Carli M, Ballabio M, Caccia S, Garattini S, Samanin R
Arzneimittelforschung. 1981;31(10):1721-3.
Brain distribution and various pharmacological effects of 7-nitro-2-amino-5-phenyl-1,5-benzodiazepine (CP 1414 S) and diazepam were studied in rats. Injected at 10 mg/kg i.p., the compounds reached brain peak concentrations 15 min after administration and showed an apparent half-life of about 50 min. CP 1414 S was about ten times less potent than diazepam in protecting rats from pentetrazole convulsions, increasing punished responses in a "conflict" test and disrupting rotarod performance. At the lowest doses effective in these tests diazepam, but not CP 1414 S, caused significant reduction of spontaneous locomotor activity in rats. On the basis of the test selected, it is concluded that CP 1414 S causes effects similar to those shown by diazepam in the same conditions, although with less potency. It causes less depression of motor behaviour than diazepam, at least at the lowest doses and in rats.
研究了7-硝基-2-氨基-5-苯基-1,5-苯并二氮杂䓬(CP 1414 S)和地西泮在大鼠体内的脑部分布及各种药理作用。以10 mg/kg腹腔注射给药后,这些化合物在给药15分钟后达到脑内峰值浓度,表观半衰期约为50分钟。在保护大鼠免受戊四氮惊厥、增加“冲突”试验中的惩罚反应以及破坏旋转棒性能方面,CP 1414 S的效力约为地西泮的十分之一。在这些试验中有效最低剂量下,地西泮会导致大鼠自发运动活动显著减少,但CP 1414 S不会。根据所选试验得出结论,CP 1414 S在相同条件下产生的作用与地西泮相似,尽管效力较低。至少在最低剂量下且在大鼠中,它对运动行为的抑制作用比地西泮小。