Koplovitz I, Menton R, Matthews C, Shutz M, Nalls C, Kelly S
U.S. Army Medical Research Institute of Chemical Defense, Aberdeen Proving Ground, MD 21010, USA.
Drug Chem Toxicol. 1995 May-Aug;18(2-3):119-36. doi: 10.3109/01480549509014316.
HI-6 (1-2-hydroxyiminomethyl-1-pyridino-3-(4-carbamoyl-1-pyridino -2- oxapropane dichloride) has been evaluated as an oxime alternative to pralidoxime, and toxogonin in the treatment of organophosphorus (OP) poisoning. The dose response effects of atropine (ATR) and HI-6 were investigated to more fully explore the interaction of these compounds in the treatment of OP poisoning. ATR, HI-6 and various combinations of the two drugs were evaluated against lethal poisoning by soman (GD) and tabun (GA) in guinea pigs. The effect of adjunctive diazepam treatment on the efficacy of atropine and HI-6 against soman was also investigated. Animals of either sex were challenged s.c. with OP and treated i.m. 1 min later with ATR and/or HI-6. When used, diazepam was injected immediately after ATR+HI6. LD50s of each treatment were calculated from probit models based on 24-hour survival against 5 levels of nerve agent and 6 animals per challenge level. A protective index (PI) was calculated by dividing the nerve agent LD50 in the presence of treatment by the LD50 in the absence of treatment. Treatment with HI6 alone had little effect on the toxicity of either OP. Treatment with ATR alone was more effective than HI-6 alone and was significantly more effective against soman than against tabun. When used in combination atropine and HI-6 had a strong synergistic effect against both agents. The dose of atropine used with HI-6 was critical in determining the efficacy of HI-6 against either agent. The slopes of the dose-lethality curves were minimally affected by the dose of ATR or HI-6. Adjunctive treatment with diazepam enhanced the efficacy of HI-6 and atropine against soman. It is concluded that 1) ATR has a large effect on the efficacy of HI-6 against OP poisoning, 2) the dose of ATR must be carefully selected in studies investigating the efficacy of HI-6 against OP poisoning, 3) the effective dose of ATR in the guinea pig is approximately 16 mg/kg, and 4) diazepam is a useful adjunct to atropine and HI-6.
己二肟(1-2-羟基亚氨基甲基-1-吡啶基-3-(4-氨基甲酰基-1-吡啶基-2-氧杂丙烷二氯化物))已被评估为用于治疗有机磷(OP)中毒的解磷定和双复磷的肟替代物。研究了阿托品(ATR)和己二肟的剂量反应效应,以更全面地探究这些化合物在治疗OP中毒中的相互作用。评估了ATR、己二肟以及两种药物的各种组合对豚鼠中梭曼(GD)和塔崩(GA)致死性中毒的作用。还研究了辅助使用地西泮治疗对ATR和己二肟抗梭曼疗效的影响。对不同性别的动物皮下注射OP,并在1分钟后肌肉注射ATR和/或己二肟。若使用地西泮,则在ATR+己二肟之后立即注射。根据基于24小时存活率针对5个神经毒剂水平且每个挑战水平6只动物的概率模型计算每种治疗的半数致死剂量(LD50)。通过将治疗存在时的神经毒剂LD50除以无治疗时的LD50来计算保护指数(PI)。单独使用己二肟治疗对两种OP的毒性几乎没有影响。单独使用ATR治疗比单独使用己二肟更有效,且对梭曼的疗效比对塔崩显著更有效。当联合使用时,阿托品和己二肟对两种毒剂均有强烈的协同作用。与己二肟一起使用的阿托品剂量对于确定己二肟对任何一种毒剂的疗效至关重要。剂量-致死率曲线的斜率受ATR或己二肟剂量的影响最小。辅助使用地西泮可增强己二肟和阿托品抗梭曼的疗效。得出以下结论:1)ATR对己二肟治疗OP中毒的疗效有很大影响;2)在研究己二肟治疗OP中毒的疗效时,必须仔细选择ATR的剂量;3)豚鼠中ATR的有效剂量约为16mg/kg;4)地西泮是阿托品和己二肟的有用辅助药物。