Cardiac dysregulation following intrahippocampal kainate-induced status epilepticus
Status epilepticus (SE) is a prevalent disorder associated with significant morbidity, including the development of epilepsy and mortality. Cardiac arrhythmias (i.e. inappropriate sinus tachycardia and bradycardia, asystole, and atrioventricular blocks) are observed in patients following SE. We char...
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description | Status epilepticus (SE) is a prevalent disorder associated with significant morbidity, including the development of epilepsy and mortality. Cardiac arrhythmias (i.e. inappropriate sinus tachycardia and bradycardia, asystole, and atrioventricular blocks) are observed in patients following SE. We characterized ictal (during a seizure) and interictal (between seizure) cardiac arrhythmogenesis following SE using continuous electrocardiography and video electroencephalography (vEEG) recordings throughout a 14-day monitoring period in an intrahippocampal chemoconvulsant mouse model that develops epilepsy. We quantified heart rhythm abnormalities and examined whether the frequency of cardiac events correlated with epileptiform activity, circadian (light/dark) cycle, the presence of seizures, and survival during this period of early epileptogenesis (the development of epilepsy) following SE. Shortly following SE, mice developed an increased interictal heart rate and heart rhythm abnormalities (i.e. sinus pause and sinus arrhythmias) when compared to control mice. Heart rhythm abnormalities were more frequent during the light cycle and were not correlated with increased epileptiform activity or seizure frequency. Finally, SE animals had early mortality, and a death event captured during vEEG recording demonstrated severe bradycardia prior to death. These cardiac changes occurred within 14 days after SE and may represent an early risk factor for sudden death following SE. |
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Cardiac arrhythmias (i.e. inappropriate sinus tachycardia and bradycardia, asystole, and atrioventricular blocks) are observed in patients following SE. We characterized ictal (during a seizure) and interictal (between seizure) cardiac arrhythmogenesis following SE using continuous electrocardiography and video electroencephalography (vEEG) recordings throughout a 14-day monitoring period in an intrahippocampal chemoconvulsant mouse model that develops epilepsy. We quantified heart rhythm abnormalities and examined whether the frequency of cardiac events correlated with epileptiform activity, circadian (light/dark) cycle, the presence of seizures, and survival during this period of early epileptogenesis (the development of epilepsy) following SE. Shortly following SE, mice developed an increased interictal heart rate and heart rhythm abnormalities (i.e. sinus pause and sinus arrhythmias) when compared to control mice. Heart rhythm abnormalities were more frequent during the light cycle and were not correlated with increased epileptiform activity or seizure frequency. Finally, SE animals had early mortality, and a death event captured during vEEG recording demonstrated severe bradycardia prior to death. These cardiac changes occurred within 14 days after SE and may represent an early risk factor for sudden death following SE.</description><identifier>ISSN: 2045-2322</identifier><identifier>EISSN: 2045-2322</identifier><identifier>DOI: 10.1038/s41598-020-60324-8</identifier><identifier>PMID: 32132552</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>631/378/1689/178 ; 631/443/376 ; 631/443/592 ; Animals ; Arrhythmias, Cardiac - chemically induced ; Arrhythmias, Cardiac - pathology ; Arrhythmias, Cardiac - physiopathology ; Bradycardia ; Cardiac arrhythmia ; Circadian Rhythm - drug effects ; Circadian rhythms ; Convulsions & seizures ; Death ; Disease Models, Animal ; EEG ; EKG ; Electrocardiography ; Electroencephalography ; Epilepsy ; Heart ; Heart rate ; Humanities and Social Sciences ; Kainic Acid - adverse effects ; Kainic Acid - pharmacology ; Male ; Mice ; Morbidity ; Mortality ; multidisciplinary ; Risk factors ; Science ; Science (multidisciplinary) ; Seizures ; Sinuses ; Status Epilepticus - chemically induced ; Status Epilepticus - physiopathology ; Tachycardia</subject><ispartof>Scientific reports, 2020-03, Vol.10 (1), p.4043, Article 4043</ispartof><rights>The Author(s) 2020</rights><rights>This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c474t-6cb7d2c0b474c6334483de04d11482b2389c53fa76ddf7e38d9360a740c089c53</citedby><cites>FETCH-LOGICAL-c474t-6cb7d2c0b474c6334483de04d11482b2389c53fa76ddf7e38d9360a740c089c53</cites><orcidid>0000-0001-9934-648X ; 0000-0002-1878-9631</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/PMC7055295/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7055295/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,864,885,27924,27925,41120,42189,51576,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32132552$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Levine, Amber T.</creatorcontrib><creatorcontrib>Born, Heather A.</creatorcontrib><creatorcontrib>Landstrom, Andrew P.</creatorcontrib><creatorcontrib>Larson, Samuel</creatorcontrib><creatorcontrib>Lee, Wai Ling</creatorcontrib><creatorcontrib>Dao, An T.</creatorcontrib><creatorcontrib>Wehrens, Xander H.</creatorcontrib><creatorcontrib>Lai, Yi-Chen</creatorcontrib><creatorcontrib>Anderson, Anne E.</creatorcontrib><title>Cardiac dysregulation following intrahippocampal kainate-induced status epilepticus</title><title>Scientific reports</title><addtitle>Sci Rep</addtitle><addtitle>Sci Rep</addtitle><description>Status epilepticus (SE) is a prevalent disorder associated with significant morbidity, including the development of epilepsy and mortality. Cardiac arrhythmias (i.e. inappropriate sinus tachycardia and bradycardia, asystole, and atrioventricular blocks) are observed in patients following SE. We characterized ictal (during a seizure) and interictal (between seizure) cardiac arrhythmogenesis following SE using continuous electrocardiography and video electroencephalography (vEEG) recordings throughout a 14-day monitoring period in an intrahippocampal chemoconvulsant mouse model that develops epilepsy. We quantified heart rhythm abnormalities and examined whether the frequency of cardiac events correlated with epileptiform activity, circadian (light/dark) cycle, the presence of seizures, and survival during this period of early epileptogenesis (the development of epilepsy) following SE. Shortly following SE, mice developed an increased interictal heart rate and heart rhythm abnormalities (i.e. sinus pause and sinus arrhythmias) when compared to control mice. Heart rhythm abnormalities were more frequent during the light cycle and were not correlated with increased epileptiform activity or seizure frequency. Finally, SE animals had early mortality, and a death event captured during vEEG recording demonstrated severe bradycardia prior to death. These cardiac changes occurred within 14 days after SE and may represent an early risk factor for sudden death following SE.</description><subject>631/378/1689/178</subject><subject>631/443/376</subject><subject>631/443/592</subject><subject>Animals</subject><subject>Arrhythmias, Cardiac - chemically induced</subject><subject>Arrhythmias, Cardiac - pathology</subject><subject>Arrhythmias, Cardiac - physiopathology</subject><subject>Bradycardia</subject><subject>Cardiac arrhythmia</subject><subject>Circadian Rhythm - drug effects</subject><subject>Circadian rhythms</subject><subject>Convulsions & seizures</subject><subject>Death</subject><subject>Disease Models, Animal</subject><subject>EEG</subject><subject>EKG</subject><subject>Electrocardiography</subject><subject>Electroencephalography</subject><subject>Epilepsy</subject><subject>Heart</subject><subject>Heart rate</subject><subject>Humanities and Social Sciences</subject><subject>Kainic Acid - adverse effects</subject><subject>Kainic Acid - 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chemically induced</topic><topic>Arrhythmias, Cardiac - pathology</topic><topic>Arrhythmias, Cardiac - physiopathology</topic><topic>Bradycardia</topic><topic>Cardiac arrhythmia</topic><topic>Circadian Rhythm - drug effects</topic><topic>Circadian rhythms</topic><topic>Convulsions & seizures</topic><topic>Death</topic><topic>Disease Models, Animal</topic><topic>EEG</topic><topic>EKG</topic><topic>Electrocardiography</topic><topic>Electroencephalography</topic><topic>Epilepsy</topic><topic>Heart</topic><topic>Heart rate</topic><topic>Humanities and Social Sciences</topic><topic>Kainic Acid - adverse effects</topic><topic>Kainic Acid - pharmacology</topic><topic>Male</topic><topic>Mice</topic><topic>Morbidity</topic><topic>Mortality</topic><topic>multidisciplinary</topic><topic>Risk factors</topic><topic>Science</topic><topic>Science (multidisciplinary)</topic><topic>Seizures</topic><topic>Sinuses</topic><topic>Status Epilepticus - chemically induced</topic><topic>Status Epilepticus - physiopathology</topic><topic>Tachycardia</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Levine, Amber T.</creatorcontrib><creatorcontrib>Born, Heather A.</creatorcontrib><creatorcontrib>Landstrom, Andrew P.</creatorcontrib><creatorcontrib>Larson, Samuel</creatorcontrib><creatorcontrib>Lee, Wai Ling</creatorcontrib><creatorcontrib>Dao, An T.</creatorcontrib><creatorcontrib>Wehrens, Xander H.</creatorcontrib><creatorcontrib>Lai, Yi-Chen</creatorcontrib><creatorcontrib>Anderson, Anne E.</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 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>PubMed Central (Full Participant titles)</collection><jtitle>Scientific reports</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Levine, Amber T.</au><au>Born, Heather A.</au><au>Landstrom, Andrew P.</au><au>Larson, Samuel</au><au>Lee, Wai Ling</au><au>Dao, An T.</au><au>Wehrens, Xander H.</au><au>Lai, Yi-Chen</au><au>Anderson, Anne E.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Cardiac dysregulation following intrahippocampal kainate-induced status epilepticus</atitle><jtitle>Scientific reports</jtitle><stitle>Sci Rep</stitle><addtitle>Sci Rep</addtitle><date>2020-03-04</date><risdate>2020</risdate><volume>10</volume><issue>1</issue><spage>4043</spage><pages>4043-</pages><artnum>4043</artnum><issn>2045-2322</issn><eissn>2045-2322</eissn><abstract>Status epilepticus (SE) is a prevalent disorder associated with significant morbidity, including the development of epilepsy and mortality. Cardiac arrhythmias (i.e. inappropriate sinus tachycardia and bradycardia, asystole, and atrioventricular blocks) are observed in patients following SE. We characterized ictal (during a seizure) and interictal (between seizure) cardiac arrhythmogenesis following SE using continuous electrocardiography and video electroencephalography (vEEG) recordings throughout a 14-day monitoring period in an intrahippocampal chemoconvulsant mouse model that develops epilepsy. We quantified heart rhythm abnormalities and examined whether the frequency of cardiac events correlated with epileptiform activity, circadian (light/dark) cycle, the presence of seizures, and survival during this period of early epileptogenesis (the development of epilepsy) following SE. Shortly following SE, mice developed an increased interictal heart rate and heart rhythm abnormalities (i.e. sinus pause and sinus arrhythmias) when compared to control mice. Heart rhythm abnormalities were more frequent during the light cycle and were not correlated with increased epileptiform activity or seizure frequency. Finally, SE animals had early mortality, and a death event captured during vEEG recording demonstrated severe bradycardia prior to death. These cardiac changes occurred within 14 days after SE and may represent an early risk factor for sudden death following SE.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>32132552</pmid><doi>10.1038/s41598-020-60324-8</doi><orcidid>https://orcid.org/0000-0001-9934-648X</orcidid><orcidid>https://orcid.org/0000-0002-1878-9631</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | 631/378/1689/178 631/443/376 631/443/592 Animals Arrhythmias, Cardiac - chemically induced Arrhythmias, Cardiac - pathology Arrhythmias, Cardiac - physiopathology Bradycardia Cardiac arrhythmia Circadian Rhythm - drug effects Circadian rhythms Convulsions & seizures Death Disease Models, Animal EEG EKG Electrocardiography Electroencephalography Epilepsy Heart Heart rate Humanities and Social Sciences Kainic Acid - adverse effects Kainic Acid - pharmacology Male Mice Morbidity Mortality multidisciplinary Risk factors Science Science (multidisciplinary) Seizures Sinuses Status Epilepticus - chemically induced Status Epilepticus - physiopathology Tachycardia |
title | Cardiac dysregulation following intrahippocampal kainate-induced status epilepticus |
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