Different neural circuitry is involved in physiological and psychological stress-induced PTSD-like “nightmares” in rats
Posttraumatic nightmares are a core component of posttraumatic stress disorder (PTSD) and mechanistically linked to the development and maintenance of this disorder, but little is known about their mechanism. We utilized a communication box to establish an animal model of physiological stress (foot-...
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creator | Yu, Bin Cui, Su-Ying Zhang, Xue-Qiong Cui, Xiang-Yu Li, Sheng-Jie Sheng, Zhao-Fu Cao, Qing Huang, Yuan-Li Xu, Ya-Ping Lin, Zhi-Ge Yang, Guang Song, Jin-Zhi Ding, Hui Zhang, Yong-He |
description | Posttraumatic nightmares are a core component of posttraumatic stress disorder (PTSD) and mechanistically linked to the development and maintenance of this disorder, but little is known about their mechanism. We utilized a communication box to establish an animal model of physiological stress (foot-shock [FS]) and psychological stress (PS) to mimic the direct suffering and witnessing of traumatic events. Twenty-one days after traumatic stress, some of the experimental animals presented startled awakening (i.e., were startled awake by a supposed “nightmare”) with different electroencephalographic spectra features. Our neuroanatomical results showed that the secondary somatosensory cortex and primary auditory cortex may play an important role in remote traumatic memory retrieval in FS “nightmare” (FSN) rats, whereas the temporal association cortex may play an important role in PS “nightmare” (PSN) rats. The FSN and PSN groups possessed common emotion evocation circuits, including activation of the amygdala and inactivation of the infralimbic prefrontal cortex and ventral anterior cingulate cortex. The decreased activity of the granular and dysgranular insular cortex was only observed in PSN rats. The present results imply that different types of stress may cause PTSD-like “nightmares” in rodents and identified the possible neurocircuitry of memory retrieval and emotion evocation. |
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We utilized a communication box to establish an animal model of physiological stress (foot-shock [FS]) and psychological stress (PS) to mimic the direct suffering and witnessing of traumatic events. Twenty-one days after traumatic stress, some of the experimental animals presented startled awakening (i.e., were startled awake by a supposed “nightmare”) with different electroencephalographic spectra features. Our neuroanatomical results showed that the secondary somatosensory cortex and primary auditory cortex may play an important role in remote traumatic memory retrieval in FS “nightmare” (FSN) rats, whereas the temporal association cortex may play an important role in PS “nightmare” (PSN) rats. The FSN and PSN groups possessed common emotion evocation circuits, including activation of the amygdala and inactivation of the infralimbic prefrontal cortex and ventral anterior cingulate cortex. The decreased activity of the granular and dysgranular insular cortex was only observed in PSN rats. The present results imply that different types of stress may cause PTSD-like “nightmares” in rodents and identified the possible neurocircuitry of memory retrieval and emotion evocation.</description><identifier>ISSN: 2045-2322</identifier><identifier>EISSN: 2045-2322</identifier><identifier>DOI: 10.1038/srep15976</identifier><identifier>PMID: 26530305</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>13/51 ; 631/378/3920 ; 692/308/1426 ; Amygdala ; Anatomy ; Animal models ; Animals ; Auditory Cortex - physiology ; Auditory pathways ; Circuits ; Cortex (auditory) ; Cortex (cingulate) ; Cortex (insular) ; Dreams - physiology ; EEG ; Electroencephalography ; Feet ; Female ; Footshock ; Humanities and Social Sciences ; Inactivation ; Memory - physiology ; Models, Animal ; multidisciplinary ; Neural networks ; Physiology ; Post traumatic stress disorder ; Prefrontal cortex ; Proto-Oncogene Proteins c-fos - metabolism ; Rats ; Rats, Sprague-Dawley ; Rodents ; Science ; Sleep - physiology ; Somatosensory cortex ; Somatosensory Cortex - physiology ; Stress Disorders, Post-Traumatic - physiopathology ; Stress, Physiological - physiology ; Stress, Psychological - physiopathology ; Temporal Lobe</subject><ispartof>Scientific reports, 2015-11, Vol.5 (1), p.15976-15976, Article 15976</ispartof><rights>The Author(s) 2015</rights><rights>Copyright Nature Publishing Group Nov 2015</rights><rights>Copyright © 2015, Macmillan Publishers Limited 2015 Macmillan Publishers Limited</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c537t-f19650b688c782e21c77ddc3fe4093e4a433234b555377666c30f4def6090dcd3</citedby><cites>FETCH-LOGICAL-c537t-f19650b688c782e21c77ddc3fe4093e4a433234b555377666c30f4def6090dcd3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4632128/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4632128/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,860,881,27901,27902,41096,42165,51551,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26530305$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Yu, Bin</creatorcontrib><creatorcontrib>Cui, Su-Ying</creatorcontrib><creatorcontrib>Zhang, Xue-Qiong</creatorcontrib><creatorcontrib>Cui, Xiang-Yu</creatorcontrib><creatorcontrib>Li, Sheng-Jie</creatorcontrib><creatorcontrib>Sheng, Zhao-Fu</creatorcontrib><creatorcontrib>Cao, Qing</creatorcontrib><creatorcontrib>Huang, Yuan-Li</creatorcontrib><creatorcontrib>Xu, Ya-Ping</creatorcontrib><creatorcontrib>Lin, Zhi-Ge</creatorcontrib><creatorcontrib>Yang, Guang</creatorcontrib><creatorcontrib>Song, Jin-Zhi</creatorcontrib><creatorcontrib>Ding, Hui</creatorcontrib><creatorcontrib>Zhang, Yong-He</creatorcontrib><title>Different neural circuitry is involved in physiological and psychological stress-induced PTSD-like “nightmares” in rats</title><title>Scientific reports</title><addtitle>Sci Rep</addtitle><addtitle>Sci Rep</addtitle><description>Posttraumatic nightmares are a core component of posttraumatic stress disorder (PTSD) and mechanistically linked to the development and maintenance of this disorder, but little is known about their mechanism. We utilized a communication box to establish an animal model of physiological stress (foot-shock [FS]) and psychological stress (PS) to mimic the direct suffering and witnessing of traumatic events. Twenty-one days after traumatic stress, some of the experimental animals presented startled awakening (i.e., were startled awake by a supposed “nightmare”) with different electroencephalographic spectra features. Our neuroanatomical results showed that the secondary somatosensory cortex and primary auditory cortex may play an important role in remote traumatic memory retrieval in FS “nightmare” (FSN) rats, whereas the temporal association cortex may play an important role in PS “nightmare” (PSN) rats. The FSN and PSN groups possessed common emotion evocation circuits, including activation of the amygdala and inactivation of the infralimbic prefrontal cortex and ventral anterior cingulate cortex. The decreased activity of the granular and dysgranular insular cortex was only observed in PSN rats. The present results imply that different types of stress may cause PTSD-like “nightmares” in rodents and identified the possible neurocircuitry of memory retrieval and emotion evocation.</description><subject>13/51</subject><subject>631/378/3920</subject><subject>692/308/1426</subject><subject>Amygdala</subject><subject>Anatomy</subject><subject>Animal models</subject><subject>Animals</subject><subject>Auditory Cortex - physiology</subject><subject>Auditory pathways</subject><subject>Circuits</subject><subject>Cortex (auditory)</subject><subject>Cortex (cingulate)</subject><subject>Cortex (insular)</subject><subject>Dreams - physiology</subject><subject>EEG</subject><subject>Electroencephalography</subject><subject>Feet</subject><subject>Female</subject><subject>Footshock</subject><subject>Humanities and Social Sciences</subject><subject>Inactivation</subject><subject>Memory - physiology</subject><subject>Models, Animal</subject><subject>multidisciplinary</subject><subject>Neural networks</subject><subject>Physiology</subject><subject>Post traumatic stress disorder</subject><subject>Prefrontal cortex</subject><subject>Proto-Oncogene Proteins c-fos - metabolism</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Rodents</subject><subject>Science</subject><subject>Sleep - physiology</subject><subject>Somatosensory cortex</subject><subject>Somatosensory Cortex - physiology</subject><subject>Stress Disorders, Post-Traumatic - physiopathology</subject><subject>Stress, Physiological - physiology</subject><subject>Stress, Psychological - physiopathology</subject><subject>Temporal Lobe</subject><issn>2045-2322</issn><issn>2045-2322</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>C6C</sourceid><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNplkd9qFDEUxoMotmx74QvIgDdamJr_mdwI0moVCgrW6zCbZHZTZ5MxmVlYvOmD1Jfrk_SUrcuquckh55cv38mH0AuCTwlmzduS_UCEVvIJOqSYi5oySp_u1QfouJRrDEtQzYl-jg6oFAwzLA7Rr_PQdT77OFbRT7ntKxuyncKYN1UoVYjr1K-9g6IalpsSUp8WwQLWRlcNZWOXu5MyZl9KHaKbLNz4evXtvO7DD1_d3dzGsFiOqxaAu5vfD2K5HcsReta1ffHHj_sMff_44ersU3355eLz2fvL2gqmxrojWgo8l01jVUM9JVYp5yzrPMeaed5yxijjcyEAV1JKy3DHne8k1thZx2bo3VZ3mOYr7ywMC4OaIQdwtDGpDebvTgxLs0hrwyWjhDYg8PpRIKefky-jWYVifd-30aepGKIYlg0W8Ksz9Oof9DpNOcJ4hjRaK60E5UC92VI2pwIBdjszBJuHVM0uVWBf7rvfkX8yBOBkCxRoxYXPe0_-p3YPo8qvuA</recordid><startdate>20151104</startdate><enddate>20151104</enddate><creator>Yu, Bin</creator><creator>Cui, Su-Ying</creator><creator>Zhang, Xue-Qiong</creator><creator>Cui, Xiang-Yu</creator><creator>Li, Sheng-Jie</creator><creator>Sheng, Zhao-Fu</creator><creator>Cao, Qing</creator><creator>Huang, Yuan-Li</creator><creator>Xu, Ya-Ping</creator><creator>Lin, Zhi-Ge</creator><creator>Yang, Guang</creator><creator>Song, Jin-Zhi</creator><creator>Ding, Hui</creator><creator>Zhang, Yong-He</creator><general>Nature Publishing Group UK</general><general>Nature Publishing Group</general><scope>C6C</scope><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>88A</scope><scope>88E</scope><scope>88I</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M7P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20151104</creationdate><title>Different neural circuitry is involved in physiological and psychological stress-induced PTSD-like “nightmares” in rats</title><author>Yu, Bin ; Cui, Su-Ying ; Zhang, Xue-Qiong ; Cui, Xiang-Yu ; Li, Sheng-Jie ; Sheng, Zhao-Fu ; Cao, Qing ; Huang, Yuan-Li ; Xu, Ya-Ping ; Lin, Zhi-Ge ; Yang, Guang ; Song, Jin-Zhi ; Ding, Hui ; Zhang, Yong-He</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c537t-f19650b688c782e21c77ddc3fe4093e4a433234b555377666c30f4def6090dcd3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>13/51</topic><topic>631/378/3920</topic><topic>692/308/1426</topic><topic>Amygdala</topic><topic>Anatomy</topic><topic>Animal models</topic><topic>Animals</topic><topic>Auditory Cortex - physiology</topic><topic>Auditory pathways</topic><topic>Circuits</topic><topic>Cortex (auditory)</topic><topic>Cortex (cingulate)</topic><topic>Cortex (insular)</topic><topic>Dreams - physiology</topic><topic>EEG</topic><topic>Electroencephalography</topic><topic>Feet</topic><topic>Female</topic><topic>Footshock</topic><topic>Humanities and Social Sciences</topic><topic>Inactivation</topic><topic>Memory - physiology</topic><topic>Models, Animal</topic><topic>multidisciplinary</topic><topic>Neural networks</topic><topic>Physiology</topic><topic>Post traumatic stress disorder</topic><topic>Prefrontal cortex</topic><topic>Proto-Oncogene Proteins c-fos - metabolism</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Rodents</topic><topic>Science</topic><topic>Sleep - physiology</topic><topic>Somatosensory cortex</topic><topic>Somatosensory Cortex - physiology</topic><topic>Stress Disorders, Post-Traumatic - physiopathology</topic><topic>Stress, Physiological - physiology</topic><topic>Stress, Psychological - physiopathology</topic><topic>Temporal Lobe</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yu, Bin</creatorcontrib><creatorcontrib>Cui, Su-Ying</creatorcontrib><creatorcontrib>Zhang, Xue-Qiong</creatorcontrib><creatorcontrib>Cui, Xiang-Yu</creatorcontrib><creatorcontrib>Li, Sheng-Jie</creatorcontrib><creatorcontrib>Sheng, Zhao-Fu</creatorcontrib><creatorcontrib>Cao, Qing</creatorcontrib><creatorcontrib>Huang, Yuan-Li</creatorcontrib><creatorcontrib>Xu, Ya-Ping</creatorcontrib><creatorcontrib>Lin, Zhi-Ge</creatorcontrib><creatorcontrib>Yang, Guang</creatorcontrib><creatorcontrib>Song, Jin-Zhi</creatorcontrib><creatorcontrib>Ding, Hui</creatorcontrib><creatorcontrib>Zhang, Yong-He</creatorcontrib><collection>Springer Nature OA Free Journals</collection><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>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</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>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Science Database</collection><collection>Biological Science Database</collection><collection>Publicly Available Content Database</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 Basic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Scientific reports</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yu, Bin</au><au>Cui, Su-Ying</au><au>Zhang, Xue-Qiong</au><au>Cui, Xiang-Yu</au><au>Li, Sheng-Jie</au><au>Sheng, Zhao-Fu</au><au>Cao, Qing</au><au>Huang, Yuan-Li</au><au>Xu, Ya-Ping</au><au>Lin, Zhi-Ge</au><au>Yang, Guang</au><au>Song, Jin-Zhi</au><au>Ding, Hui</au><au>Zhang, Yong-He</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Different neural circuitry is involved in physiological and psychological stress-induced PTSD-like “nightmares” in rats</atitle><jtitle>Scientific reports</jtitle><stitle>Sci Rep</stitle><addtitle>Sci Rep</addtitle><date>2015-11-04</date><risdate>2015</risdate><volume>5</volume><issue>1</issue><spage>15976</spage><epage>15976</epage><pages>15976-15976</pages><artnum>15976</artnum><issn>2045-2322</issn><eissn>2045-2322</eissn><abstract>Posttraumatic nightmares are a core component of posttraumatic stress disorder (PTSD) and mechanistically linked to the development and maintenance of this disorder, but little is known about their mechanism. We utilized a communication box to establish an animal model of physiological stress (foot-shock [FS]) and psychological stress (PS) to mimic the direct suffering and witnessing of traumatic events. Twenty-one days after traumatic stress, some of the experimental animals presented startled awakening (i.e., were startled awake by a supposed “nightmare”) with different electroencephalographic spectra features. Our neuroanatomical results showed that the secondary somatosensory cortex and primary auditory cortex may play an important role in remote traumatic memory retrieval in FS “nightmare” (FSN) rats, whereas the temporal association cortex may play an important role in PS “nightmare” (PSN) rats. The FSN and PSN groups possessed common emotion evocation circuits, including activation of the amygdala and inactivation of the infralimbic prefrontal cortex and ventral anterior cingulate cortex. The decreased activity of the granular and dysgranular insular cortex was only observed in PSN rats. The present results imply that different types of stress may cause PTSD-like “nightmares” in rodents and identified the possible neurocircuitry of memory retrieval and emotion evocation.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>26530305</pmid><doi>10.1038/srep15976</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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subjects | 13/51 631/378/3920 692/308/1426 Amygdala Anatomy Animal models Animals Auditory Cortex - physiology Auditory pathways Circuits Cortex (auditory) Cortex (cingulate) Cortex (insular) Dreams - physiology EEG Electroencephalography Feet Female Footshock Humanities and Social Sciences Inactivation Memory - physiology Models, Animal multidisciplinary Neural networks Physiology Post traumatic stress disorder Prefrontal cortex Proto-Oncogene Proteins c-fos - metabolism Rats Rats, Sprague-Dawley Rodents Science Sleep - physiology Somatosensory cortex Somatosensory Cortex - physiology Stress Disorders, Post-Traumatic - physiopathology Stress, Physiological - physiology Stress, Psychological - physiopathology Temporal Lobe |
title | Different neural circuitry is involved in physiological and psychological stress-induced PTSD-like “nightmares” in rats |
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