
HI-6 and TMB-4 were the most effective and safe of 7 cholinesterase reactivators tested as agents for the prophylaxis of proserine poisoning of male mice. The reactivator HI-6 strongly potentiated the prophylactic efficacy of a mixture of atropine and arpenal administered in the doses sufficient for the blockade of both the m- and h-cholinoreactive systems of mice. As demonstrated by experiments in vitro, HI-6 and TMB-4 did not reacivate proserine-inhibited cholinesterase. The natural anticholinesterase activity of HI-6 was negligible. Based on the correlation of the data obtained to the reported data indicating that HI-6 has a low ganglioblocking activity it is inferred that the direct effect on the receptor is of no importance for the potentiating effect. It is assumed that HI-6 modulates the cholinoreactive systems, which leads to a dramatic increase of the efficacy of cholinolytics.
Atropine, Male, Cholinesterase Reactivators, Obidoxime Chloride, Pralidoxime Compounds, Antidotes, Parasympatholytics, Drug Synergism, Pyridinium Compounds, Butanones, Neostigmine, Mice, Oximes, Animals, Trimedoxime, Diphenylacetic Acids
Atropine, Male, Cholinesterase Reactivators, Obidoxime Chloride, Pralidoxime Compounds, Antidotes, Parasympatholytics, Drug Synergism, Pyridinium Compounds, Butanones, Neostigmine, Mice, Oximes, Animals, Trimedoxime, Diphenylacetic Acids
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