File S E, Dingemanse J, Friedman H L, Greenblatt D J
Psychopharmacology (Berl). 1986;89(1):113-7. doi: 10.1007/BF00175201.
Ro 15-1788 (flumazepil) is an imidazodiazepine that is able to antagonise most of the behavioural actions of the benzodiazepines, as well as having some intrinsic effects. Acute administration of Ro 15-1788 (10 mg/kg) decreases social interaction between male rats and elevates exploratory head-dipping. After 5 days of pretreatment there was tolerance to the former effect, although Ro 15-1788 retained its ability to antagonise the effects on social interaction of the beta-carboline, FG 7142. Ro 15-1788 also retained its ability to elevate head-dipping: additionally, the chronically-treated rats had elevated motor activity and rearing scores. The acute effects of lorazepam in the holeboard were unchanged by chronic pretreatment with Ro-15-1788. The plasma and brain concentrations after acute administration of lorazepam were unchanged following chronic administration of Ro 15-1788. After chronic treatment the brain concentrations of Ro 15-1788 were unchanged. It is unlikely that pharmacokinetic factors could underlie the different behavioural changes following chronic treatment.
Ro 15 - 1788(氟马西尼)是一种咪唑并二氮䓬类药物,它能够拮抗苯二氮䓬类药物的大多数行为效应,同时还具有一些内在效应。急性给予Ro 15 - 1788(10毫克/千克)会减少雄性大鼠之间的社交互动,并增加探索性探首行为。预处理5天后,对前一种效应产生了耐受性,尽管Ro 15 - 1788仍保留其拮抗β-咔啉FG 7142对社交互动影响的能力。Ro 15 - 1788还保留了增加探首行为的能力:此外,长期治疗的大鼠运动活动和竖毛评分升高。用Ro - 15 - 1788进行慢性预处理后,劳拉西泮在洞板实验中的急性效应未发生改变。长期给予Ro 15 - 1788后,急性给予劳拉西泮后的血浆和脑浓度未发生变化。长期治疗后,Ro 15 - 1788的脑浓度未发生变化。药代动力学因素不太可能是长期治疗后不同行为变化的基础。