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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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/ |
work_keys_str_mv |
AT jirikassa theinfluenceofoximeselectionontheefficacyofantidotaltreatmentofsomanpoisonedrats AT joseffusek theinfluenceofoximeselectionontheefficacyofantidotaltreatmentofsomanpoisonedrats AT jirikassa influenceofoximeselectionontheefficacyofantidotaltreatmentofsomanpoisonedrats AT joseffusek influenceofoximeselectionontheefficacyofantidotaltreatmentofsomanpoisonedrats |
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