
doi: 10.5507/bp.2005.073
pmid: 16601803
The present study was performed to assess and compare a therapeutic efficacy of obidoxime, HI-6, BI-6 and HS-6 administered in equimolar doses and combined with atropine in cyclosarin-poisoned mice and rats. It was demonstrated that all the therapeutic regimens tested, were able to decrease the cyclosarin-induced toxicity significantly - at least 1.5 times. Higher therapeutic ratios, almost three times, were achieved in rats in comparison with mice. The highest therapeutic ratio was achieved for therapeutic regimen consisting of HI-6 and atropine in both mice and rats. Obidoxime was the least effective oxime in the treatment of cyclosarin intoxication. The BI-6 oxime was significantly more efficacious than obidoxime (in both mice and rats) and HS-6 (in rats) but its effectiveness did not reach the efficacy of HI-6.
Cholinesterase Reactivators, Obidoxime Chloride, Pralidoxime Compounds, Pyridinium Compounds, Rats, Mice, Organophosphate Poisoning, Organophosphorus Compounds, Oximes, Animals, Female
Cholinesterase Reactivators, Obidoxime Chloride, Pralidoxime Compounds, Pyridinium Compounds, Rats, Mice, Organophosphate Poisoning, Organophosphorus Compounds, Oximes, Animals, Female
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