Low levels of sarin affect the eeg in marmoset monkeys: a pilot study
The main purpose of this pilot study was to estimate the lowest observable adverse effect level (LOAEL) for the electroencephalogram (EEG) upon long‐term, low‐level exposure of vehicle‐pretreated and pyridostigmine‐pretreated marmoset monkeys to sarin vapour. This is the C·t value (t = 5 h) of expos...
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Veröffentlicht in: | Journal of applied toxicology 2004-11, Vol.24 (6), p.475-483 |
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description | The main purpose of this pilot study was to estimate the lowest observable adverse effect level (LOAEL) for the electroencephalogram (EEG) upon long‐term, low‐level exposure of vehicle‐pretreated and pyridostigmine‐pretreated marmoset monkeys to sarin vapour. This is the C·t value (t = 5 h) of exposure at which the EEG becomes significantly different from that resulting from air exposure of the same animals. The LOAELs for effects on the EEG in vehicle‐ and pyridostigmine‐pretreated marmosets appeared to be 0.2 and 0.1 mg min m−3, respectively. Comparatively, the latter LOAEL values are at least an order of magnitude lower than the previously established LOAEL for miosis and only 2–5 times higher than the lowest observable effect level (LOEL) of bound sarin in blood.
The second aim of the study was to analyse the EEG of the same marmosets again during a 5‐h exposure to air 1 year after exposure to sarin vapour. All the marmosets still demonstrated significant (P < 0.05) EEG differences. In most vehicle‐pretreated marmosets the energy (µV2) per EEG band was higher than that observed 1 year earlier, which might indicate that neurons had become more sensitive to excitation. This phenomenon was less pronounced in pyridostigmine‐pretreated animals. Visual examination of the EEG records revealed clear bursts of alpha frequencies (ca. 9 Hz), resembling sleep‐spindles, that were present more frequently in both groups of exposed marmosets than in naive animals. These late changes in spindle oscillation might be the result of changes in the cholinergic system due to exposure to sarin vapour 1 year previously.
In conclusion, EEG abnormalities persisting for more than 1 year may occur in humans during long‐term (5 h) exposure to subclinical levels of sarin that are not detectable by the currently fielded alarm systems. Copyright © 2004 John Wiley & Sons, Ltd. |
doi_str_mv | 10.1002/jat.1001 |
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The second aim of the study was to analyse the EEG of the same marmosets again during a 5‐h exposure to air 1 year after exposure to sarin vapour. All the marmosets still demonstrated significant (P < 0.05) EEG differences. In most vehicle‐pretreated marmosets the energy (µV2) per EEG band was higher than that observed 1 year earlier, which might indicate that neurons had become more sensitive to excitation. This phenomenon was less pronounced in pyridostigmine‐pretreated animals. Visual examination of the EEG records revealed clear bursts of alpha frequencies (ca. 9 Hz), resembling sleep‐spindles, that were present more frequently in both groups of exposed marmosets than in naive animals. These late changes in spindle oscillation might be the result of changes in the cholinergic system due to exposure to sarin vapour 1 year previously.
In conclusion, EEG abnormalities persisting for more than 1 year may occur in humans during long‐term (5 h) exposure to subclinical levels of sarin that are not detectable by the currently fielded alarm systems. Copyright © 2004 John Wiley & Sons, Ltd.</description><identifier>ISSN: 0260-437X</identifier><identifier>EISSN: 1099-1263</identifier><identifier>DOI: 10.1002/jat.1001</identifier><identifier>PMID: 15558834</identifier><identifier>CODEN: JJATDK</identifier><language>eng</language><publisher>Chichester, UK: John Wiley & Sons, Ltd</publisher><subject>Animals ; Biological and medical sciences ; Callithrix - physiology ; Chemical and industrial products toxicology. Toxic occupational diseases ; Chemical Warfare Agents - toxicity ; Cholinesterase Inhibitors - administration & dosage ; Cholinesterase Inhibitors - pharmacology ; Dose-Response Relationship, Drug ; EEG ; Electroencephalography - drug effects ; exposure limits ; Female ; Gas, fumes ; Humans ; Inhalation Exposure ; lowest observable adverse effect level (LOAEL) ; Male ; Medical sciences ; nerve agent ; O-isopropyl methylphosphonofluoridate ; pyridostigmine ; Pyridostigmine Bromide - administration & dosage ; Pyridostigmine Bromide - pharmacology ; sarin ; Sarin - administration & dosage ; Sarin - toxicity ; sleep-spindles ; Time Factors ; Toxicology ; whole-body exposure ; field alarm</subject><ispartof>Journal of applied toxicology, 2004-11, Vol.24 (6), p.475-483</ispartof><rights>Copyright © 2004 John Wiley & Sons, Ltd.</rights><rights>2005 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4161-30afa66d35b76ecc95c2fc14098e3485f3d184ea1c59d78456e2ddb51e23ae9c3</citedby><cites>FETCH-LOGICAL-c4161-30afa66d35b76ecc95c2fc14098e3485f3d184ea1c59d78456e2ddb51e23ae9c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fjat.1001$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fjat.1001$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=16298362$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15558834$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>van Helden, Herman P. M.</creatorcontrib><creatorcontrib>Vanwersch, Raymond A. P.</creatorcontrib><creatorcontrib>Kuijpers, Willem C.</creatorcontrib><creatorcontrib>Trap, Henk C.</creatorcontrib><creatorcontrib>Philippens, Ingrid H. C.</creatorcontrib><creatorcontrib>Benschop, Hendrik P.</creatorcontrib><title>Low levels of sarin affect the eeg in marmoset monkeys: a pilot study</title><title>Journal of applied toxicology</title><addtitle>J. Appl. Toxicol</addtitle><description>The main purpose of this pilot study was to estimate the lowest observable adverse effect level (LOAEL) for the electroencephalogram (EEG) upon long‐term, low‐level exposure of vehicle‐pretreated and pyridostigmine‐pretreated marmoset monkeys to sarin vapour. This is the C·t value (t = 5 h) of exposure at which the EEG becomes significantly different from that resulting from air exposure of the same animals. The LOAELs for effects on the EEG in vehicle‐ and pyridostigmine‐pretreated marmosets appeared to be 0.2 and 0.1 mg min m−3, respectively. Comparatively, the latter LOAEL values are at least an order of magnitude lower than the previously established LOAEL for miosis and only 2–5 times higher than the lowest observable effect level (LOEL) of bound sarin in blood.
The second aim of the study was to analyse the EEG of the same marmosets again during a 5‐h exposure to air 1 year after exposure to sarin vapour. All the marmosets still demonstrated significant (P < 0.05) EEG differences. In most vehicle‐pretreated marmosets the energy (µV2) per EEG band was higher than that observed 1 year earlier, which might indicate that neurons had become more sensitive to excitation. This phenomenon was less pronounced in pyridostigmine‐pretreated animals. Visual examination of the EEG records revealed clear bursts of alpha frequencies (ca. 9 Hz), resembling sleep‐spindles, that were present more frequently in both groups of exposed marmosets than in naive animals. These late changes in spindle oscillation might be the result of changes in the cholinergic system due to exposure to sarin vapour 1 year previously.
In conclusion, EEG abnormalities persisting for more than 1 year may occur in humans during long‐term (5 h) exposure to subclinical levels of sarin that are not detectable by the currently fielded alarm systems. Copyright © 2004 John Wiley & Sons, Ltd.</description><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Callithrix - physiology</subject><subject>Chemical and industrial products toxicology. Toxic occupational diseases</subject><subject>Chemical Warfare Agents - toxicity</subject><subject>Cholinesterase Inhibitors - administration & dosage</subject><subject>Cholinesterase Inhibitors - pharmacology</subject><subject>Dose-Response Relationship, Drug</subject><subject>EEG</subject><subject>Electroencephalography - drug effects</subject><subject>exposure limits</subject><subject>Female</subject><subject>Gas, fumes</subject><subject>Humans</subject><subject>Inhalation Exposure</subject><subject>lowest observable adverse effect level (LOAEL)</subject><subject>Male</subject><subject>Medical sciences</subject><subject>nerve agent</subject><subject>O-isopropyl methylphosphonofluoridate</subject><subject>pyridostigmine</subject><subject>Pyridostigmine Bromide - administration & dosage</subject><subject>Pyridostigmine Bromide - pharmacology</subject><subject>sarin</subject><subject>Sarin - administration & dosage</subject><subject>Sarin - toxicity</subject><subject>sleep-spindles</subject><subject>Time Factors</subject><subject>Toxicology</subject><subject>whole-body exposure</subject><subject>field alarm</subject><issn>0260-437X</issn><issn>1099-1263</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp10M9PwjAUB_DGaATRxL_A9KLxMu2Pteu8IUH8gXoQg7emdK862BiuQ-S_d4RFT57ey-sn76VfhI4puaCEsMupqTYN3UFtSuI4oEzyXdQmTJIg5NFbCx14PyWkfmNqH7WoEEIpHrZRf1iscAZfkHlcOOxNmc6xcQ5shasPwADvuJ7kpswLDxXOi_kM1v4KG7xIs6LCvlom60O050zm4aipHfR60x_1boPh8-Cu1x0GNqSSBpwYZ6RMuJhEEqyNhWXO0pDECniohOMJVSEYakWcRCoUEliSTAQFxg3ElnfQ2Xbvoiw-l-ArnafeQpaZORRLr2kkpOIsquH5Ftqy8L4EpxdlWn9irSnRm8h0HdmmoTU9aXYuJzkkf7DJqAanDTDemsyVZm5T_-ckixWXrHbB1q3SDNb_HtT33VFzuPGpr-D715typmXEI6HHTwMdk5fr8QMf6Ef-A2IVkBA</recordid><startdate>200411</startdate><enddate>200411</enddate><creator>van Helden, Herman P. M.</creator><creator>Vanwersch, Raymond A. P.</creator><creator>Kuijpers, Willem C.</creator><creator>Trap, Henk C.</creator><creator>Philippens, Ingrid H. C.</creator><creator>Benschop, Hendrik P.</creator><general>John Wiley & Sons, Ltd</general><general>Wiley</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><scope>7TK</scope><scope>7U7</scope><scope>C1K</scope></search><sort><creationdate>200411</creationdate><title>Low levels of sarin affect the eeg in marmoset monkeys: a pilot study</title><author>van Helden, Herman P. M. ; Vanwersch, Raymond A. P. ; Kuijpers, Willem C. ; Trap, Henk C. ; Philippens, Ingrid H. C. ; Benschop, Hendrik P.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4161-30afa66d35b76ecc95c2fc14098e3485f3d184ea1c59d78456e2ddb51e23ae9c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Callithrix - physiology</topic><topic>Chemical and industrial products toxicology. Toxic occupational diseases</topic><topic>Chemical Warfare Agents - toxicity</topic><topic>Cholinesterase Inhibitors - administration & dosage</topic><topic>Cholinesterase Inhibitors - pharmacology</topic><topic>Dose-Response Relationship, Drug</topic><topic>EEG</topic><topic>Electroencephalography - drug effects</topic><topic>exposure limits</topic><topic>Female</topic><topic>Gas, fumes</topic><topic>Humans</topic><topic>Inhalation Exposure</topic><topic>lowest observable adverse effect level (LOAEL)</topic><topic>Male</topic><topic>Medical sciences</topic><topic>nerve agent</topic><topic>O-isopropyl methylphosphonofluoridate</topic><topic>pyridostigmine</topic><topic>Pyridostigmine Bromide - administration & dosage</topic><topic>Pyridostigmine Bromide - pharmacology</topic><topic>sarin</topic><topic>Sarin - administration & dosage</topic><topic>Sarin - toxicity</topic><topic>sleep-spindles</topic><topic>Time Factors</topic><topic>Toxicology</topic><topic>whole-body exposure</topic><topic>field alarm</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>van Helden, Herman P. M.</creatorcontrib><creatorcontrib>Vanwersch, Raymond A. P.</creatorcontrib><creatorcontrib>Kuijpers, Willem C.</creatorcontrib><creatorcontrib>Trap, Henk C.</creatorcontrib><creatorcontrib>Philippens, Ingrid H. C.</creatorcontrib><creatorcontrib>Benschop, Hendrik P.</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><collection>Neurosciences Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><jtitle>Journal of applied toxicology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>van Helden, Herman P. M.</au><au>Vanwersch, Raymond A. P.</au><au>Kuijpers, Willem C.</au><au>Trap, Henk C.</au><au>Philippens, Ingrid H. C.</au><au>Benschop, Hendrik P.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Low levels of sarin affect the eeg in marmoset monkeys: a pilot study</atitle><jtitle>Journal of applied toxicology</jtitle><addtitle>J. Appl. Toxicol</addtitle><date>2004-11</date><risdate>2004</risdate><volume>24</volume><issue>6</issue><spage>475</spage><epage>483</epage><pages>475-483</pages><issn>0260-437X</issn><eissn>1099-1263</eissn><coden>JJATDK</coden><abstract>The main purpose of this pilot study was to estimate the lowest observable adverse effect level (LOAEL) for the electroencephalogram (EEG) upon long‐term, low‐level exposure of vehicle‐pretreated and pyridostigmine‐pretreated marmoset monkeys to sarin vapour. This is the C·t value (t = 5 h) of exposure at which the EEG becomes significantly different from that resulting from air exposure of the same animals. The LOAELs for effects on the EEG in vehicle‐ and pyridostigmine‐pretreated marmosets appeared to be 0.2 and 0.1 mg min m−3, respectively. Comparatively, the latter LOAEL values are at least an order of magnitude lower than the previously established LOAEL for miosis and only 2–5 times higher than the lowest observable effect level (LOEL) of bound sarin in blood.
The second aim of the study was to analyse the EEG of the same marmosets again during a 5‐h exposure to air 1 year after exposure to sarin vapour. All the marmosets still demonstrated significant (P < 0.05) EEG differences. In most vehicle‐pretreated marmosets the energy (µV2) per EEG band was higher than that observed 1 year earlier, which might indicate that neurons had become more sensitive to excitation. This phenomenon was less pronounced in pyridostigmine‐pretreated animals. Visual examination of the EEG records revealed clear bursts of alpha frequencies (ca. 9 Hz), resembling sleep‐spindles, that were present more frequently in both groups of exposed marmosets than in naive animals. These late changes in spindle oscillation might be the result of changes in the cholinergic system due to exposure to sarin vapour 1 year previously.
In conclusion, EEG abnormalities persisting for more than 1 year may occur in humans during long‐term (5 h) exposure to subclinical levels of sarin that are not detectable by the currently fielded alarm systems. Copyright © 2004 John Wiley & Sons, Ltd.</abstract><cop>Chichester, UK</cop><pub>John Wiley & Sons, Ltd</pub><pmid>15558834</pmid><doi>10.1002/jat.1001</doi><tpages>9</tpages></addata></record> |
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subjects | Animals Biological and medical sciences Callithrix - physiology Chemical and industrial products toxicology. Toxic occupational diseases Chemical Warfare Agents - toxicity Cholinesterase Inhibitors - administration & dosage Cholinesterase Inhibitors - pharmacology Dose-Response Relationship, Drug EEG Electroencephalography - drug effects exposure limits Female Gas, fumes Humans Inhalation Exposure lowest observable adverse effect level (LOAEL) Male Medical sciences nerve agent O-isopropyl methylphosphonofluoridate pyridostigmine Pyridostigmine Bromide - administration & dosage Pyridostigmine Bromide - pharmacology sarin Sarin - administration & dosage Sarin - toxicity sleep-spindles Time Factors Toxicology whole-body exposure field alarm |
title | Low levels of sarin affect the eeg in marmoset monkeys: a pilot study |
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