Geller I, Hartmann R J
J Clin Psychiatry. 1982 Dec;43(12 Pt 2):25-33.
Rats trained on an avoidance-escape task were administered buspirone in doses ranging from 0.5 to 7.5 mg/kg. Low doses disrupted avoidance responding without impairing escape responding. Rats trained on an experimentally induced conflict procedure were also administered buspirone or diazepam (1.0 to 5.0 mg/kg). Buspirone and diazepam appeared to be equipotent as anxiolytics. Cynomolgus monkeys, also trained on the experimentally induced conflict task, were given intramuscular buspirone or diazepam (0.5 to 5.0 mg/kg). Both drugs produced an attentuation of conflict, further supporting the anxiolytic equipotency of buspirone and diazepam. The long duration of action of buspirone suggests the presence of at least one active metabolite.
对接受回避-逃避任务训练的大鼠给予剂量范围为0.5至7.5毫克/千克的丁螺环酮。低剂量会干扰回避反应而不损害逃避反应。对接受实验诱导冲突程序训练的大鼠也给予丁螺环酮或地西泮(1.0至5.0毫克/千克)。丁螺环酮和地西泮作为抗焦虑药似乎等效。对同样接受实验诱导冲突任务训练的食蟹猴给予肌肉注射丁螺环酮或地西泮(0.5至5.0毫克/千克)。两种药物均使冲突减弱,进一步支持了丁螺环酮和地西泮抗焦虑等效性。丁螺环酮作用持续时间长表明至少存在一种活性代谢物。