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与中枢神经系统抑制剂相比,丁螺环酮在大鼠中的辨别性刺激特性。

Discriminative stimulus properties of buspirone compared to central nervous system depressants in rats.

作者信息

Hendry J S, Balster R L, Rosecrans J A

出版信息

Pharmacol Biochem Behav. 1983 Jul;19(1):97-101. doi: 10.1016/0091-3057(83)90317-9.

Abstract

Two groups of rats were trained to discriminate either IP buspirone from vehicle or IP oxazepam from vehicle using a two-lever FR-10 schedule of sweetened milk presentation. The discrimination in the buspirone group was difficult to establish due to potent response rate decreasing effects. Oxazepam was a very effective stimulus and the discrimination in the oxazepam group was readily established. Tests with oxazepam and pentobarbital in the buspirone group provided no evidence for generalization of the stimulus properties of buspirone to either drug. Tests with buspirone in the oxazepam group also provided no evidence of generalization to buspirone, although tests with pentobarbital indicated almost complete generalization. Finally buspirone and oxazepam were tested in a group of rats previously trained to discriminate pentobarbital from vehicle. The findings supported the data obtained in the buspirone and oxazepam groups, with no indication of generalization from pentobarbital to buspirone, but with complete generalization to oxazepam. These data suggest that buspirone does not share discriminative stimulus properties which are common to other CNS depressants.

摘要

将两组大鼠训练至使用加糖牛奶呈现的双杠杆固定比率10程序来区分腹腔注射的丁螺环酮与赋形剂,或者区分腹腔注射的奥沙西泮与赋形剂。由于丁螺环酮组存在显著的反应率降低效应,因此很难建立起辨别能力。奥沙西泮是一种非常有效的刺激物,奥沙西泮组的辨别能力很容易就建立起来了。在丁螺环酮组中用奥沙西泮和戊巴比妥进行测试,没有发现丁螺环酮的刺激特性向这两种药物中的任何一种泛化的证据。在奥沙西泮组中用丁螺环酮进行测试,也没有发现向丁螺环酮泛化的证据,尽管用戊巴比妥进行测试表明几乎完全泛化。最后,在一组先前训练至区分戊巴比妥与赋形剂的大鼠中对丁螺环酮和奥沙西泮进行测试。这些发现支持了在丁螺环酮组和奥沙西泮组中获得的数据,没有迹象表明从戊巴比妥向丁螺环酮泛化,但向奥沙西泮完全泛化。这些数据表明,丁螺环酮不具有其他中枢神经系统抑制剂共有的辨别刺激特性。

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