Kuribara H, Tadokoro S
Division of Behavior Analysis, Gunma University School of Medicine, Maebashi, Japan.
Nihon Yakurigaku Zasshi. 1989 Apr;93(4):245-53. doi: 10.1254/fpj.93.245.
Single administration of NC-1100 (3, 10 or 30 mg/kg, p.o.) produced no marked change in the ambulatory activity and discrete lever-press avoidance response. However, 100 mg/kg of this drug produced a toxic effect which was characterized by salivation, tremor, clonic convulsion, etc., but none of the mice died. NC-1100 enhanced the ambulation-increasing effect of methamphetamine (2 mg/kg, s.c.) at 3 and 10 mg/kg, while it failed to modify that of scopolamine (0.5 mg/kg, s.c.). NC-1100, at 100 mg/kg, suppressed both the established discrete lever-press and shuttle avoidance responses, probably due to non-specific and toxic effects. When NC-1100 at 10 mg/kg was administered, the response rate increased only in the shuttle avoidance situation in which the avoidance established mice were used. Furthermore, when NC-1100 at 30 mg/kg was administered immediately before the start of the training session, the avoidance rate increased. However, there was no marked change in the avoidance rate in the 2nd training session which was conducted 24 hr after the 1st training session without the drug administration. Additionally, the response rate increased in the 1st and 2nd training sessions after 10 and 30 mg/kg of NC-1100. The present results suggest that NC-1100 may show a behavior-facilitating effect, although its effect is mild and different from that of typical central stimulants such as methamphetamine.
单次口服给予NC - 1100(3、10或30毫克/千克)对活动能力和离散杠杆按压回避反应没有明显影响。然而,该药物100毫克/千克会产生毒性作用,表现为流涎、震颤、阵挛性惊厥等,但没有小鼠死亡。NC - 1100在3毫克/千克和10毫克/千克时增强了甲基苯丙胺(2毫克/千克,皮下注射)增加活动的作用,而对东莨菪碱(0.5毫克/千克,皮下注射)的作用没有影响。100毫克/千克的NC - 1100抑制了已建立的离散杠杆按压和穿梭回避反应,这可能是由于非特异性和毒性作用。当给予10毫克/千克的NC - 1100时,仅在使用已建立回避反应的小鼠的穿梭回避实验中反应率增加。此外,在训练开始前立即给予30毫克/千克的NC - 1100时,回避率增加。然而,在第一次训练后24小时进行的第二次训练中,在未给药的情况下回避率没有明显变化。另外,给予10毫克/千克和30毫克/千克的NC - 1100后,第一次和第二次训练中的反应率均增加。目前的结果表明,NC - 1100可能具有行为促进作用,尽管其作用轻微且与甲基苯丙胺等典型中枢兴奋剂不同。