Large frequency potentiation induced by 2 Hz stimulation in the hippocampus of epileptic El mice

El mouse has been found to be characteristics with hippocampal disinhibition, and has been suggested decrease in GABAergic synaptic transmission [Ono et al., Brain Res. 745 (1997) 165–172; Fueta et al., Brain Res. 779 (1998) 324–328]. The efficacy of GABAergic synapses can be modulated in response t...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Brain research 1998-05, Vol.792 (1), p.79-88
Hauptverfasser: Fueta, Yukiko, Ohno, Koki, Mita, Takashi
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 88
container_issue 1
container_start_page 79
container_title Brain research
container_volume 792
creator Fueta, Yukiko
Ohno, Koki
Mita, Takashi
description El mouse has been found to be characteristics with hippocampal disinhibition, and has been suggested decrease in GABAergic synaptic transmission [Ono et al., Brain Res. 745 (1997) 165–172; Fueta et al., Brain Res. 779 (1998) 324–328]. The efficacy of GABAergic synapses can be modulated in response to trains of low frequency stimulation. The frequency potentiation of a population spike (PS) and the field excitatory postsynaptic potential (fEPSP) induced by a low frequency stimulation (2 Hz for 15 s) were recorded for the CA3 subfield, and PS alone for the CA1 subfield and dentate gyrus. PS frequency potentiation was greater in El mice than in non-epileptic control ddY mice. Especially the CA3 subfield exhibited a high PS frequency potentiation (300±73%) compared to age-matched ddY mice (64±24%). However, EPSP frequency potentiation was similar in El and ddY mice. The degree of PS frequency potentiation in CA3 was decreased by the reduction of extracellular Ca 2+ from 2 to 1 mM in both strains, suggesting presynaptic involvement. The potentiation in El mice was suppressed by AMPA/kainate type receptor antagonist 6-cyano-7-nitroquinoxaline-2,3-dion (CNQX), but more than half of the control value remained at 5 μM, whereas the potentiation in ddY mice was abolished at this concentration. N-methyl- d-aspartate (NMDA) type receptor antagonist 3-3 (2-carboxypiperazine-4-yl) propyl-1-phosphonate (10 μM; CPP) did not affect the potentiation. Bicuculline (5 μM), GABA A receptor antagonist, did not increase the amplitude of PS during stimulation but induced epileptic (multiple PSs) potentials. High PS frequency potentiation of El mice was mimicked to the degree of that in ddY mice by a low dose of GABA B receptor agonist baclofen (3 μM). The suppression by baclofen was partially reversed by the antagonist saclofen (500 μM). The large frequency potentiation in young El mice, which do not have seizure-susceptibility, indicates an intrinsic property in El mice. It is suggested that the high synchronization of CA3 neurons in El mice is due to a little activation of GABA B receptor activation and also to enhancement of non-NMDA type synaptic transmission.
doi_str_mv 10.1016/S0006-8993(98)00128-0
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_79874853</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0006899398001280</els_id><sourcerecordid>16470037</sourcerecordid><originalsourceid>FETCH-LOGICAL-c352t-d3d70ab2a6f029170e0bae0686d90ef864792e7e67e1ab774b8045ba7c509e913</originalsourceid><addsrcrecordid>eNqFkUtv1DAUhS0EKtPCT6jkBUKwSHttJ36sEKpKizQSi8LaOM4NNcoL20Ga_nrczjDbrq6s892HzyHknMEFAyYv7wBAVtoY8cHojwCM6wpekA3TileS1_CSbI7Ia3Ka0u_yFMLACTkxjRFaiA35uXXxF9I-4p8VJ7-jy5xxysHlME80TN3qsaPtjnJ6-0BTDuM6_Ndovkd6H5Zl9m5c1kTnnuISBlxy8PR6oGPw-Ia86t2Q8O2hnpEfX66_X91W2283X68-bysvGp6rTnQKXMud7IEbpgChdQhSy84A9lrWynBUKBUy1ypVtxrqpnXKN2DQMHFG3u_nLnEuX0nZjiF5HAY34bwmq4xWtW7EsyArq4pPqoDNHvRxTilib5cYRhd3loF9jMA-RWAf_bVG26cILJS-88OCtR2xO3YdPC_6u4PukndDH93kQzpiXIAEzQv2aY9hce1vwGiTDyUi7EJEn203h2cO-QcDOaJ6</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>16470037</pqid></control><display><type>article</type><title>Large frequency potentiation induced by 2 Hz stimulation in the hippocampus of epileptic El mice</title><source>MEDLINE</source><source>Access via ScienceDirect (Elsevier)</source><creator>Fueta, Yukiko ; Ohno, Koki ; Mita, Takashi</creator><creatorcontrib>Fueta, Yukiko ; Ohno, Koki ; Mita, Takashi</creatorcontrib><description>El mouse has been found to be characteristics with hippocampal disinhibition, and has been suggested decrease in GABAergic synaptic transmission [Ono et al., Brain Res. 745 (1997) 165–172; Fueta et al., Brain Res. 779 (1998) 324–328]. The efficacy of GABAergic synapses can be modulated in response to trains of low frequency stimulation. The frequency potentiation of a population spike (PS) and the field excitatory postsynaptic potential (fEPSP) induced by a low frequency stimulation (2 Hz for 15 s) were recorded for the CA3 subfield, and PS alone for the CA1 subfield and dentate gyrus. PS frequency potentiation was greater in El mice than in non-epileptic control ddY mice. Especially the CA3 subfield exhibited a high PS frequency potentiation (300±73%) compared to age-matched ddY mice (64±24%). However, EPSP frequency potentiation was similar in El and ddY mice. The degree of PS frequency potentiation in CA3 was decreased by the reduction of extracellular Ca 2+ from 2 to 1 mM in both strains, suggesting presynaptic involvement. The potentiation in El mice was suppressed by AMPA/kainate type receptor antagonist 6-cyano-7-nitroquinoxaline-2,3-dion (CNQX), but more than half of the control value remained at 5 μM, whereas the potentiation in ddY mice was abolished at this concentration. N-methyl- d-aspartate (NMDA) type receptor antagonist 3-3 (2-carboxypiperazine-4-yl) propyl-1-phosphonate (10 μM; CPP) did not affect the potentiation. Bicuculline (5 μM), GABA A receptor antagonist, did not increase the amplitude of PS during stimulation but induced epileptic (multiple PSs) potentials. High PS frequency potentiation of El mice was mimicked to the degree of that in ddY mice by a low dose of GABA B receptor agonist baclofen (3 μM). The suppression by baclofen was partially reversed by the antagonist saclofen (500 μM). The large frequency potentiation in young El mice, which do not have seizure-susceptibility, indicates an intrinsic property in El mice. It is suggested that the high synchronization of CA3 neurons in El mice is due to a little activation of GABA B receptor activation and also to enhancement of non-NMDA type synaptic transmission.</description><identifier>ISSN: 0006-8993</identifier><identifier>EISSN: 1872-6240</identifier><identifier>DOI: 10.1016/S0006-8993(98)00128-0</identifier><identifier>PMID: 9593833</identifier><identifier>CODEN: BRREAP</identifier><language>eng</language><publisher>London: Elsevier B.V</publisher><subject>Animals ; Biological and medical sciences ; CA3 ; Calcium - metabolism ; Disinhibition ; El mouse ; Electric Stimulation ; Epilepsy - physiopathology ; Excitatory Postsynaptic Potentials - physiology ; Frequency potentiation ; GABA B receptors ; GABA-B Receptor Agonists ; GABA-B Receptor Antagonists ; Headache. Facial pains. Syncopes. Epilepsia. Intracranial hypertension. Brain oedema. Cerebral palsy ; Hippocampus - physiopathology ; In Vitro Techniques ; Medical sciences ; Mice ; Mice, Inbred Strains ; Nervous system (semeiology, syndromes) ; Neurology ; Non-NMDA type glutamate receptors ; Receptors, N-Methyl-D-Aspartate - antagonists &amp; inhibitors ; Synaptic Transmission - drug effects ; Synchronization</subject><ispartof>Brain research, 1998-05, Vol.792 (1), p.79-88</ispartof><rights>1998 Elsevier Science B.V.</rights><rights>1998 INIST-CNRS</rights><rights>Copyright 1998 Elsevier Science B.V.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c352t-d3d70ab2a6f029170e0bae0686d90ef864792e7e67e1ab774b8045ba7c509e913</citedby><cites>FETCH-LOGICAL-c352t-d3d70ab2a6f029170e0bae0686d90ef864792e7e67e1ab774b8045ba7c509e913</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/S0006-8993(98)00128-0$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=2306082$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9593833$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Fueta, Yukiko</creatorcontrib><creatorcontrib>Ohno, Koki</creatorcontrib><creatorcontrib>Mita, Takashi</creatorcontrib><title>Large frequency potentiation induced by 2 Hz stimulation in the hippocampus of epileptic El mice</title><title>Brain research</title><addtitle>Brain Res</addtitle><description>El mouse has been found to be characteristics with hippocampal disinhibition, and has been suggested decrease in GABAergic synaptic transmission [Ono et al., Brain Res. 745 (1997) 165–172; Fueta et al., Brain Res. 779 (1998) 324–328]. The efficacy of GABAergic synapses can be modulated in response to trains of low frequency stimulation. The frequency potentiation of a population spike (PS) and the field excitatory postsynaptic potential (fEPSP) induced by a low frequency stimulation (2 Hz for 15 s) were recorded for the CA3 subfield, and PS alone for the CA1 subfield and dentate gyrus. PS frequency potentiation was greater in El mice than in non-epileptic control ddY mice. Especially the CA3 subfield exhibited a high PS frequency potentiation (300±73%) compared to age-matched ddY mice (64±24%). However, EPSP frequency potentiation was similar in El and ddY mice. The degree of PS frequency potentiation in CA3 was decreased by the reduction of extracellular Ca 2+ from 2 to 1 mM in both strains, suggesting presynaptic involvement. The potentiation in El mice was suppressed by AMPA/kainate type receptor antagonist 6-cyano-7-nitroquinoxaline-2,3-dion (CNQX), but more than half of the control value remained at 5 μM, whereas the potentiation in ddY mice was abolished at this concentration. N-methyl- d-aspartate (NMDA) type receptor antagonist 3-3 (2-carboxypiperazine-4-yl) propyl-1-phosphonate (10 μM; CPP) did not affect the potentiation. Bicuculline (5 μM), GABA A receptor antagonist, did not increase the amplitude of PS during stimulation but induced epileptic (multiple PSs) potentials. High PS frequency potentiation of El mice was mimicked to the degree of that in ddY mice by a low dose of GABA B receptor agonist baclofen (3 μM). The suppression by baclofen was partially reversed by the antagonist saclofen (500 μM). The large frequency potentiation in young El mice, which do not have seizure-susceptibility, indicates an intrinsic property in El mice. It is suggested that the high synchronization of CA3 neurons in El mice is due to a little activation of GABA B receptor activation and also to enhancement of non-NMDA type synaptic transmission.</description><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>CA3</subject><subject>Calcium - metabolism</subject><subject>Disinhibition</subject><subject>El mouse</subject><subject>Electric Stimulation</subject><subject>Epilepsy - physiopathology</subject><subject>Excitatory Postsynaptic Potentials - physiology</subject><subject>Frequency potentiation</subject><subject>GABA B receptors</subject><subject>GABA-B Receptor Agonists</subject><subject>GABA-B Receptor Antagonists</subject><subject>Headache. Facial pains. Syncopes. Epilepsia. Intracranial hypertension. Brain oedema. Cerebral palsy</subject><subject>Hippocampus - physiopathology</subject><subject>In Vitro Techniques</subject><subject>Medical sciences</subject><subject>Mice</subject><subject>Mice, Inbred Strains</subject><subject>Nervous system (semeiology, syndromes)</subject><subject>Neurology</subject><subject>Non-NMDA type glutamate receptors</subject><subject>Receptors, N-Methyl-D-Aspartate - antagonists &amp; inhibitors</subject><subject>Synaptic Transmission - drug effects</subject><subject>Synchronization</subject><issn>0006-8993</issn><issn>1872-6240</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1998</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkUtv1DAUhS0EKtPCT6jkBUKwSHttJ36sEKpKizQSi8LaOM4NNcoL20Ga_nrczjDbrq6s892HzyHknMEFAyYv7wBAVtoY8cHojwCM6wpekA3TileS1_CSbI7Ia3Ka0u_yFMLACTkxjRFaiA35uXXxF9I-4p8VJ7-jy5xxysHlME80TN3qsaPtjnJ6-0BTDuM6_Ndovkd6H5Zl9m5c1kTnnuISBlxy8PR6oGPw-Ia86t2Q8O2hnpEfX66_X91W2283X68-bysvGp6rTnQKXMud7IEbpgChdQhSy84A9lrWynBUKBUy1ypVtxrqpnXKN2DQMHFG3u_nLnEuX0nZjiF5HAY34bwmq4xWtW7EsyArq4pPqoDNHvRxTilib5cYRhd3loF9jMA-RWAf_bVG26cILJS-88OCtR2xO3YdPC_6u4PukndDH93kQzpiXIAEzQv2aY9hce1vwGiTDyUi7EJEn203h2cO-QcDOaJ6</recordid><startdate>19980504</startdate><enddate>19980504</enddate><creator>Fueta, Yukiko</creator><creator>Ohno, Koki</creator><creator>Mita, Takashi</creator><general>Elsevier B.V</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><scope>7X8</scope></search><sort><creationdate>19980504</creationdate><title>Large frequency potentiation induced by 2 Hz stimulation in the hippocampus of epileptic El mice</title><author>Fueta, Yukiko ; Ohno, Koki ; Mita, Takashi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c352t-d3d70ab2a6f029170e0bae0686d90ef864792e7e67e1ab774b8045ba7c509e913</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1998</creationdate><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>CA3</topic><topic>Calcium - metabolism</topic><topic>Disinhibition</topic><topic>El mouse</topic><topic>Electric Stimulation</topic><topic>Epilepsy - physiopathology</topic><topic>Excitatory Postsynaptic Potentials - physiology</topic><topic>Frequency potentiation</topic><topic>GABA B receptors</topic><topic>GABA-B Receptor Agonists</topic><topic>GABA-B Receptor Antagonists</topic><topic>Headache. Facial pains. Syncopes. Epilepsia. Intracranial hypertension. Brain oedema. Cerebral palsy</topic><topic>Hippocampus - physiopathology</topic><topic>In Vitro Techniques</topic><topic>Medical sciences</topic><topic>Mice</topic><topic>Mice, Inbred Strains</topic><topic>Nervous system (semeiology, syndromes)</topic><topic>Neurology</topic><topic>Non-NMDA type glutamate receptors</topic><topic>Receptors, N-Methyl-D-Aspartate - antagonists &amp; inhibitors</topic><topic>Synaptic Transmission - drug effects</topic><topic>Synchronization</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Fueta, Yukiko</creatorcontrib><creatorcontrib>Ohno, Koki</creatorcontrib><creatorcontrib>Mita, Takashi</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><collection>MEDLINE - Academic</collection><jtitle>Brain research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Fueta, Yukiko</au><au>Ohno, Koki</au><au>Mita, Takashi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Large frequency potentiation induced by 2 Hz stimulation in the hippocampus of epileptic El mice</atitle><jtitle>Brain research</jtitle><addtitle>Brain Res</addtitle><date>1998-05-04</date><risdate>1998</risdate><volume>792</volume><issue>1</issue><spage>79</spage><epage>88</epage><pages>79-88</pages><issn>0006-8993</issn><eissn>1872-6240</eissn><coden>BRREAP</coden><abstract>El mouse has been found to be characteristics with hippocampal disinhibition, and has been suggested decrease in GABAergic synaptic transmission [Ono et al., Brain Res. 745 (1997) 165–172; Fueta et al., Brain Res. 779 (1998) 324–328]. The efficacy of GABAergic synapses can be modulated in response to trains of low frequency stimulation. The frequency potentiation of a population spike (PS) and the field excitatory postsynaptic potential (fEPSP) induced by a low frequency stimulation (2 Hz for 15 s) were recorded for the CA3 subfield, and PS alone for the CA1 subfield and dentate gyrus. PS frequency potentiation was greater in El mice than in non-epileptic control ddY mice. Especially the CA3 subfield exhibited a high PS frequency potentiation (300±73%) compared to age-matched ddY mice (64±24%). However, EPSP frequency potentiation was similar in El and ddY mice. The degree of PS frequency potentiation in CA3 was decreased by the reduction of extracellular Ca 2+ from 2 to 1 mM in both strains, suggesting presynaptic involvement. The potentiation in El mice was suppressed by AMPA/kainate type receptor antagonist 6-cyano-7-nitroquinoxaline-2,3-dion (CNQX), but more than half of the control value remained at 5 μM, whereas the potentiation in ddY mice was abolished at this concentration. N-methyl- d-aspartate (NMDA) type receptor antagonist 3-3 (2-carboxypiperazine-4-yl) propyl-1-phosphonate (10 μM; CPP) did not affect the potentiation. Bicuculline (5 μM), GABA A receptor antagonist, did not increase the amplitude of PS during stimulation but induced epileptic (multiple PSs) potentials. High PS frequency potentiation of El mice was mimicked to the degree of that in ddY mice by a low dose of GABA B receptor agonist baclofen (3 μM). The suppression by baclofen was partially reversed by the antagonist saclofen (500 μM). The large frequency potentiation in young El mice, which do not have seizure-susceptibility, indicates an intrinsic property in El mice. It is suggested that the high synchronization of CA3 neurons in El mice is due to a little activation of GABA B receptor activation and also to enhancement of non-NMDA type synaptic transmission.</abstract><cop>London</cop><cop>Amsterdam</cop><cop>New York, NY</cop><pub>Elsevier B.V</pub><pmid>9593833</pmid><doi>10.1016/S0006-8993(98)00128-0</doi><tpages>10</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0006-8993
ispartof Brain research, 1998-05, Vol.792 (1), p.79-88
issn 0006-8993
1872-6240
language eng
recordid cdi_proquest_miscellaneous_79874853
source MEDLINE; Access via ScienceDirect (Elsevier)
subjects Animals
Biological and medical sciences
CA3
Calcium - metabolism
Disinhibition
El mouse
Electric Stimulation
Epilepsy - physiopathology
Excitatory Postsynaptic Potentials - physiology
Frequency potentiation
GABA B receptors
GABA-B Receptor Agonists
GABA-B Receptor Antagonists
Headache. Facial pains. Syncopes. Epilepsia. Intracranial hypertension. Brain oedema. Cerebral palsy
Hippocampus - physiopathology
In Vitro Techniques
Medical sciences
Mice
Mice, Inbred Strains
Nervous system (semeiology, syndromes)
Neurology
Non-NMDA type glutamate receptors
Receptors, N-Methyl-D-Aspartate - antagonists & inhibitors
Synaptic Transmission - drug effects
Synchronization
title Large frequency potentiation induced by 2 Hz stimulation in the hippocampus of epileptic El mice
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-18T17%3A24%3A37IST&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=Large%20frequency%20potentiation%20induced%20by%202%20Hz%20stimulation%20in%20the%20hippocampus%20of%20epileptic%20El%20mice&rft.jtitle=Brain%20research&rft.au=Fueta,%20Yukiko&rft.date=1998-05-04&rft.volume=792&rft.issue=1&rft.spage=79&rft.epage=88&rft.pages=79-88&rft.issn=0006-8993&rft.eissn=1872-6240&rft.coden=BRREAP&rft_id=info:doi/10.1016/S0006-8993(98)00128-0&rft_dat=%3Cproquest_cross%3E16470037%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=16470037&rft_id=info:pmid/9593833&rft_els_id=S0006899398001280&rfr_iscdi=true