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A comparison of the efficacy of newly developed reversible inhibitors of acetylcholinesterase with commonly used pyridostigmine as pharmacological pre-treatment of soman-poisoned mice
J. Kassa, K. Musilek, M. Koomlova, J. Bajgar
Jazyk angličtina Země Dánsko
Typ dokumentu srovnávací studie, časopisecké články, práce podpořená grantem
NLK
Medline Complete (EBSCOhost)
od 2004-01-01 do Před 1 rokem
Wiley Online Library (archiv)
od 1997-01-01 do 2012-12-31
- MeSH
- antidota aplikace a dávkování farmakologie MeSH
- atropin aplikace a dávkování farmakologie MeSH
- chemické bojové látky otrava MeSH
- cholinesterasové inhibitory aplikace a dávkování farmakologie MeSH
- isochinoliny aplikace a dávkování farmakologie MeSH
- kombinovaná farmakoterapie MeSH
- LD50 MeSH
- myši MeSH
- oximy aplikace a dávkování farmakologie MeSH
- pyridinové sloučeniny aplikace a dávkování farmakologie MeSH
- pyridostigmin-bromid aplikace a dávkování farmakologie MeSH
- reaktivátory cholinesterázy aplikace a dávkování farmakologie MeSH
- soman aplikace a dávkování otrava MeSH
- zvířata MeSH
- Check Tag
- mužské pohlaví MeSH
- myši MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- srovnávací studie MeSH
The ability of three newly developed reversible inhibitors of acetylcholinesterase (AChE) (K298, K344 and K474) and currently available carbamate pyridostigmine to increase the resistance of mice against soman and the efficacy of antidotal treatment of soman-poisoned mice was compared. Neither pyridostigmine nor new reversible inhibitors of AChE were able to increase the LD(50) value of soman. Thus, the pharmacological pre-treatment with pyridostigmine or newly synthesized inhibitors of AChE was not able to protect mice against soman-induced lethal acute toxicity. The pharmacological pre-treatment with pyridostigmine alone or with K474 was able to slightly increase the efficacy of antidotal treatment (the oxime HI-6 in combination with atropine) of soman-poisoned mice, but the increase in the efficacy of antidotal treatment was not significant. The other newly developed reversible inhibitors of AChF (K298, K344) were completely ineffective. These findings demonstrate that pharmacological pre-treatment of soman-poisoned mice with tested reversible inhibitors of AChF is not promising.
Citace poskytuje Crossref.org
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