Protective Effect of Combinational Antidotes Composed of Physostigmine and Procyclidine Against Nerve-agent Poisoning

  • Kim, Yun-Bae (Biomedical Assessment Laboratory (GSDC-2-4), Agency for Defense Development) ;
  • Cheon, Ki-Cheol (Biomedical Assessment Laboratory (GSDC-2-4), Agency for Defense Development) ;
  • Hur, Gyeung-Haeng (Biomedical Assessment Laboratory (GSDC-2-4), Agency for Defense Development) ;
  • Phi, Taek-San (Biomedical Assessment Laboratory (GSDC-2-4), Agency for Defense Development) ;
  • Kim, Jee-Cheon (Biomedical Assessment Laboratory (GSDC-2-4), Agency for Defense Development) ;
  • Deasik Hang (Biomedical Assessment Laboratory (GSDC-2-4), Agency for Defense Development)
  • Published : 2000.09.01

Abstract

Antidotal efficacy of physostigmine plus procyclidine, the combinational prophylactics for organophosphate poisoning, was evaluated in rats and guinea pigs. To assess the dose-response relation-ship in rats, various doses (0.3-6.0mg/kg) of procyclidine in combination with a fixed dose (0.1mg/kg) of physostigmine were pretreated subcutaneously 30 min prior to subcutaneous exposure to nerve-agents. Physostigmine alone exerted protection ratios of 2.44, 1.20, 1.50, 1.50 and 2.20 folds for tabun, sarin, soman, cyclosarin and V-agent, respectively. Interestingly, coadmnistration of procyclidine with physostigmine exhibited remarkable synergistic effects in a dose-dependent manner, leading to 4.00~8.00 folds for tabun, 2.15-8.50 folds for sarin, 1.92~507 folds for so man, 2.15~2.90 folds for cyclosarin, and 2.71~10.50 folds for V-agent. On the contrary, a low effect (l.65 fold) was achieved with the traditional antidotes atropine (17.4 mg/kg) plus 2-pralidoxime (30 mg/kg) treated immediately after soman poisoning. Noteworthy, the combinational prophylactics markedly potentiated the effect of atropine plus 2-pralidoxime to 6.13 and 12.27 folds with 1.0 and 3.0 mg/kg of procyclidine, respectively, against soman poisoning. In guinea pigs, the physostigmine plus procyclidine prophylactics exerted protective effects of 3.00~4.70 folds against soman intoxcation, which were much higher at low doses (0.3~1.0 mg/kg) of procyclidine than those in rats. Taken together, it is proposed that the combinational prophylactics composed oj physostigmine and procyclidine could be a promising antidote regimen for the poisoning with organophosphates possessing diverse properties.

Keywords