Zimakova I E, Baĭchurina A Z, Zimakov Iu A
Farmakol Toksikol. 1987 Jan-Feb;50(1):8-10.
It was shown in experiments on mice that inhibition of the exploratory activity by ftoracizin, phenazepam, scopolamine hydrobromide and their combinations predominates in comparison with muscle relaxation. Phenazepam administered at the low dose (0.025 mg/kg) by its depressive effect on the central nervous system was an antagonist of ftoracizin and a synergist of scopolamine. Ftoracizin and scopolamine show a mutual dose-effects-dependent antagonism in the inhibitory action and acute toxicity (LD50).
在对小鼠的实验中发现,与肌肉松弛相比,氟尿嘧啶、苯那西泮、氢溴酸东莨菪碱及其组合对探索活动的抑制作用占主导。低剂量(0.025毫克/千克)的苯那西泮因其对中枢神经系统的抑制作用,是氟尿嘧啶的拮抗剂和东莨菪碱的协同剂。氟尿嘧啶和东莨菪碱在抑制作用和急性毒性(半数致死量)方面表现出相互的剂量效应依赖性拮抗作用。