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[大鼠急性中毒期间所选抗胆碱能药物对GV物质胆碱能和非胆碱能作用影响的比较]

[Comparison of the effect of selected anticholinergic agents on cholinergic and noncholinergic effects of GV substances during acute poisoning in rats].

作者信息

Kassa J, Bajgar J

机构信息

Vojenská lékarská akademie JEP, Hradec Králové.

出版信息

Ceska Slov Farm. 1994 Oct;43(5):222-5.

PMID:7982005
Abstract

In experiments on male rats, the effect of selected cholinolytic agents (atropine, benactyzine, G 3063) in combination with the reactivator of cholinesterases HI-6 on the cholinergic and non-cholinergic effects of GV substance in the course of acute sublethal intoxication was compared. The cholinergic affects of GV substance were examined by means of the changes in the activity of cholinesterases in whole blood, the CNS, diaphragm and liver, the noncholinergic stressogenic effects by means of the changes in the level of corticosterone in plasma and the activity of tyrosine amino transferase in the liver. It follows from the changes in the activity of cholinesterases that the cholinergic effects of GV substance are least influenced by atropine, whereas benactyzine and G 3063 exert an approximately similar effect. The difference in the effect is evident especially in the 24th hour of intoxication. Similarly stressogenic effects of GV substance are least influenced by an antidotal combination of atropine and HI-6. It means that the centrally acting cholinolytic agents benactyzine and G 3063 are more advantageous for the therapy of GV substance poisonings than the peripherally acting atropine.

摘要

在对雄性大鼠进行的实验中,比较了选定的胆碱能解抗剂(阿托品、苯那辛、G 3063)与胆碱酯酶复活剂HI-6联合使用时,对急性亚致死性中毒过程中GV物质的胆碱能和非胆碱能效应的影响。通过全血、中枢神经系统、膈肌和肝脏中胆碱酯酶活性的变化来检测GV物质的胆碱能效应,通过血浆中皮质酮水平的变化和肝脏中酪氨酸氨基转移酶的活性来检测非胆碱能应激效应。从胆碱酯酶活性的变化可以看出,阿托品对GV物质的胆碱能效应影响最小,而苯那辛和G 3063的作用大致相似。这种效应差异在中毒后第24小时尤为明显。同样,阿托品和HI-6的解毒组合对GV物质的应激效应影响最小。这意味着,与外周作用的阿托品相比,中枢作用的胆碱能解抗剂苯那辛和G 3063在治疗GV物质中毒方面更具优势。

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