A Possible Role for Gap Junctions in Generation of Very Fast EEG Oscillations Preceding the Onset of, and Perhaps Initiating, Seizures
Purpose: We propose an experimentally and clinically testable hypothesis, concerning the origin of very fast (>∼70 Hz) EEG oscillations that sometimes precede the onset of focal seizures. These oscillations are important, as they may play a causal role in the initiation of seizures. Methods: Subd...
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description | Purpose: We propose an experimentally and clinically testable hypothesis, concerning the origin of very fast (>∼70 Hz) EEG oscillations that sometimes precede the onset of focal seizures. These oscillations are important, as they may play a causal role in the initiation of seizures.
Methods: Subdural EEG recordings were obtained from children with focal cortical dysplasias and intractable seizures. Intra‐ and extracellular recordings were performed in rat hippocampal slices, with induction of population activity, as follows: (a) bath‐applied tetramethylamine (an intracellular alkalinizing agent, that opens gap junctions); (b) bath‐applied carbachol, a cholinergic agonist; and (c) focal pressure ejection of hypertonic K+ solution. Detailed network simulations were performed, the better to understand the cellular mechanisms underlying oscillations. A major feature of the simulations was inclusion of axon–axon gap junctions between principal neurons, as supported by recent experimental data.
Results: Very fast oscillations were found in children before seizure onset, but also superimposed on bursts during the seizure, and on interictal bursts. In slice experiments, very fast oscillations had previously been seen on interictal‐like bursts; we now show such oscillations before, between, and after epileptiform bursts. Very fast oscillations were also seen superimposed on gamma (30–70 Hz) oscillations induced by carbachol or hypertonic K+, and in the latter case, very fast oscillations became continuous when chemical synapses were blocked. Simulations replicate these data, when axonal gap junctions are included.
Conclusions: Electrical coupling between principal neurons, perhaps via axonal gap junctions, could underlie very fast population oscillations, in seizure‐prone brain, but possibly also in normal brain. The anticonvulsant potential of gap‐junction blockers such as carbenoxolone, now in clinical use for treatment of ulcer disease, should be considered. |
doi_str_mv | 10.1046/j.1528-1157.2001.26900.x |
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Methods: Subdural EEG recordings were obtained from children with focal cortical dysplasias and intractable seizures. Intra‐ and extracellular recordings were performed in rat hippocampal slices, with induction of population activity, as follows: (a) bath‐applied tetramethylamine (an intracellular alkalinizing agent, that opens gap junctions); (b) bath‐applied carbachol, a cholinergic agonist; and (c) focal pressure ejection of hypertonic K+ solution. Detailed network simulations were performed, the better to understand the cellular mechanisms underlying oscillations. A major feature of the simulations was inclusion of axon–axon gap junctions between principal neurons, as supported by recent experimental data.
Results: Very fast oscillations were found in children before seizure onset, but also superimposed on bursts during the seizure, and on interictal bursts. In slice experiments, very fast oscillations had previously been seen on interictal‐like bursts; we now show such oscillations before, between, and after epileptiform bursts. Very fast oscillations were also seen superimposed on gamma (30–70 Hz) oscillations induced by carbachol or hypertonic K+, and in the latter case, very fast oscillations became continuous when chemical synapses were blocked. Simulations replicate these data, when axonal gap junctions are included.
Conclusions: Electrical coupling between principal neurons, perhaps via axonal gap junctions, could underlie very fast population oscillations, in seizure‐prone brain, but possibly also in normal brain. The anticonvulsant potential of gap‐junction blockers such as carbenoxolone, now in clinical use for treatment of ulcer disease, should be considered.</description><identifier>ISSN: 0013-9580</identifier><identifier>EISSN: 1528-1167</identifier><identifier>DOI: 10.1046/j.1528-1157.2001.26900.x</identifier><identifier>PMID: 11240585</identifier><identifier>CODEN: EPILAK</identifier><language>eng</language><publisher>Boston, MA, USA: Blackwell Science Inc</publisher><subject>100 Hz ; Animals ; Axons - physiology ; Biological and medical sciences ; Brain - cytology ; Brain - physiopathology ; Carbenoxolone ; Carbenoxolone - pharmacology ; Carbenoxolone - therapeutic use ; Cortical dysplasias ; Depth recordings ; Electrodes, Implanted ; Electroencephalography - statistics & numerical data ; Electrotonic coupling ; Gap Junctions - drug effects ; Gap Junctions - physiology ; Humans ; Medical sciences ; Mice ; Mice, Inbred BALB C ; Microelectrodes ; Nervous system (semeiology, syndromes) ; Nervous system as a whole ; Neurology ; Neurons - physiology ; Rats ; Rats, Wistar ; Seizures - diagnosis ; Seizures - etiology ; Seizures - physiopathology ; Subdural recordings ; Subdural Space ; Videotape Recording</subject><ispartof>Epilepsia (Copenhagen), 2001-02, Vol.42 (2), p.153-170</ispartof><rights>2001 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5390-ee7592af4dd6a959daca6e372bd46d802375ae23a6eab0fe3ce5f0299fe98a5a3</citedby><cites>FETCH-LOGICAL-c5390-ee7592af4dd6a959daca6e372bd46d802375ae23a6eab0fe3ce5f0299fe98a5a3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1046%2Fj.1528-1157.2001.26900.x$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1046%2Fj.1528-1157.2001.26900.x$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,1433,27924,27925,45574,45575,46409,46833</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=907010$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11240585$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Traub, Roger D.</creatorcontrib><creatorcontrib>Whittington, Miles A.</creatorcontrib><creatorcontrib>Buhl, Eberhard H.</creatorcontrib><creatorcontrib>LeBeau, Fiona E. N.</creatorcontrib><creatorcontrib>Bibbig, Andrea</creatorcontrib><creatorcontrib>Boyd, Stewart</creatorcontrib><creatorcontrib>Cross, Helen</creatorcontrib><creatorcontrib>Baldeweg, Torsten</creatorcontrib><title>A Possible Role for Gap Junctions in Generation of Very Fast EEG Oscillations Preceding the Onset of, and Perhaps Initiating, Seizures</title><title>Epilepsia (Copenhagen)</title><addtitle>Epilepsia</addtitle><description>Purpose: We propose an experimentally and clinically testable hypothesis, concerning the origin of very fast (>∼70 Hz) EEG oscillations that sometimes precede the onset of focal seizures. These oscillations are important, as they may play a causal role in the initiation of seizures.
Methods: Subdural EEG recordings were obtained from children with focal cortical dysplasias and intractable seizures. Intra‐ and extracellular recordings were performed in rat hippocampal slices, with induction of population activity, as follows: (a) bath‐applied tetramethylamine (an intracellular alkalinizing agent, that opens gap junctions); (b) bath‐applied carbachol, a cholinergic agonist; and (c) focal pressure ejection of hypertonic K+ solution. Detailed network simulations were performed, the better to understand the cellular mechanisms underlying oscillations. A major feature of the simulations was inclusion of axon–axon gap junctions between principal neurons, as supported by recent experimental data.
Results: Very fast oscillations were found in children before seizure onset, but also superimposed on bursts during the seizure, and on interictal bursts. In slice experiments, very fast oscillations had previously been seen on interictal‐like bursts; we now show such oscillations before, between, and after epileptiform bursts. Very fast oscillations were also seen superimposed on gamma (30–70 Hz) oscillations induced by carbachol or hypertonic K+, and in the latter case, very fast oscillations became continuous when chemical synapses were blocked. Simulations replicate these data, when axonal gap junctions are included.
Conclusions: Electrical coupling between principal neurons, perhaps via axonal gap junctions, could underlie very fast population oscillations, in seizure‐prone brain, but possibly also in normal brain. The anticonvulsant potential of gap‐junction blockers such as carbenoxolone, now in clinical use for treatment of ulcer disease, should be considered.</description><subject>100 Hz</subject><subject>Animals</subject><subject>Axons - physiology</subject><subject>Biological and medical sciences</subject><subject>Brain - cytology</subject><subject>Brain - physiopathology</subject><subject>Carbenoxolone</subject><subject>Carbenoxolone - pharmacology</subject><subject>Carbenoxolone - therapeutic use</subject><subject>Cortical dysplasias</subject><subject>Depth recordings</subject><subject>Electrodes, Implanted</subject><subject>Electroencephalography - statistics & numerical data</subject><subject>Electrotonic coupling</subject><subject>Gap Junctions - drug effects</subject><subject>Gap Junctions - physiology</subject><subject>Humans</subject><subject>Medical sciences</subject><subject>Mice</subject><subject>Mice, Inbred BALB C</subject><subject>Microelectrodes</subject><subject>Nervous system (semeiology, syndromes)</subject><subject>Nervous system as a whole</subject><subject>Neurology</subject><subject>Neurons - physiology</subject><subject>Rats</subject><subject>Rats, Wistar</subject><subject>Seizures - diagnosis</subject><subject>Seizures - etiology</subject><subject>Seizures - physiopathology</subject><subject>Subdural recordings</subject><subject>Subdural Space</subject><subject>Videotape Recording</subject><issn>0013-9580</issn><issn>1528-1167</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2001</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkc2O0zAUhS0EYsrAKyBLSKwm4dquk3iDNBp1StFIrfjbWq5zM-MqdYqdiCkrJDY8J0-CM41gy8Z_9zv3yucQQhnkDObFm13OJK8yxmSZcwCW80IB5PePyGwqFOVjMksVkSlZwRl5FuMOAMqiFE_JGWN8DrKSM_Lrkm66GN22RfqhS0vTBbo0B_p-8LZ3nY_UebpEj8GMV9o19AuGI702saeLxZKuo3Vta07sJqDF2vlb2t8hXfuIfVJcUONrusFwZw6RrrzrXeL97cXvHz8_ovs-BIzPyZPGtBFfTPs5-Xy9-HT1LrtZL1dXlzeZlUJBhlhKxU0zr-vCKKlqY02BouTbel7UFXBRSoNcpEezhQaFRdkAV6pBVRlpxDl5fep7CN3XAWOv9y5aTD_w2A1Rl1AUyTKRwOoE2pAMCtjoQ3B7E46agR5T0Ds9mq3HFPSYgn5IQd8n6ctpxrDdY_1PONmegFcTYKI1bROMty7-5RSUwCBRb0_UN9fi8b_H68Vm9XAUfwDtlKSu</recordid><startdate>200102</startdate><enddate>200102</enddate><creator>Traub, Roger D.</creator><creator>Whittington, Miles A.</creator><creator>Buhl, Eberhard H.</creator><creator>LeBeau, Fiona E. N.</creator><creator>Bibbig, Andrea</creator><creator>Boyd, Stewart</creator><creator>Cross, Helen</creator><creator>Baldeweg, Torsten</creator><general>Blackwell Science Inc</general><general>Blackwell</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>7X8</scope></search><sort><creationdate>200102</creationdate><title>A Possible Role for Gap Junctions in Generation of Very Fast EEG Oscillations Preceding the Onset of, and Perhaps Initiating, Seizures</title><author>Traub, Roger D. ; Whittington, Miles A. ; Buhl, Eberhard H. ; LeBeau, Fiona E. N. ; Bibbig, Andrea ; Boyd, Stewart ; Cross, Helen ; Baldeweg, Torsten</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5390-ee7592af4dd6a959daca6e372bd46d802375ae23a6eab0fe3ce5f0299fe98a5a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2001</creationdate><topic>100 Hz</topic><topic>Animals</topic><topic>Axons - physiology</topic><topic>Biological and medical sciences</topic><topic>Brain - cytology</topic><topic>Brain - physiopathology</topic><topic>Carbenoxolone</topic><topic>Carbenoxolone - pharmacology</topic><topic>Carbenoxolone - therapeutic use</topic><topic>Cortical dysplasias</topic><topic>Depth recordings</topic><topic>Electrodes, Implanted</topic><topic>Electroencephalography - statistics & numerical data</topic><topic>Electrotonic coupling</topic><topic>Gap Junctions - drug effects</topic><topic>Gap Junctions - physiology</topic><topic>Humans</topic><topic>Medical sciences</topic><topic>Mice</topic><topic>Mice, Inbred BALB C</topic><topic>Microelectrodes</topic><topic>Nervous system (semeiology, syndromes)</topic><topic>Nervous system as a whole</topic><topic>Neurology</topic><topic>Neurons - physiology</topic><topic>Rats</topic><topic>Rats, Wistar</topic><topic>Seizures - diagnosis</topic><topic>Seizures - etiology</topic><topic>Seizures - physiopathology</topic><topic>Subdural recordings</topic><topic>Subdural Space</topic><topic>Videotape Recording</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Traub, Roger D.</creatorcontrib><creatorcontrib>Whittington, Miles A.</creatorcontrib><creatorcontrib>Buhl, Eberhard H.</creatorcontrib><creatorcontrib>LeBeau, Fiona E. N.</creatorcontrib><creatorcontrib>Bibbig, Andrea</creatorcontrib><creatorcontrib>Boyd, Stewart</creatorcontrib><creatorcontrib>Cross, Helen</creatorcontrib><creatorcontrib>Baldeweg, Torsten</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>MEDLINE - Academic</collection><jtitle>Epilepsia (Copenhagen)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Traub, Roger D.</au><au>Whittington, Miles A.</au><au>Buhl, Eberhard H.</au><au>LeBeau, Fiona E. N.</au><au>Bibbig, Andrea</au><au>Boyd, Stewart</au><au>Cross, Helen</au><au>Baldeweg, Torsten</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A Possible Role for Gap Junctions in Generation of Very Fast EEG Oscillations Preceding the Onset of, and Perhaps Initiating, Seizures</atitle><jtitle>Epilepsia (Copenhagen)</jtitle><addtitle>Epilepsia</addtitle><date>2001-02</date><risdate>2001</risdate><volume>42</volume><issue>2</issue><spage>153</spage><epage>170</epage><pages>153-170</pages><issn>0013-9580</issn><eissn>1528-1167</eissn><coden>EPILAK</coden><abstract>Purpose: We propose an experimentally and clinically testable hypothesis, concerning the origin of very fast (>∼70 Hz) EEG oscillations that sometimes precede the onset of focal seizures. These oscillations are important, as they may play a causal role in the initiation of seizures.
Methods: Subdural EEG recordings were obtained from children with focal cortical dysplasias and intractable seizures. Intra‐ and extracellular recordings were performed in rat hippocampal slices, with induction of population activity, as follows: (a) bath‐applied tetramethylamine (an intracellular alkalinizing agent, that opens gap junctions); (b) bath‐applied carbachol, a cholinergic agonist; and (c) focal pressure ejection of hypertonic K+ solution. Detailed network simulations were performed, the better to understand the cellular mechanisms underlying oscillations. A major feature of the simulations was inclusion of axon–axon gap junctions between principal neurons, as supported by recent experimental data.
Results: Very fast oscillations were found in children before seizure onset, but also superimposed on bursts during the seizure, and on interictal bursts. In slice experiments, very fast oscillations had previously been seen on interictal‐like bursts; we now show such oscillations before, between, and after epileptiform bursts. Very fast oscillations were also seen superimposed on gamma (30–70 Hz) oscillations induced by carbachol or hypertonic K+, and in the latter case, very fast oscillations became continuous when chemical synapses were blocked. Simulations replicate these data, when axonal gap junctions are included.
Conclusions: Electrical coupling between principal neurons, perhaps via axonal gap junctions, could underlie very fast population oscillations, in seizure‐prone brain, but possibly also in normal brain. The anticonvulsant potential of gap‐junction blockers such as carbenoxolone, now in clinical use for treatment of ulcer disease, should be considered.</abstract><cop>Boston, MA, USA</cop><pub>Blackwell Science Inc</pub><pmid>11240585</pmid><doi>10.1046/j.1528-1157.2001.26900.x</doi><tpages>18</tpages><oa>free_for_read</oa></addata></record> |
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subjects | 100 Hz Animals Axons - physiology Biological and medical sciences Brain - cytology Brain - physiopathology Carbenoxolone Carbenoxolone - pharmacology Carbenoxolone - therapeutic use Cortical dysplasias Depth recordings Electrodes, Implanted Electroencephalography - statistics & numerical data Electrotonic coupling Gap Junctions - drug effects Gap Junctions - physiology Humans Medical sciences Mice Mice, Inbred BALB C Microelectrodes Nervous system (semeiology, syndromes) Nervous system as a whole Neurology Neurons - physiology Rats Rats, Wistar Seizures - diagnosis Seizures - etiology Seizures - physiopathology Subdural recordings Subdural Space Videotape Recording |
title | A Possible Role for Gap Junctions in Generation of Very Fast EEG Oscillations Preceding the Onset of, and Perhaps Initiating, Seizures |
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