The influence of modulators of acetylcholinesterase on the resistance of mice against soman and on the effectiveness of antidotal treatment of soman poisoning in mice

被引:7
|
作者
Kassa, Jiri [1 ]
Korabecny, Jan [1 ]
Nepovimova, Eugenie [1 ]
Jun, Daniel [1 ]
机构
[1] Univ Def Brno, Fac Mil Hlth Sci, Dept Toxicol & Mil Pharm, Hradec Kralove, Czech Republic
关键词
Soman; 6-Chlorotacrine; K027; Atropine; HI-6; Mice; ORGANOPHOSPHORUS NERVE AGENTS; CHEMICAL WARFARE AGENTS; IN-VITRO; PHARMACOLOGICAL PROPHYLAXIS; PYRIDINIUM OXIMES; EFFICACY; REACTIVATION; PYRIDOSTIGMINE; BRAIN; RATS;
D O I
10.1016/j.jab.2017.01.004
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
The potency of one reversible inhibitor of acetylcholinesterase (6-chlorotacrine), one reactivator of acetycholinesterase (K027) and their combination to increase the resistance of mice against soman and the efficacy of antidotal treatment of soman-poisoned mice was evaluated. While 6-chlorotacrine was able to markedly protect mice against acute toxicity of soman and the pharmacological pretreatment with 6-chlorotacrine increased the efficacy of antidotal treatment (the oxime HI-6 in combination with atropine) of soman-poisoned mice more than two times, the bispyridinium oxime K027 did not protect mice from acute toxicity of soman, however, the pharmacological pretreatment with this compound was able to markedly increase the efficacy of antidotal treatment of soman-poisoned mice. On the other hand, the combination of both modulators of acetylcholinesterase did not increase the prophylactic efficacy of 6-chlorotacrine alone. These findings demonstrate that pharmacological pretreatment of soman-poisoned mice can be promising and useful in the case of administration of 6-chlorotacrine while the administration of the oxime K027 did not bring any additional benefit when combined with 6-chlorotacrine. (C) 2017 Published by Elsevier Sp. z o.o. on behalf of Faculty of Health and Social Sciences, University of South Bohemia in Ceske Budejovice.
引用
收藏
页码:10 / 14
页数:5
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