Evaluation of ADD392124 for the Delayed Treatment of Nerve Agent-Induced Status Epilepticus Seizures
ADD392124 was identified by the Anticonvulsant Screening Program as being able to control benzodiazepine-resistant status epilepticus seizures. We evaluated the ability of ADD392124 to control seizures induced by the nerve agent soman. Rats were exposed to a convulsant dose of soman. Seizures were a...
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creator | McDonough, John H Van Shura, Kerry E Lyman, Megan E Eisner, Claire G Mazza, Amelia Kan, Robert K Shih, Tsung-Ming |
description | ADD392124 was identified by the Anticonvulsant Screening Program as being able to control benzodiazepine-resistant status epilepticus seizures. We evaluated the ability of ADD392124 to control seizures induced by the nerve agent soman. Rats were exposed to a convulsant dose of soman. Seizures were allowed to develop, and the standard treatment for nerve agent intoxication--atropine, 2-PAM (an oxime cholinesterase reactivator), and diazepam (a benzodiazepine)--was administered at either 5 or 20 min after seizures started along with ADD392124 at varying doses. ADD392124 was capable of stopping soman-induced seizures at both treatment delay times: anticonvulsant ED50 at the 5-min treatment delay = 256.1 mg/kg (226.3 336.9 mg/kg, 95% confidence limits); anticonvulsant ED50 for the 20-min treatment delay was 325.7 mg/kg (291.3 937.5 mg/kg, 95% confidence limits). The time for seizure termination following administration of ADD392124 at the 5-min treatment delay time was 533.9 sec (8.9 min), while the latency for seizure termination at the 20-min delay was 2258.3 sec (37.6 min). ADD392124 was less potent as an anticonvulsant when compared to anticholinergics, N-methyl-d-aspartate (NMDA) antagonists or benzodiazepines. Nevertheless, ADD392124 was successful in terminating soman-induced seizures at delay times (e.g., 20 min) where few other classes of anticonvulsant drugs have proven effective.
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The original document contains color images.</description><language>eng</language><subject>ANTICONVULSANTS ; Chemical, Biological and Radiological Warfare ; CONVULSIVE DISORDERS ; DELAYED TREATMENT ; GD AGENT ; MEDICAL COUNTERMEASURES ; NERVE AGENTS ; Pharmacology ; SEIZURES ; SOMAN ; THERAPY</subject><creationdate>2011</creationdate><rights>Approved for public release; distribution is unlimited.</rights><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,776,881,27544,27545</link.rule.ids><linktorsrc>$$Uhttps://apps.dtic.mil/sti/citations/ADA555367$$EView_record_in_DTIC$$FView_record_in_$$GDTIC$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>McDonough, John H</creatorcontrib><creatorcontrib>Van Shura, Kerry E</creatorcontrib><creatorcontrib>Lyman, Megan E</creatorcontrib><creatorcontrib>Eisner, Claire G</creatorcontrib><creatorcontrib>Mazza, Amelia</creatorcontrib><creatorcontrib>Kan, Robert K</creatorcontrib><creatorcontrib>Shih, Tsung-Ming</creatorcontrib><creatorcontrib>ARMY MEDICAL RESEARCH INST OF CHEMICAL DEFENSE ABERDEEN PROVING GROUND MD</creatorcontrib><title>Evaluation of ADD392124 for the Delayed Treatment of Nerve Agent-Induced Status Epilepticus Seizures</title><description>ADD392124 was identified by the Anticonvulsant Screening Program as being able to control benzodiazepine-resistant status epilepticus seizures. We evaluated the ability of ADD392124 to control seizures induced by the nerve agent soman. Rats were exposed to a convulsant dose of soman. Seizures were allowed to develop, and the standard treatment for nerve agent intoxication--atropine, 2-PAM (an oxime cholinesterase reactivator), and diazepam (a benzodiazepine)--was administered at either 5 or 20 min after seizures started along with ADD392124 at varying doses. ADD392124 was capable of stopping soman-induced seizures at both treatment delay times: anticonvulsant ED50 at the 5-min treatment delay = 256.1 mg/kg (226.3 336.9 mg/kg, 95% confidence limits); anticonvulsant ED50 for the 20-min treatment delay was 325.7 mg/kg (291.3 937.5 mg/kg, 95% confidence limits). The time for seizure termination following administration of ADD392124 at the 5-min treatment delay time was 533.9 sec (8.9 min), while the latency for seizure termination at the 20-min delay was 2258.3 sec (37.6 min). ADD392124 was less potent as an anticonvulsant when compared to anticholinergics, N-methyl-d-aspartate (NMDA) antagonists or benzodiazepines. Nevertheless, ADD392124 was successful in terminating soman-induced seizures at delay times (e.g., 20 min) where few other classes of anticonvulsant drugs have proven effective.
The original document contains color images.</description><subject>ANTICONVULSANTS</subject><subject>Chemical, Biological and Radiological Warfare</subject><subject>CONVULSIVE DISORDERS</subject><subject>DELAYED TREATMENT</subject><subject>GD AGENT</subject><subject>MEDICAL COUNTERMEASURES</subject><subject>NERVE AGENTS</subject><subject>Pharmacology</subject><subject>SEIZURES</subject><subject>SOMAN</subject><subject>THERAPY</subject><fulltext>true</fulltext><rsrctype>report</rsrctype><creationdate>2011</creationdate><recordtype>report</recordtype><sourceid>1RU</sourceid><recordid>eNqFyrEKwjAUBdAuDqL-gcP7gQ421uIYTEQXl3YvoXnRQExL8lLQrzeCu9O9l3uWhZazckmRHT2MBrgQ7Fjtqj2YMQA9EAQ69UINXUBFT_T0ZTcMMwK_51levU5DBi0pShHkZB1OZIfcW7TvFDCui4VRLuLml6tie5bd6VLq7PpI1iP1XPC6rtmhYX_uDyPQOfY</recordid><startdate>201109</startdate><enddate>201109</enddate><creator>McDonough, John H</creator><creator>Van Shura, Kerry E</creator><creator>Lyman, Megan E</creator><creator>Eisner, Claire G</creator><creator>Mazza, Amelia</creator><creator>Kan, Robert K</creator><creator>Shih, Tsung-Ming</creator><scope>1RU</scope><scope>BHM</scope></search><sort><creationdate>201109</creationdate><title>Evaluation of ADD392124 for the Delayed Treatment of Nerve Agent-Induced Status Epilepticus Seizures</title><author>McDonough, John H ; Van Shura, Kerry E ; Lyman, Megan E ; Eisner, Claire G ; Mazza, Amelia ; Kan, Robert K ; Shih, Tsung-Ming</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-dtic_stinet_ADA5553673</frbrgroupid><rsrctype>reports</rsrctype><prefilter>reports</prefilter><language>eng</language><creationdate>2011</creationdate><topic>ANTICONVULSANTS</topic><topic>Chemical, Biological and Radiological Warfare</topic><topic>CONVULSIVE DISORDERS</topic><topic>DELAYED TREATMENT</topic><topic>GD AGENT</topic><topic>MEDICAL COUNTERMEASURES</topic><topic>NERVE AGENTS</topic><topic>Pharmacology</topic><topic>SEIZURES</topic><topic>SOMAN</topic><topic>THERAPY</topic><toplevel>online_resources</toplevel><creatorcontrib>McDonough, John H</creatorcontrib><creatorcontrib>Van Shura, Kerry E</creatorcontrib><creatorcontrib>Lyman, Megan E</creatorcontrib><creatorcontrib>Eisner, Claire G</creatorcontrib><creatorcontrib>Mazza, Amelia</creatorcontrib><creatorcontrib>Kan, Robert K</creatorcontrib><creatorcontrib>Shih, Tsung-Ming</creatorcontrib><creatorcontrib>ARMY MEDICAL RESEARCH INST OF CHEMICAL DEFENSE ABERDEEN PROVING GROUND MD</creatorcontrib><collection>DTIC Technical Reports</collection><collection>DTIC STINET</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>McDonough, John H</au><au>Van Shura, Kerry E</au><au>Lyman, Megan E</au><au>Eisner, Claire G</au><au>Mazza, Amelia</au><au>Kan, Robert K</au><au>Shih, Tsung-Ming</au><aucorp>ARMY MEDICAL RESEARCH INST OF CHEMICAL DEFENSE ABERDEEN PROVING GROUND MD</aucorp><format>book</format><genre>unknown</genre><ristype>RPRT</ristype><btitle>Evaluation of ADD392124 for the Delayed Treatment of Nerve Agent-Induced Status Epilepticus Seizures</btitle><date>2011-09</date><risdate>2011</risdate><abstract>ADD392124 was identified by the Anticonvulsant Screening Program as being able to control benzodiazepine-resistant status epilepticus seizures. We evaluated the ability of ADD392124 to control seizures induced by the nerve agent soman. Rats were exposed to a convulsant dose of soman. Seizures were allowed to develop, and the standard treatment for nerve agent intoxication--atropine, 2-PAM (an oxime cholinesterase reactivator), and diazepam (a benzodiazepine)--was administered at either 5 or 20 min after seizures started along with ADD392124 at varying doses. ADD392124 was capable of stopping soman-induced seizures at both treatment delay times: anticonvulsant ED50 at the 5-min treatment delay = 256.1 mg/kg (226.3 336.9 mg/kg, 95% confidence limits); anticonvulsant ED50 for the 20-min treatment delay was 325.7 mg/kg (291.3 937.5 mg/kg, 95% confidence limits). The time for seizure termination following administration of ADD392124 at the 5-min treatment delay time was 533.9 sec (8.9 min), while the latency for seizure termination at the 20-min delay was 2258.3 sec (37.6 min). ADD392124 was less potent as an anticonvulsant when compared to anticholinergics, N-methyl-d-aspartate (NMDA) antagonists or benzodiazepines. Nevertheless, ADD392124 was successful in terminating soman-induced seizures at delay times (e.g., 20 min) where few other classes of anticonvulsant drugs have proven effective.
The original document contains color images.</abstract><oa>free_for_read</oa></addata></record> |
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subjects | ANTICONVULSANTS Chemical, Biological and Radiological Warfare CONVULSIVE DISORDERS DELAYED TREATMENT GD AGENT MEDICAL COUNTERMEASURES NERVE AGENTS Pharmacology SEIZURES SOMAN THERAPY |
title | Evaluation of ADD392124 for the Delayed Treatment of Nerve Agent-Induced Status Epilepticus Seizures |
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