The Influence of Oxime Selection on the Efficacy of Antidotal Treatment of Soman-Poisoned Rats

1. The influence of some acetylcholinesterase reactivators (HI-6, obidoxime, pralidoxime) on the efficacy of antidotal treatment to eliminate soman-induced disturbance of respiration and circulation and to protect experimental animals poisoned with supralethal dose of soman (1.5 × LD50) was investig...

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Main Authors: Jiří Kassa, Josef Fusek
Format: Article
Language:English
Published: Karolinum Press 2002-01-01
Series:Acta Medica
Subjects:
Rat
Online Access:https://actamedica.lfhk.cuni.cz/45/1/0019/
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spelling doaj-3c658069ee10483990c2f0f2bbe6ac5b2020-11-25T00:01:30ZengKarolinum PressActa Medica1211-42861805-96942002-01-01451192710.14712/18059694.2019.52The Influence of Oxime Selection on the Efficacy of Antidotal Treatment of Soman-Poisoned RatsJiří Kassa0Josef Fusek1Purkyně Military Medical Academy, Department of Toxicology, Hradec Králové, Czech RepublicPurkyně Military Medical Academy, Department of Toxicology, Hradec Králové, Czech Republic1. The influence of some acetylcholinesterase reactivators (HI-6, obidoxime, pralidoxime) on the efficacy of antidotal treatment to eliminate soman-induced disturbance of respiration and circulation and to protect experimental animals poisoned with supralethal dose of soman (1.5 × LD50) was investigated in a rat model with on-line monitoring of respiratory and circulatory parameters. 2. Obidoxime or pralidoxime in combination with atropine were insufficient to enable soman-poisoned rats to survive for 2 hours when given 1 minute after the administration of soman. 3. On the other hand, the ability of the oxime HI-6 in combination with atropine to prevent soman-induced alteration of respiration and circulation was significantly higher. Some rats treated with HI-6 in combination with atropine were fully protected against the lethal toxic effects of soman within 2 hours following soman administration. 4. Our findings confirm that the oxime HI-6 seems to be a much more suitable and efficacious acetylcholinesterase reactivator for the antidotal treatment of severe acute soman-induced poisoning than currently used obidoxime or pralidoxime.https://actamedica.lfhk.cuni.cz/45/1/0019/SomanAtropineHI-6ObidoximePralidoximeRat
collection DOAJ
language English
format Article
sources DOAJ
author Jiří Kassa
Josef Fusek
spellingShingle Jiří Kassa
Josef Fusek
The Influence of Oxime Selection on the Efficacy of Antidotal Treatment of Soman-Poisoned Rats
Acta Medica
Soman
Atropine
HI-6
Obidoxime
Pralidoxime
Rat
author_facet Jiří Kassa
Josef Fusek
author_sort Jiří Kassa
title The Influence of Oxime Selection on the Efficacy of Antidotal Treatment of Soman-Poisoned Rats
title_short The Influence of Oxime Selection on the Efficacy of Antidotal Treatment of Soman-Poisoned Rats
title_full The Influence of Oxime Selection on the Efficacy of Antidotal Treatment of Soman-Poisoned Rats
title_fullStr The Influence of Oxime Selection on the Efficacy of Antidotal Treatment of Soman-Poisoned Rats
title_full_unstemmed The Influence of Oxime Selection on the Efficacy of Antidotal Treatment of Soman-Poisoned Rats
title_sort influence of oxime selection on the efficacy of antidotal treatment of soman-poisoned rats
publisher Karolinum Press
series Acta Medica
issn 1211-4286
1805-9694
publishDate 2002-01-01
description 1. The influence of some acetylcholinesterase reactivators (HI-6, obidoxime, pralidoxime) on the efficacy of antidotal treatment to eliminate soman-induced disturbance of respiration and circulation and to protect experimental animals poisoned with supralethal dose of soman (1.5 × LD50) was investigated in a rat model with on-line monitoring of respiratory and circulatory parameters. 2. Obidoxime or pralidoxime in combination with atropine were insufficient to enable soman-poisoned rats to survive for 2 hours when given 1 minute after the administration of soman. 3. On the other hand, the ability of the oxime HI-6 in combination with atropine to prevent soman-induced alteration of respiration and circulation was significantly higher. Some rats treated with HI-6 in combination with atropine were fully protected against the lethal toxic effects of soman within 2 hours following soman administration. 4. Our findings confirm that the oxime HI-6 seems to be a much more suitable and efficacious acetylcholinesterase reactivator for the antidotal treatment of severe acute soman-induced poisoning than currently used obidoxime or pralidoxime.
topic Soman
Atropine
HI-6
Obidoxime
Pralidoxime
Rat
url https://actamedica.lfhk.cuni.cz/45/1/0019/
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