Doherty T J, Ballinger J A, McDonell W N, Pascoe P J, Valliant A E
Can J Vet Res. 1987 Apr;51(2):244-8.
Idazoxan was studied at three dose rates to assess its potential as an antagonist to xylazine. Calves in the study group were initially given xylazine at a dose rate of 0.2 mg/kg intravenously followed 12 minutes later by idazoxan at a dose rate of either 0.05, 0.075 or 0.10 mg/kg intravenously. A control group received a saline injection instead of idazoxan. All three dose levels of idazoxan successfully reversed the xylazine induced central nervous depression and all animals stood within two minutes of injection. No residual signs of sedation were noticed and relapse did not occur. In addition idazoxan was successful in reversing respiratory and cardiovascular depression produced by xylazine. The results indicated that idazoxan may be used for rapid reversal of xylazine induced sedation in calves.
研究了咪唑克生在三种剂量率下作为赛拉嗪拮抗剂的潜力。研究组的犊牛最初静脉注射剂量率为0.2mg/kg的赛拉嗪,12分钟后静脉注射剂量率分别为0.05、0.075或0.10mg/kg的咪唑克生。对照组接受生理盐水注射而非咪唑克生。咪唑克生的所有三个剂量水平均成功逆转了赛拉嗪引起的中枢神经抑制,所有动物在注射后两分钟内站立。未观察到残留的镇静迹象,也未发生复发。此外,咪唑克生还成功逆转了赛拉嗪引起的呼吸和心血管抑制。结果表明,咪唑克生可用于快速逆转犊牛由赛拉嗪引起的镇静作用。