Anticonvulsant properties of acetone, a brain ketone elevated by the ketogenic diet
The ketogenic diet (KD), a treatment for drug‐resistant epilepsy, elevates brain acetone. Acetone has been shown to suppress experimental seizures. Whether elevation of acetone is the basis of the anticonvulsant effects of the KD and whether acetone, like the KD, antagonizes many different types of...
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Veröffentlicht in: | Annals of neurology 2003-08, Vol.54 (2), p.219-226 |
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description | The ketogenic diet (KD), a treatment for drug‐resistant epilepsy, elevates brain acetone. Acetone has been shown to suppress experimental seizures. Whether elevation of acetone is the basis of the anticonvulsant effects of the KD and whether acetone, like the KD, antagonizes many different types of seizures, however, is unknown. This study investigated the spectrum of the anticonvulsant effects of acetone in animal seizure models. Rats were injected with acetone intraperitoneally. Dose–response effects were measured in four different models: (1) the maximal electroshock test, which models human tonic‐clonic seizures; (2) the subcutaneous pentylenetetrazole test, which models human typical absence seizures; (3) the amygdala kindling test, which models human complex partial seizures with secondary generalization; and (4) the AY‐9944 test, which models chronic atypical absence seizures, a component of the Lennox–Gastaut syndrome. Acetone suppressed seizures in all of the models, with the following ED50's (expressed in mmol/kg): maximal electroshock, 6.6; pentylenetetrazole, 9.7; generalized kindled seizures, 13.1; focal kindled seizures, 26.5; AY‐9944, 4.0. Acetone appears to have a broad spectrum of anticonvulsant effects. These effects parallel the effects of the KD. Elevation of brain acetone therefore may account for the efficacy of the KD in intractable epilepsy. Ann Neurol 2003 |
doi_str_mv | 10.1002/ana.10634 |
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Carter ; Burnham, W. McIntyre</creator><creatorcontrib>Likhodii, Sergei S. ; Serbanescu, Irina ; Cortez, Miguel A. ; Murphy, Patricia ; Snead III, O. Carter ; Burnham, W. McIntyre</creatorcontrib><description>The ketogenic diet (KD), a treatment for drug‐resistant epilepsy, elevates brain acetone. Acetone has been shown to suppress experimental seizures. Whether elevation of acetone is the basis of the anticonvulsant effects of the KD and whether acetone, like the KD, antagonizes many different types of seizures, however, is unknown. This study investigated the spectrum of the anticonvulsant effects of acetone in animal seizure models. Rats were injected with acetone intraperitoneally. Dose–response effects were measured in four different models: (1) the maximal electroshock test, which models human tonic‐clonic seizures; (2) the subcutaneous pentylenetetrazole test, which models human typical absence seizures; (3) the amygdala kindling test, which models human complex partial seizures with secondary generalization; and (4) the AY‐9944 test, which models chronic atypical absence seizures, a component of the Lennox–Gastaut syndrome. Acetone suppressed seizures in all of the models, with the following ED50's (expressed in mmol/kg): maximal electroshock, 6.6; pentylenetetrazole, 9.7; generalized kindled seizures, 13.1; focal kindled seizures, 26.5; AY‐9944, 4.0. Acetone appears to have a broad spectrum of anticonvulsant effects. These effects parallel the effects of the KD. Elevation of brain acetone therefore may account for the efficacy of the KD in intractable epilepsy. Ann Neurol 2003</description><identifier>ISSN: 0364-5134</identifier><identifier>EISSN: 1531-8249</identifier><identifier>DOI: 10.1002/ana.10634</identifier><identifier>PMID: 12891674</identifier><identifier>CODEN: ANNED3</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Acetone - metabolism ; Acetone - pharmacology ; Amygdala - physiology ; Animals ; Anticonvulsants ; Anticonvulsants. Antiepileptics. Antiparkinson agents ; Ataxia - chemically induced ; Ataxia - psychology ; Biological and medical sciences ; Brain Chemistry - drug effects ; Brain Chemistry - physiology ; Convulsants ; Diabetes Mellitus - diet therapy ; Diet ; Dose-Response Relationship, Drug ; Electroshock ; Epilepsy, Absence - chemically induced ; Epilepsy, Absence - drug therapy ; Epilepsy, Complex Partial - chemically induced ; Epilepsy, Complex Partial - drug therapy ; Epilepsy, Tonic-Clonic - chemically induced ; Epilepsy, Tonic-Clonic - drug therapy ; Kindling, Neurologic - physiology ; Male ; Medical sciences ; Neuropharmacology ; Pentylenetetrazole ; Pharmacology. 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Carter</creatorcontrib><creatorcontrib>Burnham, W. McIntyre</creatorcontrib><title>Anticonvulsant properties of acetone, a brain ketone elevated by the ketogenic diet</title><title>Annals of neurology</title><addtitle>Ann Neurol</addtitle><description>The ketogenic diet (KD), a treatment for drug‐resistant epilepsy, elevates brain acetone. Acetone has been shown to suppress experimental seizures. Whether elevation of acetone is the basis of the anticonvulsant effects of the KD and whether acetone, like the KD, antagonizes many different types of seizures, however, is unknown. This study investigated the spectrum of the anticonvulsant effects of acetone in animal seizure models. Rats were injected with acetone intraperitoneally. Dose–response effects were measured in four different models: (1) the maximal electroshock test, which models human tonic‐clonic seizures; (2) the subcutaneous pentylenetetrazole test, which models human typical absence seizures; (3) the amygdala kindling test, which models human complex partial seizures with secondary generalization; and (4) the AY‐9944 test, which models chronic atypical absence seizures, a component of the Lennox–Gastaut syndrome. Acetone suppressed seizures in all of the models, with the following ED50's (expressed in mmol/kg): maximal electroshock, 6.6; pentylenetetrazole, 9.7; generalized kindled seizures, 13.1; focal kindled seizures, 26.5; AY‐9944, 4.0. Acetone appears to have a broad spectrum of anticonvulsant effects. These effects parallel the effects of the KD. Elevation of brain acetone therefore may account for the efficacy of the KD in intractable epilepsy. Ann Neurol 2003</description><subject>Acetone - metabolism</subject><subject>Acetone - pharmacology</subject><subject>Amygdala - physiology</subject><subject>Animals</subject><subject>Anticonvulsants</subject><subject>Anticonvulsants. Antiepileptics. Antiparkinson agents</subject><subject>Ataxia - chemically induced</subject><subject>Ataxia - psychology</subject><subject>Biological and medical sciences</subject><subject>Brain Chemistry - drug effects</subject><subject>Brain Chemistry - physiology</subject><subject>Convulsants</subject><subject>Diabetes Mellitus - diet therapy</subject><subject>Diet</subject><subject>Dose-Response Relationship, Drug</subject><subject>Electroshock</subject><subject>Epilepsy, Absence - chemically induced</subject><subject>Epilepsy, Absence - drug therapy</subject><subject>Epilepsy, Complex Partial - chemically induced</subject><subject>Epilepsy, Complex Partial - drug therapy</subject><subject>Epilepsy, Tonic-Clonic - chemically induced</subject><subject>Epilepsy, Tonic-Clonic - drug therapy</subject><subject>Kindling, Neurologic - physiology</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Neuropharmacology</subject><subject>Pentylenetetrazole</subject><subject>Pharmacology. 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Carter</creator><creator>Burnham, W. McIntyre</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><general>Willey-Liss</general><scope>BSCLL</scope><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></search><sort><creationdate>200308</creationdate><title>Anticonvulsant properties of acetone, a brain ketone elevated by the ketogenic diet</title><author>Likhodii, Sergei S. ; Serbanescu, Irina ; Cortez, Miguel A. ; Murphy, Patricia ; Snead III, O. Carter ; Burnham, W. McIntyre</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4844-cafec0f9516b9b14e5d963ab3613bb3119f93a5d85ca22c65d5bd911fc00294e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2003</creationdate><topic>Acetone - metabolism</topic><topic>Acetone - pharmacology</topic><topic>Amygdala - physiology</topic><topic>Animals</topic><topic>Anticonvulsants</topic><topic>Anticonvulsants. Antiepileptics. Antiparkinson agents</topic><topic>Ataxia - chemically induced</topic><topic>Ataxia - psychology</topic><topic>Biological and medical sciences</topic><topic>Brain Chemistry - drug effects</topic><topic>Brain Chemistry - physiology</topic><topic>Convulsants</topic><topic>Diabetes Mellitus - diet therapy</topic><topic>Diet</topic><topic>Dose-Response Relationship, Drug</topic><topic>Electroshock</topic><topic>Epilepsy, Absence - chemically induced</topic><topic>Epilepsy, Absence - drug therapy</topic><topic>Epilepsy, Complex Partial - chemically induced</topic><topic>Epilepsy, Complex Partial - drug therapy</topic><topic>Epilepsy, Tonic-Clonic - chemically induced</topic><topic>Epilepsy, Tonic-Clonic - drug therapy</topic><topic>Kindling, Neurologic - physiology</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Neuropharmacology</topic><topic>Pentylenetetrazole</topic><topic>Pharmacology. 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McIntyre</creatorcontrib><collection>Istex</collection><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><jtitle>Annals of neurology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Likhodii, Sergei S.</au><au>Serbanescu, Irina</au><au>Cortez, Miguel A.</au><au>Murphy, Patricia</au><au>Snead III, O. Carter</au><au>Burnham, W. McIntyre</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Anticonvulsant properties of acetone, a brain ketone elevated by the ketogenic diet</atitle><jtitle>Annals of neurology</jtitle><addtitle>Ann Neurol</addtitle><date>2003-08</date><risdate>2003</risdate><volume>54</volume><issue>2</issue><spage>219</spage><epage>226</epage><pages>219-226</pages><issn>0364-5134</issn><eissn>1531-8249</eissn><coden>ANNED3</coden><abstract>The ketogenic diet (KD), a treatment for drug‐resistant epilepsy, elevates brain acetone. Acetone has been shown to suppress experimental seizures. Whether elevation of acetone is the basis of the anticonvulsant effects of the KD and whether acetone, like the KD, antagonizes many different types of seizures, however, is unknown. This study investigated the spectrum of the anticonvulsant effects of acetone in animal seizure models. Rats were injected with acetone intraperitoneally. Dose–response effects were measured in four different models: (1) the maximal electroshock test, which models human tonic‐clonic seizures; (2) the subcutaneous pentylenetetrazole test, which models human typical absence seizures; (3) the amygdala kindling test, which models human complex partial seizures with secondary generalization; and (4) the AY‐9944 test, which models chronic atypical absence seizures, a component of the Lennox–Gastaut syndrome. Acetone suppressed seizures in all of the models, with the following ED50's (expressed in mmol/kg): maximal electroshock, 6.6; pentylenetetrazole, 9.7; generalized kindled seizures, 13.1; focal kindled seizures, 26.5; AY‐9944, 4.0. Acetone appears to have a broad spectrum of anticonvulsant effects. These effects parallel the effects of the KD. Elevation of brain acetone therefore may account for the efficacy of the KD in intractable epilepsy. Ann Neurol 2003</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>12891674</pmid><doi>10.1002/ana.10634</doi><tpages>8</tpages></addata></record> |
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subjects | Acetone - metabolism Acetone - pharmacology Amygdala - physiology Animals Anticonvulsants Anticonvulsants. Antiepileptics. Antiparkinson agents Ataxia - chemically induced Ataxia - psychology Biological and medical sciences Brain Chemistry - drug effects Brain Chemistry - physiology Convulsants Diabetes Mellitus - diet therapy Diet Dose-Response Relationship, Drug Electroshock Epilepsy, Absence - chemically induced Epilepsy, Absence - drug therapy Epilepsy, Complex Partial - chemically induced Epilepsy, Complex Partial - drug therapy Epilepsy, Tonic-Clonic - chemically induced Epilepsy, Tonic-Clonic - drug therapy Kindling, Neurologic - physiology Male Medical sciences Neuropharmacology Pentylenetetrazole Pharmacology. Drug treatments Rats Rats, Wistar trans-1,4-Bis(2-chlorobenzaminomethyl)cyclohexane Dihydrochloride - pharmacology |
title | Anticonvulsant properties of acetone, a brain ketone elevated by the ketogenic diet |
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