Treatment of intoxication with GV compound in laboratory rats.

J Fusek, J Bajgar
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引用次数: 0

Abstract

Changes of some physiological functions in rats were studied following intoxication with new type of highly toxic organophosphate GV [2-dimethylaminoethyl-(dimethylamido)-fluorophosphate] in doses of 2x and 4x LD50 i.m. The intoxication has begun with increasing motoric activity followed by increased salivation, rumination and bristling. Tachypnoe and fasciculations followed by convulsions and death were observed later. Therapy of intoxication with GV compound (in dose of 2x LD50) in rats demonstrated the best antidotal effect of combination of benactyzine, atropine and HI-6. In GV intoxication in higher doses (4x LD50), therapeutic efficacy (survival of experimental animals) was limited for 24 hours. HI-6 can be therefore considered as potentially universal reactivator for the treatment of nerve agents intoxication.

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GV化合物治疗实验大鼠中毒。
研究了新型高毒性有机磷GV[2-二甲氨基乙基-(二甲氨基)氟磷酸]在2倍和4倍LD50剂量下中毒后大鼠某些生理功能的变化。中毒开始时运动活动增加,随后出现流涎、反刍和毛发增加。随后观察到心动过速和抽搐,随后出现抽搐和死亡。以2倍LD50剂量的GV化合物治疗大鼠中毒,苯那替嗪、阿托品和HI-6联用的解毒效果最好。在高剂量(4倍LD50)的GV中毒中,治疗效果(实验动物的生存)在24小时内受到限制。因此,HI-6可以被认为是治疗神经毒剂中毒的潜在通用再激活剂。
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