Cole S O
Psychology Department, Rutgers University, Camden, NJ 08102.
Psychopharmacology (Berl). 1988;96(4):458-61. doi: 10.1007/BF02180024.
Chlordiazepoxide (10 mg/kg), administered on eight successive acquisition sessions, impaired a light-cued, successive discrimination in male Sprague-Dawley rats by increasing the number of incorrect responses. The benzodiazepine receptor antagonist Ro 15-1788 (5 and 10 mg/kg) reversed the discrimination impairment and reduced the number of incorrect responses in a generally dose-dependent manner when co-administered with chlordiazepoxide. These findings suggest that the impairment of successive discrimination by chlordiazepoxide is mediated by central benzodiazepine receptor sites. When administered alone, however, the 10 mg/kg dose of Ro 15-1788 (but not the 5 mg/kg dose) produced a mild benzodiazepine-like impairment in discrimination, which was accompanied by a small but significant increase in incorrect responses. These findings suggest that Ro 15-1788 may also have some intrinsic action of its own, which needs to be assessed independently of its use as a mediational research tool.
在连续八个习得训练阶段给予氯氮卓(10毫克/千克),会增加雄性斯普拉格-道利大鼠的错误反应次数,从而损害其对光刺激的连续辨别能力。苯二氮卓受体拮抗剂Ro 15-1788(5毫克/千克和10毫克/千克)与氯氮卓共同给药时,能逆转辨别能力损害,并以一般剂量依赖性方式减少错误反应次数。这些发现表明,氯氮卓对连续辨别能力的损害是由中枢苯二氮卓受体位点介导的。然而,单独给予10毫克/千克剂量的Ro 15-1788(而非5毫克/千克剂量)会产生轻微的苯二氮卓样辨别能力损害,同时错误反应次数有小幅但显著的增加。这些发现表明,Ro 15-1788可能也有其自身的一些内在作用,需要独立于其作为中介研究工具的用途进行评估。