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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Hauptverfasser: McDonough, John H, Van Shura, Kerry E, Lyman, Megan E, Eisner, Claire G, Mazza, Amelia, Kan, Robert K, Shih, Tsung-Ming
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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. The original document contains color images.
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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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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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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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