Electrographic and behavioral indices of ethanol withdrawal sensitization
Behavioral and electrographic measures of CNS hyperexcitability were studied in separate groups of mice undergoing multiple ethanol (EtOH) withdrawals in a well-characterized model of EtOH withdrawal sensitization. Consistent with previous studies from this laboratory, mice experiencing repeated cyc...
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Veröffentlicht in: | Brain research 2002-08, Vol.946 (2), p.272-282 |
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description | Behavioral and electrographic measures of CNS hyperexcitability were studied in separate groups of mice undergoing multiple ethanol (EtOH) withdrawals in a well-characterized model of EtOH withdrawal sensitization. Consistent with previous studies from this laboratory, mice experiencing repeated cycles of EtOH intoxication and withdrawal exhibited significantly more severe withdrawal seizures (handling-induced convulsions, HIC) in comparison to animals tested following a single withdrawal episode. Spontaneous EEG data collected from a separate group of mice undergoing the same EtOH exposure regimen exhibited a highly-typified alteration during EtOH withdrawal wherein normal EEG was abruptly replaced with high-voltage, repetitive spikes in a frequency range of seven to nine spikes per second. This paroxysmal EEG data, termed ‘brief spindle episodes’ (BSE) was virtually absent at baseline (prior to EtOH exposure). However, following withdrawal from chronic EtOH exposure, the percent of the EEG recordings containing BSE increased significantly in a time dependent manner. Moreover, in mice undergoing multiple cycles of EtOH exposure and withdrawal, BSE activity progressively increased over successive withdrawal cycles. In contrast, mice tested after repeated cycles of similar handling in the absence of EtOH exposure did not exhibit significant BSE activity until experiencing their one and only EtOH withdrawal episode. Thus, both behavioral and electrographic signs of EtOH withdrawal-related CNS hyperexcitability increased in magnitude during the course of each withdrawal cycle as well as progressively intensifying over successive withdrawal cycles. |
doi_str_mv | 10.1016/S0006-8993(02)02895-0 |
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Consistent with previous studies from this laboratory, mice experiencing repeated cycles of EtOH intoxication and withdrawal exhibited significantly more severe withdrawal seizures (handling-induced convulsions, HIC) in comparison to animals tested following a single withdrawal episode. Spontaneous EEG data collected from a separate group of mice undergoing the same EtOH exposure regimen exhibited a highly-typified alteration during EtOH withdrawal wherein normal EEG was abruptly replaced with high-voltage, repetitive spikes in a frequency range of seven to nine spikes per second. This paroxysmal EEG data, termed ‘brief spindle episodes’ (BSE) was virtually absent at baseline (prior to EtOH exposure). However, following withdrawal from chronic EtOH exposure, the percent of the EEG recordings containing BSE increased significantly in a time dependent manner. Moreover, in mice undergoing multiple cycles of EtOH exposure and withdrawal, BSE activity progressively increased over successive withdrawal cycles. In contrast, mice tested after repeated cycles of similar handling in the absence of EtOH exposure did not exhibit significant BSE activity until experiencing their one and only EtOH withdrawal episode. Thus, both behavioral and electrographic signs of EtOH withdrawal-related CNS hyperexcitability increased in magnitude during the course of each withdrawal cycle as well as progressively intensifying over successive withdrawal cycles.</description><identifier>ISSN: 0006-8993</identifier><identifier>EISSN: 1872-6240</identifier><identifier>DOI: 10.1016/S0006-8993(02)02895-0</identifier><identifier>PMID: 12137931</identifier><identifier>CODEN: BRREAP</identifier><language>eng</language><publisher>London: Elsevier B.V</publisher><subject>Alcohol withdrawal ; Alcoholism ; Alcoholism and acute alcohol poisoning ; Animals ; Behavior, Animal - drug effects ; Biological and medical sciences ; Body Weight - physiology ; Brief spindle episode ; Central Nervous System Depressants - adverse effects ; Central Nervous System Depressants - blood ; EEG ; Electrodes, Implanted ; Electroencephalography - drug effects ; Electrophysiology ; Ethanol - adverse effects ; Ethanol - blood ; Kindling ; Male ; Medical sciences ; Mice ; Mice, Inbred C3H ; Seizures - physiopathology ; Seizures - psychology ; Sensitization ; Substance Withdrawal Syndrome - physiopathology ; Substance Withdrawal Syndrome - psychology ; Toxicology</subject><ispartof>Brain research, 2002-08, Vol.946 (2), p.272-282</ispartof><rights>2002</rights><rights>2002 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c422t-c1067d03dcdee8a8c37f320be61c576d72dae6769d091f9dd02185b635e6bf8e3</citedby><cites>FETCH-LOGICAL-c422t-c1067d03dcdee8a8c37f320be61c576d72dae6769d091f9dd02185b635e6bf8e3</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(02)02895-0$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=13843395$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12137931$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Veatch, Lynn M.</creatorcontrib><creatorcontrib>Becker, Howard C.</creatorcontrib><title>Electrographic and behavioral indices of ethanol withdrawal sensitization</title><title>Brain research</title><addtitle>Brain Res</addtitle><description>Behavioral and electrographic measures of CNS hyperexcitability were studied in separate groups of mice undergoing multiple ethanol (EtOH) withdrawals in a well-characterized model of EtOH withdrawal sensitization. Consistent with previous studies from this laboratory, mice experiencing repeated cycles of EtOH intoxication and withdrawal exhibited significantly more severe withdrawal seizures (handling-induced convulsions, HIC) in comparison to animals tested following a single withdrawal episode. Spontaneous EEG data collected from a separate group of mice undergoing the same EtOH exposure regimen exhibited a highly-typified alteration during EtOH withdrawal wherein normal EEG was abruptly replaced with high-voltage, repetitive spikes in a frequency range of seven to nine spikes per second. This paroxysmal EEG data, termed ‘brief spindle episodes’ (BSE) was virtually absent at baseline (prior to EtOH exposure). However, following withdrawal from chronic EtOH exposure, the percent of the EEG recordings containing BSE increased significantly in a time dependent manner. Moreover, in mice undergoing multiple cycles of EtOH exposure and withdrawal, BSE activity progressively increased over successive withdrawal cycles. In contrast, mice tested after repeated cycles of similar handling in the absence of EtOH exposure did not exhibit significant BSE activity until experiencing their one and only EtOH withdrawal episode. Thus, both behavioral and electrographic signs of EtOH withdrawal-related CNS hyperexcitability increased in magnitude during the course of each withdrawal cycle as well as progressively intensifying over successive withdrawal cycles.</description><subject>Alcohol withdrawal</subject><subject>Alcoholism</subject><subject>Alcoholism and acute alcohol poisoning</subject><subject>Animals</subject><subject>Behavior, Animal - drug effects</subject><subject>Biological and medical sciences</subject><subject>Body Weight - physiology</subject><subject>Brief spindle episode</subject><subject>Central Nervous System Depressants - adverse effects</subject><subject>Central Nervous System Depressants - blood</subject><subject>EEG</subject><subject>Electrodes, Implanted</subject><subject>Electroencephalography - drug effects</subject><subject>Electrophysiology</subject><subject>Ethanol - adverse effects</subject><subject>Ethanol - blood</subject><subject>Kindling</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Mice</subject><subject>Mice, Inbred C3H</subject><subject>Seizures - physiopathology</subject><subject>Seizures - psychology</subject><subject>Sensitization</subject><subject>Substance Withdrawal Syndrome - physiopathology</subject><subject>Substance Withdrawal Syndrome - psychology</subject><subject>Toxicology</subject><issn>0006-8993</issn><issn>1872-6240</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2002</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkE1LAzEQhoMotn78BGUvih5WJ0k3mz2JFL9A8KCeQzaZtZHtpibbFv31xrbo0dMwzPPODA8hRxQuKFBx-QwAIpdVxc-AnQOTVZHDFhlSWbJcsBFsk-EvMiB7Mb6nlvMKdsmAMsrLitMhebhp0fTBvwU9mziT6c5mNU70wvmg28x11hmMmW8y7Ce68222dP3EBr1M04hddL370r3z3QHZaXQb8XBT98nr7c3L-D5_fLp7GF8_5mbEWJ8bCqK0wK2xiFJLw8uGM6hRUFOUwpbMahSlqCxUtKmsBUZlUQteoKgbiXyfnK73zoL_mGPs1dRFg22rO_TzqKgcFaygPIHFGjTBxxiwUbPgpjp8Kgrqx6FaOVQ_ghQwtXKoIOWONwfm9RTtX2ojLQEnG0BHo9sm6M64-MdxOUqei8RdrTlMOhYOg4rGYWfQupCkK-vdP698Aznsjrs</recordid><startdate>20020816</startdate><enddate>20020816</enddate><creator>Veatch, Lynn M.</creator><creator>Becker, Howard C.</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>7QG</scope><scope>7TK</scope></search><sort><creationdate>20020816</creationdate><title>Electrographic and behavioral indices of ethanol withdrawal sensitization</title><author>Veatch, Lynn M. ; Becker, Howard C.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c422t-c1067d03dcdee8a8c37f320be61c576d72dae6769d091f9dd02185b635e6bf8e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2002</creationdate><topic>Alcohol withdrawal</topic><topic>Alcoholism</topic><topic>Alcoholism and acute alcohol poisoning</topic><topic>Animals</topic><topic>Behavior, Animal - drug effects</topic><topic>Biological and medical sciences</topic><topic>Body Weight - physiology</topic><topic>Brief spindle episode</topic><topic>Central Nervous System Depressants - adverse effects</topic><topic>Central Nervous System Depressants - blood</topic><topic>EEG</topic><topic>Electrodes, Implanted</topic><topic>Electroencephalography - drug effects</topic><topic>Electrophysiology</topic><topic>Ethanol - adverse effects</topic><topic>Ethanol - blood</topic><topic>Kindling</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Mice</topic><topic>Mice, Inbred C3H</topic><topic>Seizures - physiopathology</topic><topic>Seizures - psychology</topic><topic>Sensitization</topic><topic>Substance Withdrawal Syndrome - physiopathology</topic><topic>Substance Withdrawal Syndrome - psychology</topic><topic>Toxicology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Veatch, Lynn M.</creatorcontrib><creatorcontrib>Becker, Howard C.</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>Animal Behavior Abstracts</collection><collection>Neurosciences Abstracts</collection><jtitle>Brain research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Veatch, Lynn M.</au><au>Becker, Howard C.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Electrographic and behavioral indices of ethanol withdrawal sensitization</atitle><jtitle>Brain research</jtitle><addtitle>Brain Res</addtitle><date>2002-08-16</date><risdate>2002</risdate><volume>946</volume><issue>2</issue><spage>272</spage><epage>282</epage><pages>272-282</pages><issn>0006-8993</issn><eissn>1872-6240</eissn><coden>BRREAP</coden><abstract>Behavioral and electrographic measures of CNS hyperexcitability were studied in separate groups of mice undergoing multiple ethanol (EtOH) withdrawals in a well-characterized model of EtOH withdrawal sensitization. Consistent with previous studies from this laboratory, mice experiencing repeated cycles of EtOH intoxication and withdrawal exhibited significantly more severe withdrawal seizures (handling-induced convulsions, HIC) in comparison to animals tested following a single withdrawal episode. Spontaneous EEG data collected from a separate group of mice undergoing the same EtOH exposure regimen exhibited a highly-typified alteration during EtOH withdrawal wherein normal EEG was abruptly replaced with high-voltage, repetitive spikes in a frequency range of seven to nine spikes per second. This paroxysmal EEG data, termed ‘brief spindle episodes’ (BSE) was virtually absent at baseline (prior to EtOH exposure). However, following withdrawal from chronic EtOH exposure, the percent of the EEG recordings containing BSE increased significantly in a time dependent manner. Moreover, in mice undergoing multiple cycles of EtOH exposure and withdrawal, BSE activity progressively increased over successive withdrawal cycles. In contrast, mice tested after repeated cycles of similar handling in the absence of EtOH exposure did not exhibit significant BSE activity until experiencing their one and only EtOH withdrawal episode. Thus, both behavioral and electrographic signs of EtOH withdrawal-related CNS hyperexcitability increased in magnitude during the course of each withdrawal cycle as well as progressively intensifying over successive withdrawal cycles.</abstract><cop>London</cop><cop>Amsterdam</cop><cop>New York, NY</cop><pub>Elsevier B.V</pub><pmid>12137931</pmid><doi>10.1016/S0006-8993(02)02895-0</doi><tpages>11</tpages></addata></record> |
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subjects | Alcohol withdrawal Alcoholism Alcoholism and acute alcohol poisoning Animals Behavior, Animal - drug effects Biological and medical sciences Body Weight - physiology Brief spindle episode Central Nervous System Depressants - adverse effects Central Nervous System Depressants - blood EEG Electrodes, Implanted Electroencephalography - drug effects Electrophysiology Ethanol - adverse effects Ethanol - blood Kindling Male Medical sciences Mice Mice, Inbred C3H Seizures - physiopathology Seizures - psychology Sensitization Substance Withdrawal Syndrome - physiopathology Substance Withdrawal Syndrome - psychology Toxicology |
title | Electrographic and behavioral indices of ethanol withdrawal sensitization |
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