Persistent enhancement of functional MRI responsiveness to sensory stimulation following repeated seizures
Summary Purpose: Neural reorganization and interictal behavioral anomalies have been documented in people with epilepsy and in animal seizure models. Alterations in behavior could be due to somatosensory dysfunction. This study was designed to determine whether seizures can lead to changes in somat...
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Veröffentlicht in: | Epilepsia (Copenhagen) 2011-12, Vol.52 (12), p.2285-2292 |
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creator | Vuong, Jennifer Henderson, Amy K. Tuor, Ursula I. Dunn, Jeff F. Teskey, G. Campbell |
description | Summary
Purpose: Neural reorganization and interictal behavioral anomalies have been documented in people with epilepsy and in animal seizure models. Alterations in behavior could be due to somatosensory dysfunction. This study was designed to determine whether seizures can lead to changes in somatosensory representations and whether those changes are persistent.
Methods: Twice‐daily seizures were elicited by delivering 1 s of electrical stimulation through carbon fiber electrodes implanted in both the corpus callosum and sensorimotor neocortex of young adult male Long‐Evans rats until a total of 20 seizures were elicited. Either 1–3 days or 3–5 weeks following the last seizure, functional magnetic resonance imaging (MRI) was used to image the brain during electrical stimulation of each forepaw independently.
Key Findings: Forepaw stimulation in control rats resulted in a focused and contralateral fMRI signal in the somatosensory neocortex. Rats that had repeated seizures had a 151% increase in the number of voxels activated in the contralateral hemisphere 1–3 days after the last seizure and a 166% increase at 3–5 weeks after the last seizure. The number of voxels activated in response to forepaw stimulation was positively correlated with the duration of the longest seizure experienced by each rat. The intensity of the activated voxels was not significantly increased at either time interval from the last seizure.
Significance: The increased area of activation in somatosensory cortex, which is persistent at 3–5 weeks, is consistent with previous observations of larger motor maps following seizures. Seizure‐induced changes in the functioning of sensory cortex may also contribute to interictal behavioral anomalies. |
doi_str_mv | 10.1111/j.1528-1167.2011.03317.x |
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Purpose: Neural reorganization and interictal behavioral anomalies have been documented in people with epilepsy and in animal seizure models. Alterations in behavior could be due to somatosensory dysfunction. This study was designed to determine whether seizures can lead to changes in somatosensory representations and whether those changes are persistent.
Methods: Twice‐daily seizures were elicited by delivering 1 s of electrical stimulation through carbon fiber electrodes implanted in both the corpus callosum and sensorimotor neocortex of young adult male Long‐Evans rats until a total of 20 seizures were elicited. Either 1–3 days or 3–5 weeks following the last seizure, functional magnetic resonance imaging (MRI) was used to image the brain during electrical stimulation of each forepaw independently.
Key Findings: Forepaw stimulation in control rats resulted in a focused and contralateral fMRI signal in the somatosensory neocortex. Rats that had repeated seizures had a 151% increase in the number of voxels activated in the contralateral hemisphere 1–3 days after the last seizure and a 166% increase at 3–5 weeks after the last seizure. The number of voxels activated in response to forepaw stimulation was positively correlated with the duration of the longest seizure experienced by each rat. The intensity of the activated voxels was not significantly increased at either time interval from the last seizure.
Significance: The increased area of activation in somatosensory cortex, which is persistent at 3–5 weeks, is consistent with previous observations of larger motor maps following seizures. Seizure‐induced changes in the functioning of sensory cortex may also contribute to interictal behavioral anomalies.</description><identifier>ISSN: 0013-9580</identifier><identifier>EISSN: 1528-1167</identifier><identifier>DOI: 10.1111/j.1528-1167.2011.03317.x</identifier><identifier>PMID: 22091536</identifier><identifier>CODEN: EPILAK</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>Afferent Pathways - physiopathology ; Animals ; Behavior ; Biological and medical sciences ; Brain ; Brain mapping ; Carbon ; Corpus callosum ; Corpus Callosum - physiopathology ; Cortex ; Cortex (motor) ; Cortex (somatosensory) ; Electric Stimulation - adverse effects ; Electrical stimuli ; Electrodes ; Electroencephalography ; Epilepsy ; Fibers ; Forelimb - physiopathology ; Forepaw stimulation ; Functional Laterality ; Functional magnetic resonance imaging ; Headache. Facial pains. Syncopes. Epilepsia. Intracranial hypertension. Brain oedema. Cerebral palsy ; Image Processing, Computer-Assisted ; Investigative techniques, diagnostic techniques (general aspects) ; Kindling ; Magnetic Resonance Imaging ; Male ; Medical sciences ; Nervous system ; Nervous system (semeiology, syndromes) ; Neuroimaging ; Neurology ; Oxygen - blood ; Radiodiagnosis. Nmr imagery. Nmr spectrometry ; Rats ; Rats, Long-Evans ; Rodents ; Seizure ; Seizures ; Seizures - etiology ; Seizures - pathology ; Sensorimotor cortex ; sensorimotor system ; Somatosensory Cortex - blood supply ; Somatosensory Cortex - physiopathology ; Time Factors</subject><ispartof>Epilepsia (Copenhagen), 2011-12, Vol.52 (12), p.2285-2292</ispartof><rights>Wiley Periodicals, Inc. © 2011 International League Against Epilepsy</rights><rights>2015 INIST-CNRS</rights><rights>Wiley Periodicals, Inc. © 2011 International League Against Epilepsy.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5257-1d6f4e9fb7c3f7562fe10816321b180bb38e44c6c5acc535a935bf87c3f42bed3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fj.1528-1167.2011.03317.x$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fj.1528-1167.2011.03317.x$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,1427,27901,27902,45550,45551,46384,46808</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=25335489$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22091536$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Vuong, Jennifer</creatorcontrib><creatorcontrib>Henderson, Amy K.</creatorcontrib><creatorcontrib>Tuor, Ursula I.</creatorcontrib><creatorcontrib>Dunn, Jeff F.</creatorcontrib><creatorcontrib>Teskey, G. Campbell</creatorcontrib><title>Persistent enhancement of functional MRI responsiveness to sensory stimulation following repeated seizures</title><title>Epilepsia (Copenhagen)</title><addtitle>Epilepsia</addtitle><description>Summary
Purpose: Neural reorganization and interictal behavioral anomalies have been documented in people with epilepsy and in animal seizure models. Alterations in behavior could be due to somatosensory dysfunction. This study was designed to determine whether seizures can lead to changes in somatosensory representations and whether those changes are persistent.
Methods: Twice‐daily seizures were elicited by delivering 1 s of electrical stimulation through carbon fiber electrodes implanted in both the corpus callosum and sensorimotor neocortex of young adult male Long‐Evans rats until a total of 20 seizures were elicited. Either 1–3 days or 3–5 weeks following the last seizure, functional magnetic resonance imaging (MRI) was used to image the brain during electrical stimulation of each forepaw independently.
Key Findings: Forepaw stimulation in control rats resulted in a focused and contralateral fMRI signal in the somatosensory neocortex. Rats that had repeated seizures had a 151% increase in the number of voxels activated in the contralateral hemisphere 1–3 days after the last seizure and a 166% increase at 3–5 weeks after the last seizure. The number of voxels activated in response to forepaw stimulation was positively correlated with the duration of the longest seizure experienced by each rat. The intensity of the activated voxels was not significantly increased at either time interval from the last seizure.
Significance: The increased area of activation in somatosensory cortex, which is persistent at 3–5 weeks, is consistent with previous observations of larger motor maps following seizures. Seizure‐induced changes in the functioning of sensory cortex may also contribute to interictal behavioral anomalies.</description><subject>Afferent Pathways - physiopathology</subject><subject>Animals</subject><subject>Behavior</subject><subject>Biological and medical sciences</subject><subject>Brain</subject><subject>Brain mapping</subject><subject>Carbon</subject><subject>Corpus callosum</subject><subject>Corpus Callosum - physiopathology</subject><subject>Cortex</subject><subject>Cortex (motor)</subject><subject>Cortex (somatosensory)</subject><subject>Electric Stimulation - adverse effects</subject><subject>Electrical stimuli</subject><subject>Electrodes</subject><subject>Electroencephalography</subject><subject>Epilepsy</subject><subject>Fibers</subject><subject>Forelimb - physiopathology</subject><subject>Forepaw stimulation</subject><subject>Functional Laterality</subject><subject>Functional magnetic resonance imaging</subject><subject>Headache. Facial pains. Syncopes. Epilepsia. Intracranial hypertension. Brain oedema. Cerebral palsy</subject><subject>Image Processing, Computer-Assisted</subject><subject>Investigative techniques, diagnostic techniques (general aspects)</subject><subject>Kindling</subject><subject>Magnetic Resonance Imaging</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Nervous system</subject><subject>Nervous system (semeiology, syndromes)</subject><subject>Neuroimaging</subject><subject>Neurology</subject><subject>Oxygen - blood</subject><subject>Radiodiagnosis. Nmr imagery. Nmr spectrometry</subject><subject>Rats</subject><subject>Rats, Long-Evans</subject><subject>Rodents</subject><subject>Seizure</subject><subject>Seizures</subject><subject>Seizures - etiology</subject><subject>Seizures - pathology</subject><subject>Sensorimotor cortex</subject><subject>sensorimotor system</subject><subject>Somatosensory Cortex - blood supply</subject><subject>Somatosensory Cortex - physiopathology</subject><subject>Time Factors</subject><issn>0013-9580</issn><issn>1528-1167</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqN0UGL1DAUB_AgijuOfgUJiHhqzUuapj14kGXVgRUX0XNIMy-a0iZj0-7u-OlN3XEFT-aSB--XHP5_QiiwEvJ53ZcgeVMA1KrkDKBkQoAqbx-Qzf3iIdkwBqJoZcPOyJOUesaYqpV4TM44Zy1IUW9If4VT8mnGMFMM302wOK5zdNQtwc4-BjPQj593dMJ0iCH5awyYEp0jTRhSnI40zX5cBrNa6uIwxBsfvmV_QDPjPjP_c8mvn5JHzgwJn53uLfn67uLL-Yfi8tP73fnby8JKLlUB-9pV2LpOWeGUrLlDYA3UgkMHDes60WBV2dpKY60U0rRCdq5ZdcU73IsteXX372GKPxZMsx59sjgMJmBckm6hhkpxLv5DyqplXMosX_wj-7hMOZqkgTdCSbEmuyXPT2rpRtzrw-RHMx31n7gzeHkCJlkzuCnn7dNfJ4WQVdNm9-bO3fgBj_d7YHqtX_d6bVmvLeu1fv27fn2rL6526yR-AQDOo9w</recordid><startdate>201112</startdate><enddate>201112</enddate><creator>Vuong, Jennifer</creator><creator>Henderson, Amy K.</creator><creator>Tuor, Ursula I.</creator><creator>Dunn, Jeff F.</creator><creator>Teskey, G. Campbell</creator><general>Blackwell Publishing Ltd</general><general>Wiley-Blackwell</general><general>Wiley Subscription Services, Inc</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7TK</scope><scope>7X8</scope></search><sort><creationdate>201112</creationdate><title>Persistent enhancement of functional MRI responsiveness to sensory stimulation following repeated seizures</title><author>Vuong, Jennifer ; Henderson, Amy K. ; Tuor, Ursula I. ; Dunn, Jeff F. ; Teskey, G. Campbell</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5257-1d6f4e9fb7c3f7562fe10816321b180bb38e44c6c5acc535a935bf87c3f42bed3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Afferent Pathways - physiopathology</topic><topic>Animals</topic><topic>Behavior</topic><topic>Biological and medical sciences</topic><topic>Brain</topic><topic>Brain mapping</topic><topic>Carbon</topic><topic>Corpus callosum</topic><topic>Corpus Callosum - physiopathology</topic><topic>Cortex</topic><topic>Cortex (motor)</topic><topic>Cortex (somatosensory)</topic><topic>Electric Stimulation - adverse effects</topic><topic>Electrical stimuli</topic><topic>Electrodes</topic><topic>Electroencephalography</topic><topic>Epilepsy</topic><topic>Fibers</topic><topic>Forelimb - physiopathology</topic><topic>Forepaw stimulation</topic><topic>Functional Laterality</topic><topic>Functional magnetic resonance imaging</topic><topic>Headache. Facial pains. Syncopes. Epilepsia. Intracranial hypertension. Brain oedema. Cerebral palsy</topic><topic>Image Processing, Computer-Assisted</topic><topic>Investigative techniques, diagnostic techniques (general aspects)</topic><topic>Kindling</topic><topic>Magnetic Resonance Imaging</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Nervous system</topic><topic>Nervous system (semeiology, syndromes)</topic><topic>Neuroimaging</topic><topic>Neurology</topic><topic>Oxygen - blood</topic><topic>Radiodiagnosis. Nmr imagery. Nmr spectrometry</topic><topic>Rats</topic><topic>Rats, Long-Evans</topic><topic>Rodents</topic><topic>Seizure</topic><topic>Seizures</topic><topic>Seizures - etiology</topic><topic>Seizures - pathology</topic><topic>Sensorimotor cortex</topic><topic>sensorimotor system</topic><topic>Somatosensory Cortex - blood supply</topic><topic>Somatosensory Cortex - physiopathology</topic><topic>Time Factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Vuong, Jennifer</creatorcontrib><creatorcontrib>Henderson, Amy K.</creatorcontrib><creatorcontrib>Tuor, Ursula I.</creatorcontrib><creatorcontrib>Dunn, Jeff F.</creatorcontrib><creatorcontrib>Teskey, G. Campbell</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>Neurosciences Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Epilepsia (Copenhagen)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Vuong, Jennifer</au><au>Henderson, Amy K.</au><au>Tuor, Ursula I.</au><au>Dunn, Jeff F.</au><au>Teskey, G. Campbell</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Persistent enhancement of functional MRI responsiveness to sensory stimulation following repeated seizures</atitle><jtitle>Epilepsia (Copenhagen)</jtitle><addtitle>Epilepsia</addtitle><date>2011-12</date><risdate>2011</risdate><volume>52</volume><issue>12</issue><spage>2285</spage><epage>2292</epage><pages>2285-2292</pages><issn>0013-9580</issn><eissn>1528-1167</eissn><coden>EPILAK</coden><abstract>Summary
Purpose: Neural reorganization and interictal behavioral anomalies have been documented in people with epilepsy and in animal seizure models. Alterations in behavior could be due to somatosensory dysfunction. This study was designed to determine whether seizures can lead to changes in somatosensory representations and whether those changes are persistent.
Methods: Twice‐daily seizures were elicited by delivering 1 s of electrical stimulation through carbon fiber electrodes implanted in both the corpus callosum and sensorimotor neocortex of young adult male Long‐Evans rats until a total of 20 seizures were elicited. Either 1–3 days or 3–5 weeks following the last seizure, functional magnetic resonance imaging (MRI) was used to image the brain during electrical stimulation of each forepaw independently.
Key Findings: Forepaw stimulation in control rats resulted in a focused and contralateral fMRI signal in the somatosensory neocortex. Rats that had repeated seizures had a 151% increase in the number of voxels activated in the contralateral hemisphere 1–3 days after the last seizure and a 166% increase at 3–5 weeks after the last seizure. The number of voxels activated in response to forepaw stimulation was positively correlated with the duration of the longest seizure experienced by each rat. The intensity of the activated voxels was not significantly increased at either time interval from the last seizure.
Significance: The increased area of activation in somatosensory cortex, which is persistent at 3–5 weeks, is consistent with previous observations of larger motor maps following seizures. Seizure‐induced changes in the functioning of sensory cortex may also contribute to interictal behavioral anomalies.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>22091536</pmid><doi>10.1111/j.1528-1167.2011.03317.x</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Afferent Pathways - physiopathology Animals Behavior Biological and medical sciences Brain Brain mapping Carbon Corpus callosum Corpus Callosum - physiopathology Cortex Cortex (motor) Cortex (somatosensory) Electric Stimulation - adverse effects Electrical stimuli Electrodes Electroencephalography Epilepsy Fibers Forelimb - physiopathology Forepaw stimulation Functional Laterality Functional magnetic resonance imaging Headache. Facial pains. Syncopes. Epilepsia. Intracranial hypertension. Brain oedema. Cerebral palsy Image Processing, Computer-Assisted Investigative techniques, diagnostic techniques (general aspects) Kindling Magnetic Resonance Imaging Male Medical sciences Nervous system Nervous system (semeiology, syndromes) Neuroimaging Neurology Oxygen - blood Radiodiagnosis. Nmr imagery. Nmr spectrometry Rats Rats, Long-Evans Rodents Seizure Seizures Seizures - etiology Seizures - pathology Sensorimotor cortex sensorimotor system Somatosensory Cortex - blood supply Somatosensory Cortex - physiopathology Time Factors |
title | Persistent enhancement of functional MRI responsiveness to sensory stimulation following repeated seizures |
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