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Description
  • The neuroprotective effects of a newly developed oxime K203 and currently available oximes (obidoxime, HI-6) in combination with atropine in rats poisoned with sarin were studied. The sarin-induced neurotoxicity was monitored using a functional observatory battery at 2 similar to hr after sarin challenge. The results indicate that the potency of a novel bispyridinium oxime K203 to counteract sarin-induced neurotoxicity is relatively low and roughly corresponds to the neuroprotective efficacy of obidoxime. Among tested oximes, the oxime HI-6 seems to be significanlty more efficacious to counteract acute neurotoxicity of sarin than commonly used obidoxime and a newly developed oxime K203. Thus, the oxime K203 does not provide any beneficial effect for the antidotal treatment of acute poisoning with sarin in comparison with the oxime HI-6 that should be considered to be the best oxime for antidotal treatment of acute sarin poisonings.
  • The neuroprotective effects of a newly developed oxime K203 and currently available oximes (obidoxime, HI-6) in combination with atropine in rats poisoned with sarin were studied. The sarin-induced neurotoxicity was monitored using a functional observatory battery at 2 similar to hr after sarin challenge. The results indicate that the potency of a novel bispyridinium oxime K203 to counteract sarin-induced neurotoxicity is relatively low and roughly corresponds to the neuroprotective efficacy of obidoxime. Among tested oximes, the oxime HI-6 seems to be significanlty more efficacious to counteract acute neurotoxicity of sarin than commonly used obidoxime and a newly developed oxime K203. Thus, the oxime K203 does not provide any beneficial effect for the antidotal treatment of acute poisoning with sarin in comparison with the oxime HI-6 that should be considered to be the best oxime for antidotal treatment of acute sarin poisonings. (en)
Title
  • A comparison of the potency of a novel bispyridinium oxime K203 and currently available oximes (obidoxime, HI-6) to counteract the acute neurotoxicity of sarin in rats
  • A comparison of the potency of a novel bispyridinium oxime K203 and currently available oximes (obidoxime, HI-6) to counteract the acute neurotoxicity of sarin in rats (en)
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  • A comparison of the potency of a novel bispyridinium oxime K203 and currently available oximes (obidoxime, HI-6) to counteract the acute neurotoxicity of sarin in rats
  • A comparison of the potency of a novel bispyridinium oxime K203 and currently available oximes (obidoxime, HI-6) to counteract the acute neurotoxicity of sarin in rats (en)
skos:notation
  • RIV/60162694:G44__/12:43874582!RIV13-MO0-G44_____
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  • 120103
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  • RIV/60162694:G44__/12:43874582
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  • MICE; BLOOD; ACETYLCHOLINESTERASE; BRAIN; NERVE AGENTS; PYRIDINIUM OXIMES; ANTIDOTAL TREATMENT; ORGANOPHOSPHORUS COMPOUNDS; NEUROPROTECTIVE EFFICACY; TABUN-POISONED RATS (en)
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  • US - Spojené státy americké
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  • [9392398BC732]
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  • Basic & Clinical Pharmacology & Toxicology
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  • 111
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  • Kassa, Jiří
  • Misík, Jan
  • Žďárová Karasová, Jana
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  • 000309921600007
issn
  • 1742-7835
number of pages
http://bibframe.org/vocab/doi
  • 10.1111/j.1742-7843.2012.00897.x
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  • G44
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