File S E, Andrews N
Psychopharmacology Research Unit, UMDS Division of Pharmacology, Guy's Hospital, London, UK.
Eur J Pharmacol. 1993 Jun 11;237(1):127-30. doi: 10.1016/0014-2999(93)90101-m.
The effects of a low (0.001 mg/kg) and a high (0.1 mg/kg) dose of the R(+) and S(-) enantiomers of zacopride were investigated in the elevated plus-maze in control-treated and diazepam-withdrawn rats. The rats withdrawn from diazepam were tested 36 h after the last of 28 days of treatment (2 mg/kg per day). The rats withdrawn from diazepam had a significant anxiogenic response, shown by decreases in the percentage of open arm entries and the percentage of time spent on the open arms. The low dose of S(-)-zacopride and both doses of R(+)-zacopride significantly reversed this anxiogenic response. In contrast, in the control-treated rats there were no significant effects on any measure of either isomer at doses of 0.001, 0.1 or 1 mg/kg.
在对照处理的大鼠和撤掉地西泮的大鼠中,于高架十字迷宫中研究了低剂量(0.001 mg/kg)和高剂量(0.1 mg/kg)的扎考必利R(+)和S(-)对映体的作用。撤掉地西泮的大鼠在为期28天的治疗(每天2 mg/kg)结束后36小时接受测试。撤掉地西泮的大鼠出现了明显的致焦虑反应,表现为进入开放臂的百分比和在开放臂上花费时间的百分比降低。低剂量的S(-)-扎考必利和两种剂量的R(+)-扎考必利均显著逆转了这种致焦虑反应。相比之下,在对照处理的大鼠中,0.001、0.1或1 mg/kg剂量的任何一种异构体对任何测量指标均无显著影响。