Panickar K S, McNaughton N
Department of Psychology, University of Otago, Dunedin, New Zealand.
Pharmacol Biochem Behav. 1991 Jun;39(2):275-8. doi: 10.1016/0091-3057(91)90179-6.
Buspirone is a novel anxiolytic which does not share the muscle relaxant, anticonvulsant and sedative properties of classical anxiolytics such as the benzodiazepines. It has variable effects in conflict tasks based on shock which normally show consistent effects with classical anxiolytics. The present experiment investigated the effects of buspirone on successive discrimination, a conflict task employing omission of reward rather than shock. Buspirone (3.3, 1.1 and 0.3 mg/kg, IP) and chlordiazepoxide (5 and 20 mg/kg, IP) were administered to separate groups of rats throughout acquisition of a visual successive discrimination. Chlordiazepoxide released nonrewarded responding in a dose-related fashion. The effects of buspirone were qualitatively similar in releasing response suppression but were both less in magnitude and less clearly related to dose. The experiment shows that the action of buspirone in successive discrimination tasks does not depend on the use of shock but, rather, appears to be a genuine failure to fully release behavioural inhibition.
丁螺环酮是一种新型抗焦虑药,它不具备经典抗焦虑药(如苯二氮䓬类药物)的肌肉松弛、抗惊厥和镇静特性。在基于电击的冲突任务中,丁螺环酮具有不同的作用,而经典抗焦虑药通常在这些任务中表现出一致的效果。本实验研究了丁螺环酮对连续辨别任务的影响,这是一种采用奖励缺失而非电击的冲突任务。在大鼠获取视觉连续辨别能力的整个过程中,将丁螺环酮(3.3、1.1和0.3毫克/千克,腹腔注射)和氯氮䓬(5和20毫克/千克,腹腔注射)分别给予不同组的大鼠。氯氮䓬以剂量相关的方式释放无奖励反应。丁螺环酮在释放反应抑制方面的作用在性质上相似,但程度较小且与剂量的关系不太明显。该实验表明,丁螺环酮在连续辨别任务中的作用不依赖于电击的使用,相反,似乎是真正未能完全释放行为抑制。