Thalamic Stimulation Improves Postictal Cortical Arousal and Behavior
The postictal state following seizures is characterized by impaired consciousness and has a major negative impact on individuals with epilepsy. Previous work in disorders of consciousness including the postictal state suggests that bilateral deep brain stimulation (DBS) of the thalamic intralaminar...
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creator | Xu, Jingwen Galardi, Maria Milagros Pok, Brian Patel, Kishan K Zhao, Charlie W Andrews, John P Singla, Shobhit McCafferty, Cian P Feng, Li Musonza, Eric T Kundishora, Adam J Gummadavelli, Abhijeet Gerrard, Jason L Laubach, Mark Schiff, Nicholas D Blumenfeld, Hal |
description | The postictal state following seizures is characterized by impaired consciousness and has a major negative impact on individuals with epilepsy. Previous work in disorders of consciousness including the postictal state suggests that bilateral deep brain stimulation (DBS) of the thalamic intralaminar central lateral nucleus (CL) may improve level of arousal. We tested the effects of postictal thalamic CL DBS in a rat model of secondarily generalized seizures elicited by electrical hippocampal stimulation. Thalamic CL DBS was delivered at 100 Hz during the postictal period in 21 female rats while measuring cortical electrophysiology and behavior. The postictal period was characterized by frontal cortical slow waves, like other states of depressed consciousness. In addition, rats exhibited severely impaired responses on two different behavioral tasks in the postictal state. Thalamic CL stimulation prevented postictal cortical slow wave activity but produced only modest behavioral improvement on a spontaneous licking sucrose reward task. We therefore also tested responses using a lever-press shock escape/avoidance (E/A) task. Rats achieved high success rates responding to the sound warning on the E/A task even during natural slow wave sleep but were severely impaired in the postictal state. Unlike the spontaneous licking task, thalamic CL DBS during the E/A task produced a marked improvement in behavior, with significant increases in lever-press shock avoidance with DBS compared with sham controls. These findings support the idea that DBS of subcortical arousal structures may be a novel therapeutic strategy benefitting patients with medically and surgically refractory epilepsy.
The postictal state following seizures is characterized by impaired consciousness and has a major negative impact on individuals with epilepsy. For the first time, we developed two behavioral tasks and demonstrate that bilateral deep brain stimulation (DBS) of the thalamic intralaminar central lateral nucleus (CL) decreased cortical slow wave activity and improved task performance in the postictal period. Because preclinical task performance studies are crucial to explore the effectiveness and safety of DBS treatment, our work is clinically relevant as it could support and help set the foundations for a human neurostimulation trial to improve postictal responsiveness in patients with medically and surgically refractory epilepsy. |
doi_str_mv | 10.1523/JNEUROSCI.1370-20.2020 |
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The postictal state following seizures is characterized by impaired consciousness and has a major negative impact on individuals with epilepsy. For the first time, we developed two behavioral tasks and demonstrate that bilateral deep brain stimulation (DBS) of the thalamic intralaminar central lateral nucleus (CL) decreased cortical slow wave activity and improved task performance in the postictal period. Because preclinical task performance studies are crucial to explore the effectiveness and safety of DBS treatment, our work is clinically relevant as it could support and help set the foundations for a human neurostimulation trial to improve postictal responsiveness in patients with medically and surgically refractory epilepsy.</description><identifier>ISSN: 0270-6474</identifier><identifier>EISSN: 1529-2401</identifier><identifier>DOI: 10.1523/JNEUROSCI.1370-20.2020</identifier><identifier>PMID: 32826310</identifier><language>eng</language><publisher>United States: Society for Neuroscience</publisher><subject>Animals ; Arousal ; Avoidance ; Avoidance Learning ; Behavior ; Cerebral Cortex - physiopathology ; Consciousness ; Convulsions & seizures ; Deep brain stimulation ; Deep Brain Stimulation - methods ; Electrophysiology ; Epilepsy ; Female ; Hippocampus ; Rats ; Rats, Sprague-Dawley ; Reinforcement ; Reward ; Rodents ; Seizures ; Seizures - physiopathology ; Seizures - therapy ; Sleep ; Stimulation ; Sucrose ; Sugar ; Thalamus ; Thalamus - physiology</subject><ispartof>The Journal of neuroscience, 2020-09, Vol.40 (38), p.7343-7354</ispartof><rights>Copyright © 2020 the authors.</rights><rights>Copyright Society for Neuroscience Sep 16, 2020</rights><rights>Copyright © 2020 the authors 2020</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c442t-555379dd98b6562c1ff50450cff59d4a076b9a98bde5d45117fbd6dd7c057e433</citedby><orcidid>0000-0001-6971-1407 ; 0000-0002-2403-4497</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7534908/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7534908/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,723,776,780,881,27903,27904,53770,53772</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32826310$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Xu, Jingwen</creatorcontrib><creatorcontrib>Galardi, Maria Milagros</creatorcontrib><creatorcontrib>Pok, Brian</creatorcontrib><creatorcontrib>Patel, Kishan K</creatorcontrib><creatorcontrib>Zhao, Charlie W</creatorcontrib><creatorcontrib>Andrews, John P</creatorcontrib><creatorcontrib>Singla, Shobhit</creatorcontrib><creatorcontrib>McCafferty, Cian P</creatorcontrib><creatorcontrib>Feng, Li</creatorcontrib><creatorcontrib>Musonza, Eric T</creatorcontrib><creatorcontrib>Kundishora, Adam J</creatorcontrib><creatorcontrib>Gummadavelli, Abhijeet</creatorcontrib><creatorcontrib>Gerrard, Jason L</creatorcontrib><creatorcontrib>Laubach, Mark</creatorcontrib><creatorcontrib>Schiff, Nicholas D</creatorcontrib><creatorcontrib>Blumenfeld, Hal</creatorcontrib><title>Thalamic Stimulation Improves Postictal Cortical Arousal and Behavior</title><title>The Journal of neuroscience</title><addtitle>J Neurosci</addtitle><description>The postictal state following seizures is characterized by impaired consciousness and has a major negative impact on individuals with epilepsy. Previous work in disorders of consciousness including the postictal state suggests that bilateral deep brain stimulation (DBS) of the thalamic intralaminar central lateral nucleus (CL) may improve level of arousal. We tested the effects of postictal thalamic CL DBS in a rat model of secondarily generalized seizures elicited by electrical hippocampal stimulation. Thalamic CL DBS was delivered at 100 Hz during the postictal period in 21 female rats while measuring cortical electrophysiology and behavior. The postictal period was characterized by frontal cortical slow waves, like other states of depressed consciousness. In addition, rats exhibited severely impaired responses on two different behavioral tasks in the postictal state. Thalamic CL stimulation prevented postictal cortical slow wave activity but produced only modest behavioral improvement on a spontaneous licking sucrose reward task. We therefore also tested responses using a lever-press shock escape/avoidance (E/A) task. Rats achieved high success rates responding to the sound warning on the E/A task even during natural slow wave sleep but were severely impaired in the postictal state. Unlike the spontaneous licking task, thalamic CL DBS during the E/A task produced a marked improvement in behavior, with significant increases in lever-press shock avoidance with DBS compared with sham controls. These findings support the idea that DBS of subcortical arousal structures may be a novel therapeutic strategy benefitting patients with medically and surgically refractory epilepsy.
The postictal state following seizures is characterized by impaired consciousness and has a major negative impact on individuals with epilepsy. For the first time, we developed two behavioral tasks and demonstrate that bilateral deep brain stimulation (DBS) of the thalamic intralaminar central lateral nucleus (CL) decreased cortical slow wave activity and improved task performance in the postictal period. Because preclinical task performance studies are crucial to explore the effectiveness and safety of DBS treatment, our work is clinically relevant as it could support and help set the foundations for a human neurostimulation trial to improve postictal responsiveness in patients with medically and surgically refractory epilepsy.</description><subject>Animals</subject><subject>Arousal</subject><subject>Avoidance</subject><subject>Avoidance Learning</subject><subject>Behavior</subject><subject>Cerebral Cortex - physiopathology</subject><subject>Consciousness</subject><subject>Convulsions & seizures</subject><subject>Deep brain stimulation</subject><subject>Deep Brain Stimulation - methods</subject><subject>Electrophysiology</subject><subject>Epilepsy</subject><subject>Female</subject><subject>Hippocampus</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Reinforcement</subject><subject>Reward</subject><subject>Rodents</subject><subject>Seizures</subject><subject>Seizures - physiopathology</subject><subject>Seizures - therapy</subject><subject>Sleep</subject><subject>Stimulation</subject><subject>Sucrose</subject><subject>Sugar</subject><subject>Thalamus</subject><subject>Thalamus - physiology</subject><issn>0270-6474</issn><issn>1529-2401</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpdUV1rGzEQFKWlcdP-hXDQl76cs_r2vQRS46QOoQ6x8yxkSRcr3J1c6c6Qfx-ZOKYJLMzCzA47DEJnGMaYE3p-83f2cL9YTudjTCWUBMYECHxCo8xWJWGAP6MRkEwJJtkJ-pbSEwBIwPIrOqFkQgTFMEKz1UY3uvWmWPa-HRrd-9AV83Ybw86l4i6k3pteN8U0xLzl5TKGIWXUnS1-u43e-RC_oy-1bpL7ccBT9HA1W03_lLeL6_n08rY0jJG-5JxTWVlbTdaCC2JwXXNgHEzGyjINUqwrnVnruGUcY1mvrbBWGuDSMUpP0cWr73ZYt84a1_VRN2obfavjswraq_dM5zfqMeyU5JRVMMkGvw4GMfwbXOpV65NxTaM7l2MpwqigFZO4ytKfH6RPYYhdjpdVTEjCJ3L_kXhVmRhSiq4-PoNB7ZtSx6bUvilF9kMgH579H-V49lYNfQHBzpCC</recordid><startdate>20200916</startdate><enddate>20200916</enddate><creator>Xu, Jingwen</creator><creator>Galardi, Maria Milagros</creator><creator>Pok, Brian</creator><creator>Patel, Kishan K</creator><creator>Zhao, Charlie W</creator><creator>Andrews, John P</creator><creator>Singla, Shobhit</creator><creator>McCafferty, Cian P</creator><creator>Feng, Li</creator><creator>Musonza, Eric T</creator><creator>Kundishora, Adam J</creator><creator>Gummadavelli, Abhijeet</creator><creator>Gerrard, Jason L</creator><creator>Laubach, Mark</creator><creator>Schiff, Nicholas D</creator><creator>Blumenfeld, Hal</creator><general>Society for Neuroscience</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>7QG</scope><scope>7QR</scope><scope>7TK</scope><scope>7U7</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>P64</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0001-6971-1407</orcidid><orcidid>https://orcid.org/0000-0002-2403-4497</orcidid></search><sort><creationdate>20200916</creationdate><title>Thalamic Stimulation Improves Postictal Cortical Arousal and Behavior</title><author>Xu, Jingwen ; Galardi, Maria Milagros ; Pok, Brian ; Patel, Kishan K ; Zhao, Charlie W ; Andrews, John P ; Singla, Shobhit ; McCafferty, Cian P ; Feng, Li ; Musonza, Eric T ; Kundishora, Adam J ; Gummadavelli, Abhijeet ; Gerrard, Jason L ; Laubach, Mark ; Schiff, Nicholas D ; Blumenfeld, Hal</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c442t-555379dd98b6562c1ff50450cff59d4a076b9a98bde5d45117fbd6dd7c057e433</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Animals</topic><topic>Arousal</topic><topic>Avoidance</topic><topic>Avoidance Learning</topic><topic>Behavior</topic><topic>Cerebral Cortex - physiopathology</topic><topic>Consciousness</topic><topic>Convulsions & seizures</topic><topic>Deep brain stimulation</topic><topic>Deep Brain Stimulation - methods</topic><topic>Electrophysiology</topic><topic>Epilepsy</topic><topic>Female</topic><topic>Hippocampus</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Reinforcement</topic><topic>Reward</topic><topic>Rodents</topic><topic>Seizures</topic><topic>Seizures - physiopathology</topic><topic>Seizures - therapy</topic><topic>Sleep</topic><topic>Stimulation</topic><topic>Sucrose</topic><topic>Sugar</topic><topic>Thalamus</topic><topic>Thalamus - physiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Xu, Jingwen</creatorcontrib><creatorcontrib>Galardi, Maria Milagros</creatorcontrib><creatorcontrib>Pok, Brian</creatorcontrib><creatorcontrib>Patel, Kishan K</creatorcontrib><creatorcontrib>Zhao, Charlie W</creatorcontrib><creatorcontrib>Andrews, John P</creatorcontrib><creatorcontrib>Singla, Shobhit</creatorcontrib><creatorcontrib>McCafferty, Cian P</creatorcontrib><creatorcontrib>Feng, Li</creatorcontrib><creatorcontrib>Musonza, Eric T</creatorcontrib><creatorcontrib>Kundishora, Adam J</creatorcontrib><creatorcontrib>Gummadavelli, Abhijeet</creatorcontrib><creatorcontrib>Gerrard, Jason L</creatorcontrib><creatorcontrib>Laubach, Mark</creatorcontrib><creatorcontrib>Schiff, Nicholas D</creatorcontrib><creatorcontrib>Blumenfeld, Hal</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Animal Behavior Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>The Journal of neuroscience</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Xu, Jingwen</au><au>Galardi, Maria Milagros</au><au>Pok, Brian</au><au>Patel, Kishan K</au><au>Zhao, Charlie W</au><au>Andrews, John P</au><au>Singla, Shobhit</au><au>McCafferty, Cian P</au><au>Feng, Li</au><au>Musonza, Eric T</au><au>Kundishora, Adam J</au><au>Gummadavelli, Abhijeet</au><au>Gerrard, Jason L</au><au>Laubach, Mark</au><au>Schiff, Nicholas D</au><au>Blumenfeld, Hal</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Thalamic Stimulation Improves Postictal Cortical Arousal and Behavior</atitle><jtitle>The Journal of neuroscience</jtitle><addtitle>J Neurosci</addtitle><date>2020-09-16</date><risdate>2020</risdate><volume>40</volume><issue>38</issue><spage>7343</spage><epage>7354</epage><pages>7343-7354</pages><issn>0270-6474</issn><eissn>1529-2401</eissn><abstract>The postictal state following seizures is characterized by impaired consciousness and has a major negative impact on individuals with epilepsy. Previous work in disorders of consciousness including the postictal state suggests that bilateral deep brain stimulation (DBS) of the thalamic intralaminar central lateral nucleus (CL) may improve level of arousal. We tested the effects of postictal thalamic CL DBS in a rat model of secondarily generalized seizures elicited by electrical hippocampal stimulation. Thalamic CL DBS was delivered at 100 Hz during the postictal period in 21 female rats while measuring cortical electrophysiology and behavior. The postictal period was characterized by frontal cortical slow waves, like other states of depressed consciousness. In addition, rats exhibited severely impaired responses on two different behavioral tasks in the postictal state. Thalamic CL stimulation prevented postictal cortical slow wave activity but produced only modest behavioral improvement on a spontaneous licking sucrose reward task. We therefore also tested responses using a lever-press shock escape/avoidance (E/A) task. Rats achieved high success rates responding to the sound warning on the E/A task even during natural slow wave sleep but were severely impaired in the postictal state. Unlike the spontaneous licking task, thalamic CL DBS during the E/A task produced a marked improvement in behavior, with significant increases in lever-press shock avoidance with DBS compared with sham controls. These findings support the idea that DBS of subcortical arousal structures may be a novel therapeutic strategy benefitting patients with medically and surgically refractory epilepsy.
The postictal state following seizures is characterized by impaired consciousness and has a major negative impact on individuals with epilepsy. For the first time, we developed two behavioral tasks and demonstrate that bilateral deep brain stimulation (DBS) of the thalamic intralaminar central lateral nucleus (CL) decreased cortical slow wave activity and improved task performance in the postictal period. Because preclinical task performance studies are crucial to explore the effectiveness and safety of DBS treatment, our work is clinically relevant as it could support and help set the foundations for a human neurostimulation trial to improve postictal responsiveness in patients with medically and surgically refractory epilepsy.</abstract><cop>United States</cop><pub>Society for Neuroscience</pub><pmid>32826310</pmid><doi>10.1523/JNEUROSCI.1370-20.2020</doi><tpages>12</tpages><orcidid>https://orcid.org/0000-0001-6971-1407</orcidid><orcidid>https://orcid.org/0000-0002-2403-4497</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Animals Arousal Avoidance Avoidance Learning Behavior Cerebral Cortex - physiopathology Consciousness Convulsions & seizures Deep brain stimulation Deep Brain Stimulation - methods Electrophysiology Epilepsy Female Hippocampus Rats Rats, Sprague-Dawley Reinforcement Reward Rodents Seizures Seizures - physiopathology Seizures - therapy Sleep Stimulation Sucrose Sugar Thalamus Thalamus - physiology |
title | Thalamic Stimulation Improves Postictal Cortical Arousal and Behavior |
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