Timing of ketogenic diet initiation in an experimental epilepsy model
Following kainic acid (KA)-induced status epilepticus (SE), the ketogenic diet (KD) retards the development of epileptogenesis, with fewer spontaneous recurrent seizures (SRS) and less mossy fiber sprouting than rats on a normal diet. In this study, we investigated whether there is a critical period...
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creator | Su, Sharon W. Cilio, M.Roberta Sogawa, Yoshimi Silveira, Diosely Holmes, Gregory L. Stafstrom, Carl E. |
description | Following kainic acid (KA)-induced status epilepticus (SE), the ketogenic diet (KD) retards the development of epileptogenesis, with fewer spontaneous recurrent seizures (SRS) and less mossy fiber sprouting than rats on a normal diet. In this study, we investigated whether there is a critical period for initiation of the KD, in terms of the diet’s effectiveness in reducing SRS. In addition, we investigated whether early treatment with the KD prevents the deficits in spatial learning and memory that ordinarily follow KA-induced SE. Young rats (P30) underwent KA-induced SE, followed by assignment to one of three treatment groups: control diet (‘KA’), KD begun 2 days after SE (‘KD2’), and KD begun fourteen days after SE (‘KD14’). For 12 weeks following SE, rats were monitored by closed circuit video recording (12 h/wk) to detect SRS. KD2 rats had significantly fewer SRS than rats in the control or KD14 groups. On water maze testing to assess spatial learning and memory, KD2 rats had significantly poorer acquisition of place learning than control (KA alone) or KD14 rats. KD2 rats also failed to gain weight well. There was no difference between groups on routine histologic examination of the hippocampus. In summary, P30 rats placed on the KD 2 days after SE were relatively protected from recurrent seizures, but showed behavioral and physical impairment. Rats placed on the KD 14 days after KA-induced SE did not differ from controls with regard to spontaneous seizure rate. |
doi_str_mv | 10.1016/S0165-3806(00)00130-9 |
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In this study, we investigated whether there is a critical period for initiation of the KD, in terms of the diet’s effectiveness in reducing SRS. In addition, we investigated whether early treatment with the KD prevents the deficits in spatial learning and memory that ordinarily follow KA-induced SE. Young rats (P30) underwent KA-induced SE, followed by assignment to one of three treatment groups: control diet (‘KA’), KD begun 2 days after SE (‘KD2’), and KD begun fourteen days after SE (‘KD14’). For 12 weeks following SE, rats were monitored by closed circuit video recording (12 h/wk) to detect SRS. KD2 rats had significantly fewer SRS than rats in the control or KD14 groups. On water maze testing to assess spatial learning and memory, KD2 rats had significantly poorer acquisition of place learning than control (KA alone) or KD14 rats. KD2 rats also failed to gain weight well. There was no difference between groups on routine histologic examination of the hippocampus. In summary, P30 rats placed on the KD 2 days after SE were relatively protected from recurrent seizures, but showed behavioral and physical impairment. Rats placed on the KD 14 days after KA-induced SE did not differ from controls with regard to spontaneous seizure rate.</description><identifier>ISSN: 0165-3806</identifier><identifier>DOI: 10.1016/S0165-3806(00)00130-9</identifier><identifier>PMID: 11154768</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Animal model ; Animals ; Brain - growth & development ; Brain - physiopathology ; Diet, Protein-Restricted ; Dietary Carbohydrates - pharmacology ; Dietary Fats - pharmacology ; Epilepsy ; Excitatory Amino Acid Antagonists ; Kainic Acid ; Ketogenic diet ; Ketosis - etiology ; Male ; Maze Learning - drug effects ; Rats ; Rats, Sprague-Dawley ; Seizures - chemically induced ; Seizures - diet therapy ; Seizures - physiopathology ; Spontaneous recurrent seizure ; Status Epilepticus - chemically induced ; Status Epilepticus - diet therapy ; Status Epilepticus - physiopathology ; β-Hydroxybutyrate</subject><ispartof>Brain research. Developmental brain research, 2000-12, Vol.125 (1), p.131-138</ispartof><rights>2000 Elsevier Science B.V.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c444t-75c429cca5bb109c3110822acb9db12405d0eea12816cece64800c2f3e269dbc3</citedby><cites>FETCH-LOGICAL-c444t-75c429cca5bb109c3110822acb9db12405d0eea12816cece64800c2f3e269dbc3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27923,27924</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11154768$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Su, Sharon W.</creatorcontrib><creatorcontrib>Cilio, M.Roberta</creatorcontrib><creatorcontrib>Sogawa, Yoshimi</creatorcontrib><creatorcontrib>Silveira, Diosely</creatorcontrib><creatorcontrib>Holmes, Gregory L.</creatorcontrib><creatorcontrib>Stafstrom, Carl E.</creatorcontrib><title>Timing of ketogenic diet initiation in an experimental epilepsy model</title><title>Brain research. Developmental brain research</title><addtitle>Brain Res Dev Brain Res</addtitle><description>Following kainic acid (KA)-induced status epilepticus (SE), the ketogenic diet (KD) retards the development of epileptogenesis, with fewer spontaneous recurrent seizures (SRS) and less mossy fiber sprouting than rats on a normal diet. In this study, we investigated whether there is a critical period for initiation of the KD, in terms of the diet’s effectiveness in reducing SRS. In addition, we investigated whether early treatment with the KD prevents the deficits in spatial learning and memory that ordinarily follow KA-induced SE. Young rats (P30) underwent KA-induced SE, followed by assignment to one of three treatment groups: control diet (‘KA’), KD begun 2 days after SE (‘KD2’), and KD begun fourteen days after SE (‘KD14’). For 12 weeks following SE, rats were monitored by closed circuit video recording (12 h/wk) to detect SRS. KD2 rats had significantly fewer SRS than rats in the control or KD14 groups. On water maze testing to assess spatial learning and memory, KD2 rats had significantly poorer acquisition of place learning than control (KA alone) or KD14 rats. KD2 rats also failed to gain weight well. There was no difference between groups on routine histologic examination of the hippocampus. In summary, P30 rats placed on the KD 2 days after SE were relatively protected from recurrent seizures, but showed behavioral and physical impairment. Rats placed on the KD 14 days after KA-induced SE did not differ from controls with regard to spontaneous seizure rate.</description><subject>Animal model</subject><subject>Animals</subject><subject>Brain - growth & development</subject><subject>Brain - physiopathology</subject><subject>Diet, Protein-Restricted</subject><subject>Dietary Carbohydrates - pharmacology</subject><subject>Dietary Fats - pharmacology</subject><subject>Epilepsy</subject><subject>Excitatory Amino Acid Antagonists</subject><subject>Kainic Acid</subject><subject>Ketogenic diet</subject><subject>Ketosis - etiology</subject><subject>Male</subject><subject>Maze Learning - drug effects</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Seizures - chemically induced</subject><subject>Seizures - diet therapy</subject><subject>Seizures - physiopathology</subject><subject>Spontaneous recurrent seizure</subject><subject>Status Epilepticus - chemically induced</subject><subject>Status Epilepticus - diet therapy</subject><subject>Status Epilepticus - physiopathology</subject><subject>β-Hydroxybutyrate</subject><issn>0165-3806</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2000</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkEtPwzAMgHMAMRj8BFBPCA4Fu01fJ4Sm8ZAmcWCcozT1pkCblCZD7N-TPQRHLo7lfLaTj7FzhBsEzG9fQ8jitIT8CuAaAFOIqwN2_FsesRPn3mFzU-IRGyFixou8PGbTue60WUZ2EX2Qt0syWkWNJh9po72WXlsT0kiaiL57GnRHxss2ol631Lt11NmG2lN2uJCto7P9OWZvD9P55CmevTw-T-5nseKc-7jIFE8qpWRW1wiVShGhTBKp6qqpMeGQNUAkMSkxV6Qo5yWAShYpJXkgVDpml7u5_WA_V-S86LRT1LbSkF05gUVRpLzCAGY7UA3WuYEWog9Pl8NaIIiNM7F1JjZyBIDYOhNV6LvYL1jVHTV_XXthAbjbARS--aVpEE5pMooaPZDyorH6nxU_7Ed9qg</recordid><startdate>20001229</startdate><enddate>20001229</enddate><creator>Su, Sharon W.</creator><creator>Cilio, M.Roberta</creator><creator>Sogawa, Yoshimi</creator><creator>Silveira, Diosely</creator><creator>Holmes, Gregory L.</creator><creator>Stafstrom, Carl E.</creator><general>Elsevier B.V</general><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>20001229</creationdate><title>Timing of ketogenic diet initiation in an experimental epilepsy model</title><author>Su, Sharon W. ; Cilio, M.Roberta ; Sogawa, Yoshimi ; Silveira, Diosely ; Holmes, Gregory L. ; Stafstrom, Carl E.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c444t-75c429cca5bb109c3110822acb9db12405d0eea12816cece64800c2f3e269dbc3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2000</creationdate><topic>Animal model</topic><topic>Animals</topic><topic>Brain - growth & development</topic><topic>Brain - physiopathology</topic><topic>Diet, Protein-Restricted</topic><topic>Dietary Carbohydrates - pharmacology</topic><topic>Dietary Fats - pharmacology</topic><topic>Epilepsy</topic><topic>Excitatory Amino Acid Antagonists</topic><topic>Kainic Acid</topic><topic>Ketogenic diet</topic><topic>Ketosis - etiology</topic><topic>Male</topic><topic>Maze Learning - drug effects</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Seizures - chemically induced</topic><topic>Seizures - diet therapy</topic><topic>Seizures - physiopathology</topic><topic>Spontaneous recurrent seizure</topic><topic>Status Epilepticus - chemically induced</topic><topic>Status Epilepticus - diet therapy</topic><topic>Status Epilepticus - physiopathology</topic><topic>β-Hydroxybutyrate</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Su, Sharon W.</creatorcontrib><creatorcontrib>Cilio, M.Roberta</creatorcontrib><creatorcontrib>Sogawa, Yoshimi</creatorcontrib><creatorcontrib>Silveira, Diosely</creatorcontrib><creatorcontrib>Holmes, Gregory L.</creatorcontrib><creatorcontrib>Stafstrom, Carl E.</creatorcontrib><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>Brain research. Developmental brain research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Su, Sharon W.</au><au>Cilio, M.Roberta</au><au>Sogawa, Yoshimi</au><au>Silveira, Diosely</au><au>Holmes, Gregory L.</au><au>Stafstrom, Carl E.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Timing of ketogenic diet initiation in an experimental epilepsy model</atitle><jtitle>Brain research. Developmental brain research</jtitle><addtitle>Brain Res Dev Brain Res</addtitle><date>2000-12-29</date><risdate>2000</risdate><volume>125</volume><issue>1</issue><spage>131</spage><epage>138</epage><pages>131-138</pages><issn>0165-3806</issn><abstract>Following kainic acid (KA)-induced status epilepticus (SE), the ketogenic diet (KD) retards the development of epileptogenesis, with fewer spontaneous recurrent seizures (SRS) and less mossy fiber sprouting than rats on a normal diet. In this study, we investigated whether there is a critical period for initiation of the KD, in terms of the diet’s effectiveness in reducing SRS. In addition, we investigated whether early treatment with the KD prevents the deficits in spatial learning and memory that ordinarily follow KA-induced SE. Young rats (P30) underwent KA-induced SE, followed by assignment to one of three treatment groups: control diet (‘KA’), KD begun 2 days after SE (‘KD2’), and KD begun fourteen days after SE (‘KD14’). For 12 weeks following SE, rats were monitored by closed circuit video recording (12 h/wk) to detect SRS. KD2 rats had significantly fewer SRS than rats in the control or KD14 groups. On water maze testing to assess spatial learning and memory, KD2 rats had significantly poorer acquisition of place learning than control (KA alone) or KD14 rats. KD2 rats also failed to gain weight well. There was no difference between groups on routine histologic examination of the hippocampus. In summary, P30 rats placed on the KD 2 days after SE were relatively protected from recurrent seizures, but showed behavioral and physical impairment. Rats placed on the KD 14 days after KA-induced SE did not differ from controls with regard to spontaneous seizure rate.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>11154768</pmid><doi>10.1016/S0165-3806(00)00130-9</doi><tpages>8</tpages></addata></record> |
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subjects | Animal model Animals Brain - growth & development Brain - physiopathology Diet, Protein-Restricted Dietary Carbohydrates - pharmacology Dietary Fats - pharmacology Epilepsy Excitatory Amino Acid Antagonists Kainic Acid Ketogenic diet Ketosis - etiology Male Maze Learning - drug effects Rats Rats, Sprague-Dawley Seizures - chemically induced Seizures - diet therapy Seizures - physiopathology Spontaneous recurrent seizure Status Epilepticus - chemically induced Status Epilepticus - diet therapy Status Epilepticus - physiopathology β-Hydroxybutyrate |
title | Timing of ketogenic diet initiation in an experimental epilepsy model |
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