Effect of seven newly synthesized and currently available oxime cholinesterase reactivators on cyclosarin-intoxicated rats
Jazyk angličtina Země Švýcarsko Médium electronic
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
19742125
PubMed Central
PMC2738912
DOI
10.3390/ijms10073065
PII: i10073065
Knihovny.cz E-zdroje
- Klíčová slova
- acetylcholinesterase, butyrylcholinesterase, cyclosarin, oximes, reactivators,
- MeSH
- acetylcholinesterasa krev metabolismus MeSH
- atropin farmakologie MeSH
- krysa rodu Rattus MeSH
- mozek účinky léků enzymologie MeSH
- organofosforové sloučeniny toxicita MeSH
- oximy chemie farmakologie MeSH
- potkani Wistar MeSH
- reaktivátory cholinesterázy chemie farmakologie MeSH
- vztah mezi dávkou a účinkem léčiva MeSH
- zvířata MeSH
- Check Tag
- krysa rodu Rattus MeSH
- mužské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- acetylcholinesterasa MeSH
- atropin MeSH
- cyclohexyl methylphosphonofluoridate MeSH Prohlížeč
- organofosforové sloučeniny MeSH
- oximy MeSH
- reaktivátory cholinesterázy MeSH
Seven new oxime-based acetylcholinesterase reactivators were compared with three currently available ones (obidoxime, trimedoxime, HI-6) for their ability to lessen cholinesterase inhibition in blood and brain of cyclosarin-treated rats. Oximes were given at doses of 5% their LD(50) along with 21 mg/kg atropine five min before the LD(50) of cyclosarin (120 ug/kg) was administered. Blood and brain samples were collected 30 minutes later. The greatest difference between acetylcholinesterase inhibition in blood of cyclosarin-treated rats was found after administration of HI-6 (40%), compared to 22% for trimedoxime and 6% for obidoxime. Only two of the seven newly synthesized oximes had any effect (K203 at 7%, K156 at 5%). Effective oximes against cyclosarin-inhibited plasma butyrylcholinesterase were HI-6 (42%), trimedoxime (11%), and K156 (4%). The oximes were less effective in brain than in blood, with reactivation values for HI-6 30% against acetylcholinesterase and 10% against butyrylcholinesterase. Values for newly synthesized oximes were less than 10% for K206, K269 and K203.
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