Cyclicity of spontaneous recurrent seizures in pilocarpine model of temporal lobe epilepsy in rat
Pilocarpine administration to rats results in status epilepticus (SE) and after a latency period to the occurrence of spontaneous seizures. The model is commonly used to investigate mechanisms of epileptogenesis as well as the antiepileptic effects of novel compounds. Surprisingly, there have been n...
Gespeichert in:
Veröffentlicht in: | Experimental neurology 2007-06, Vol.205 (2), p.501-505 |
---|---|
Hauptverfasser: | , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 505 |
---|---|
container_issue | 2 |
container_start_page | 501 |
container_title | Experimental neurology |
container_volume | 205 |
creator | Goffin, Karolien Nissinen, Jari Van Laere, Koen Pitkänen, Asla |
description | Pilocarpine administration to rats results in status epilepticus (SE) and after a latency period to the occurrence of spontaneous seizures. The model is commonly used to investigate mechanisms of epileptogenesis as well as the antiepileptic effects of novel compounds. Surprisingly, there have been no video-EEG studies determining the duration of latency period from SE to the appearance of the first spontaneous seizures or the type and frequency of spontaneous seizures at early phase of pilocarpine-induced epilepsy even though such information is critical for design of such studies. To address these questions, we induced SE with pilocarpine in 29 adult male Wistar rats with cortical electrodes. Rats were continuously video-EEG monitored during SE and up to 23 days thereafter. The first spontaneous seizures occurred 7.2
±
3.6 days after SE. During the follow-up, the mean daily seizure frequency was 2.6
±
1.9, the mean seizure duration 47
±
7 s, and the mean behavioral seizure score 3.2
±
0.9. Typically first seizures were partial (score 1–2). Interestingly, spontaneous seizures occurred in clusters with cyclicity, peaking every 5 to 8 days. These data show that in the pilocarpine model of temporal lobe epilepsy the latency period is short. Because many of the early seizures are partial and the seizures occur in clusters, the true phenotype of epilepsy triggered by pilocarpine-induced SE may be difficult to characterize without continuous long-term video-EEG monitoring. Finally, our data suggest that the model can be used for studies aiming at identifying the mechanisms of seizure clustering. |
doi_str_mv | 10.1016/j.expneurol.2007.03.008 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_19374038</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0014488607001045</els_id><sourcerecordid>19374038</sourcerecordid><originalsourceid>FETCH-LOGICAL-c496t-70c36314485fc5518e3337b4897a7b7d917c14ed5b3d11f5df2117c825706f643</originalsourceid><addsrcrecordid>eNqFkE1r3DAQhkVoSTYffyHVpbnZHVmyJR_DkjSFQC_NWcjyGLTIlivZIZtfXy27JMeeBobnnY-HkG8MSgas-bEr8W2ecI3BlxWALIGXAOqMbBi0UFSCwxeyAWCiEEo1F-QypR0AtKKS5-SCSSEqDmJDzHZvvbNu2dMw0DSHaTEThjXRiHaNEaeFJnTva8RE3URn54M1cXYT0jH06A-xBcc5ROOpDx1SzAzOaX_Ao1muydfB-IQ3p3pFXh4f_myfiuffP39t758LK9pmKSRY3nAmhKoHW9dMIedcdkK10shO9i2Tlgns6473jA11P1Qst1RVS2iGRvArcnecO8fwd8W06NEli94f_9Gs5VIAVxmUR9DGkFLEQc_RjSbuNQN9sKt3-sOuPtjVwHW2m5O3pxVrN2L_mTvpzMD3E2CSNX6IZrIufXJK8fxak7n7I4dZyKvDqJN1OFnsXda-6D64_x7zD8monb0</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>19374038</pqid></control><display><type>article</type><title>Cyclicity of spontaneous recurrent seizures in pilocarpine model of temporal lobe epilepsy in rat</title><source>MEDLINE</source><source>Elsevier ScienceDirect Journals</source><creator>Goffin, Karolien ; Nissinen, Jari ; Van Laere, Koen ; Pitkänen, Asla</creator><creatorcontrib>Goffin, Karolien ; Nissinen, Jari ; Van Laere, Koen ; Pitkänen, Asla</creatorcontrib><description>Pilocarpine administration to rats results in status epilepticus (SE) and after a latency period to the occurrence of spontaneous seizures. The model is commonly used to investigate mechanisms of epileptogenesis as well as the antiepileptic effects of novel compounds. Surprisingly, there have been no video-EEG studies determining the duration of latency period from SE to the appearance of the first spontaneous seizures or the type and frequency of spontaneous seizures at early phase of pilocarpine-induced epilepsy even though such information is critical for design of such studies. To address these questions, we induced SE with pilocarpine in 29 adult male Wistar rats with cortical electrodes. Rats were continuously video-EEG monitored during SE and up to 23 days thereafter. The first spontaneous seizures occurred 7.2
±
3.6 days after SE. During the follow-up, the mean daily seizure frequency was 2.6
±
1.9, the mean seizure duration 47
±
7 s, and the mean behavioral seizure score 3.2
±
0.9. Typically first seizures were partial (score 1–2). Interestingly, spontaneous seizures occurred in clusters with cyclicity, peaking every 5 to 8 days. These data show that in the pilocarpine model of temporal lobe epilepsy the latency period is short. Because many of the early seizures are partial and the seizures occur in clusters, the true phenotype of epilepsy triggered by pilocarpine-induced SE may be difficult to characterize without continuous long-term video-EEG monitoring. Finally, our data suggest that the model can be used for studies aiming at identifying the mechanisms of seizure clustering.</description><identifier>ISSN: 0014-4886</identifier><identifier>EISSN: 1090-2430</identifier><identifier>DOI: 10.1016/j.expneurol.2007.03.008</identifier><identifier>PMID: 17442304</identifier><identifier>CODEN: EXNEAC</identifier><language>eng</language><publisher>Amsterdam: Elsevier Inc</publisher><subject>Animals ; Behavior, Animal - drug effects ; Biological and medical sciences ; Cyclic pattern ; Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases ; Electroencephalography ; Epilepsy, Temporal Lobe - chemically induced ; Epilepsy, Temporal Lobe - physiopathology ; Headache. Facial pains. Syncopes. Epilepsia. Intracranial hypertension. Brain oedema. Cerebral palsy ; Male ; Medical sciences ; Muscarinic Agonists ; Nervous system (semeiology, syndromes) ; Neurology ; Pilocarpine ; Rats ; Rats, Wistar ; Recurrence ; Seizure clustering ; Seizures - physiopathology ; Spontaneous recurrent seizures ; Status Epilepticus - chemically induced ; Status Epilepticus - physiopathology ; Status Epilepticus - psychology</subject><ispartof>Experimental neurology, 2007-06, Vol.205 (2), p.501-505</ispartof><rights>2007 Elsevier Inc.</rights><rights>2007 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c496t-70c36314485fc5518e3337b4897a7b7d917c14ed5b3d11f5df2117c825706f643</citedby><cites>FETCH-LOGICAL-c496t-70c36314485fc5518e3337b4897a7b7d917c14ed5b3d11f5df2117c825706f643</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0014488607001045$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3536,27903,27904,65309</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=18835516$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17442304$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Goffin, Karolien</creatorcontrib><creatorcontrib>Nissinen, Jari</creatorcontrib><creatorcontrib>Van Laere, Koen</creatorcontrib><creatorcontrib>Pitkänen, Asla</creatorcontrib><title>Cyclicity of spontaneous recurrent seizures in pilocarpine model of temporal lobe epilepsy in rat</title><title>Experimental neurology</title><addtitle>Exp Neurol</addtitle><description>Pilocarpine administration to rats results in status epilepticus (SE) and after a latency period to the occurrence of spontaneous seizures. The model is commonly used to investigate mechanisms of epileptogenesis as well as the antiepileptic effects of novel compounds. Surprisingly, there have been no video-EEG studies determining the duration of latency period from SE to the appearance of the first spontaneous seizures or the type and frequency of spontaneous seizures at early phase of pilocarpine-induced epilepsy even though such information is critical for design of such studies. To address these questions, we induced SE with pilocarpine in 29 adult male Wistar rats with cortical electrodes. Rats were continuously video-EEG monitored during SE and up to 23 days thereafter. The first spontaneous seizures occurred 7.2
±
3.6 days after SE. During the follow-up, the mean daily seizure frequency was 2.6
±
1.9, the mean seizure duration 47
±
7 s, and the mean behavioral seizure score 3.2
±
0.9. Typically first seizures were partial (score 1–2). Interestingly, spontaneous seizures occurred in clusters with cyclicity, peaking every 5 to 8 days. These data show that in the pilocarpine model of temporal lobe epilepsy the latency period is short. Because many of the early seizures are partial and the seizures occur in clusters, the true phenotype of epilepsy triggered by pilocarpine-induced SE may be difficult to characterize without continuous long-term video-EEG monitoring. Finally, our data suggest that the model can be used for studies aiming at identifying the mechanisms of seizure clustering.</description><subject>Animals</subject><subject>Behavior, Animal - drug effects</subject><subject>Biological and medical sciences</subject><subject>Cyclic pattern</subject><subject>Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases</subject><subject>Electroencephalography</subject><subject>Epilepsy, Temporal Lobe - chemically induced</subject><subject>Epilepsy, Temporal Lobe - physiopathology</subject><subject>Headache. Facial pains. Syncopes. Epilepsia. Intracranial hypertension. Brain oedema. Cerebral palsy</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Muscarinic Agonists</subject><subject>Nervous system (semeiology, syndromes)</subject><subject>Neurology</subject><subject>Pilocarpine</subject><subject>Rats</subject><subject>Rats, Wistar</subject><subject>Recurrence</subject><subject>Seizure clustering</subject><subject>Seizures - physiopathology</subject><subject>Spontaneous recurrent seizures</subject><subject>Status Epilepticus - chemically induced</subject><subject>Status Epilepticus - physiopathology</subject><subject>Status Epilepticus - psychology</subject><issn>0014-4886</issn><issn>1090-2430</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkE1r3DAQhkVoSTYffyHVpbnZHVmyJR_DkjSFQC_NWcjyGLTIlivZIZtfXy27JMeeBobnnY-HkG8MSgas-bEr8W2ecI3BlxWALIGXAOqMbBi0UFSCwxeyAWCiEEo1F-QypR0AtKKS5-SCSSEqDmJDzHZvvbNu2dMw0DSHaTEThjXRiHaNEaeFJnTva8RE3URn54M1cXYT0jH06A-xBcc5ROOpDx1SzAzOaX_Ao1muydfB-IQ3p3pFXh4f_myfiuffP39t758LK9pmKSRY3nAmhKoHW9dMIedcdkK10shO9i2Tlgns6473jA11P1Qst1RVS2iGRvArcnecO8fwd8W06NEli94f_9Gs5VIAVxmUR9DGkFLEQc_RjSbuNQN9sKt3-sOuPtjVwHW2m5O3pxVrN2L_mTvpzMD3E2CSNX6IZrIufXJK8fxak7n7I4dZyKvDqJN1OFnsXda-6D64_x7zD8monb0</recordid><startdate>20070601</startdate><enddate>20070601</enddate><creator>Goffin, Karolien</creator><creator>Nissinen, Jari</creator><creator>Van Laere, Koen</creator><creator>Pitkänen, Asla</creator><general>Elsevier Inc</general><general>Elsevier</general><scope>IQODW</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>7TK</scope></search><sort><creationdate>20070601</creationdate><title>Cyclicity of spontaneous recurrent seizures in pilocarpine model of temporal lobe epilepsy in rat</title><author>Goffin, Karolien ; Nissinen, Jari ; Van Laere, Koen ; Pitkänen, Asla</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c496t-70c36314485fc5518e3337b4897a7b7d917c14ed5b3d11f5df2117c825706f643</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>Animals</topic><topic>Behavior, Animal - drug effects</topic><topic>Biological and medical sciences</topic><topic>Cyclic pattern</topic><topic>Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases</topic><topic>Electroencephalography</topic><topic>Epilepsy, Temporal Lobe - chemically induced</topic><topic>Epilepsy, Temporal Lobe - physiopathology</topic><topic>Headache. Facial pains. Syncopes. Epilepsia. Intracranial hypertension. Brain oedema. Cerebral palsy</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Muscarinic Agonists</topic><topic>Nervous system (semeiology, syndromes)</topic><topic>Neurology</topic><topic>Pilocarpine</topic><topic>Rats</topic><topic>Rats, Wistar</topic><topic>Recurrence</topic><topic>Seizure clustering</topic><topic>Seizures - physiopathology</topic><topic>Spontaneous recurrent seizures</topic><topic>Status Epilepticus - chemically induced</topic><topic>Status Epilepticus - physiopathology</topic><topic>Status Epilepticus - psychology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Goffin, Karolien</creatorcontrib><creatorcontrib>Nissinen, Jari</creatorcontrib><creatorcontrib>Van Laere, Koen</creatorcontrib><creatorcontrib>Pitkänen, Asla</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>CrossRef</collection><collection>Neurosciences Abstracts</collection><jtitle>Experimental neurology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Goffin, Karolien</au><au>Nissinen, Jari</au><au>Van Laere, Koen</au><au>Pitkänen, Asla</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Cyclicity of spontaneous recurrent seizures in pilocarpine model of temporal lobe epilepsy in rat</atitle><jtitle>Experimental neurology</jtitle><addtitle>Exp Neurol</addtitle><date>2007-06-01</date><risdate>2007</risdate><volume>205</volume><issue>2</issue><spage>501</spage><epage>505</epage><pages>501-505</pages><issn>0014-4886</issn><eissn>1090-2430</eissn><coden>EXNEAC</coden><abstract>Pilocarpine administration to rats results in status epilepticus (SE) and after a latency period to the occurrence of spontaneous seizures. The model is commonly used to investigate mechanisms of epileptogenesis as well as the antiepileptic effects of novel compounds. Surprisingly, there have been no video-EEG studies determining the duration of latency period from SE to the appearance of the first spontaneous seizures or the type and frequency of spontaneous seizures at early phase of pilocarpine-induced epilepsy even though such information is critical for design of such studies. To address these questions, we induced SE with pilocarpine in 29 adult male Wistar rats with cortical electrodes. Rats were continuously video-EEG monitored during SE and up to 23 days thereafter. The first spontaneous seizures occurred 7.2
±
3.6 days after SE. During the follow-up, the mean daily seizure frequency was 2.6
±
1.9, the mean seizure duration 47
±
7 s, and the mean behavioral seizure score 3.2
±
0.9. Typically first seizures were partial (score 1–2). Interestingly, spontaneous seizures occurred in clusters with cyclicity, peaking every 5 to 8 days. These data show that in the pilocarpine model of temporal lobe epilepsy the latency period is short. Because many of the early seizures are partial and the seizures occur in clusters, the true phenotype of epilepsy triggered by pilocarpine-induced SE may be difficult to characterize without continuous long-term video-EEG monitoring. Finally, our data suggest that the model can be used for studies aiming at identifying the mechanisms of seizure clustering.</abstract><cop>Amsterdam</cop><pub>Elsevier Inc</pub><pmid>17442304</pmid><doi>10.1016/j.expneurol.2007.03.008</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0014-4886 |
ispartof | Experimental neurology, 2007-06, Vol.205 (2), p.501-505 |
issn | 0014-4886 1090-2430 |
language | eng |
recordid | cdi_proquest_miscellaneous_19374038 |
source | MEDLINE; Elsevier ScienceDirect Journals |
subjects | Animals Behavior, Animal - drug effects Biological and medical sciences Cyclic pattern Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases Electroencephalography Epilepsy, Temporal Lobe - chemically induced Epilepsy, Temporal Lobe - physiopathology Headache. Facial pains. Syncopes. Epilepsia. Intracranial hypertension. Brain oedema. Cerebral palsy Male Medical sciences Muscarinic Agonists Nervous system (semeiology, syndromes) Neurology Pilocarpine Rats Rats, Wistar Recurrence Seizure clustering Seizures - physiopathology Spontaneous recurrent seizures Status Epilepticus - chemically induced Status Epilepticus - physiopathology Status Epilepticus - psychology |
title | Cyclicity of spontaneous recurrent seizures in pilocarpine model of temporal lobe epilepsy in rat |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-26T23%3A00%3A26IST&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=Cyclicity%20of%20spontaneous%20recurrent%20seizures%20in%20pilocarpine%20model%20of%20temporal%20lobe%20epilepsy%20in%20rat&rft.jtitle=Experimental%20neurology&rft.au=Goffin,%20Karolien&rft.date=2007-06-01&rft.volume=205&rft.issue=2&rft.spage=501&rft.epage=505&rft.pages=501-505&rft.issn=0014-4886&rft.eissn=1090-2430&rft.coden=EXNEAC&rft_id=info:doi/10.1016/j.expneurol.2007.03.008&rft_dat=%3Cproquest_cross%3E19374038%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=19374038&rft_id=info:pmid/17442304&rft_els_id=S0014488607001045&rfr_iscdi=true |