer Health, Inc</pub><pmid>30325744</pmid><doi>10.1097/ALN.0000000000002475</doi><tpages>13</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0003-3022
ispartof Anesthesiology (Philadelphia), 2019-01, Vol.130 (1), p.106-118
issn 0003-3022
1528-1175
language eng
recordid cdi_proquest_miscellaneous_2121495539
source Journals@Ovid Ovid Autoload; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals
title Activation of Parabrachial Nucleus Glutamatergic Neurons Accelerates Reanimation from Sevoflurane Anesthesia in Mice
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-08T08%3A25%3A48IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Activation%20of%20Parabrachial%20Nucleus%20Glutamatergic%20Neurons%20Accelerates%20Reanimation%20from%20Sevoflurane%20Anesthesia%20in%20Mice&rft.jtitle=Anesthesiology%20(Philadelphia)&rft.au=Wang,%20Tian-Xiao&rft.date=2019-01-01&rft.volume=130&rft.issue=1&rft.spage=106&rft.epage=118&rft.pages=106-118&rft.issn=0003-3022&rft.eissn=1528-1175&rft_id=info:doi/10.1097/ALN.0000000000002475&rft_dat=%3Cproquest_cross%3E2121495539%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2121495539&rft_id=info:pmid/30325744&rfr_iscdi=true