Gozzani J L, Izquierdo I
Psychopharmacology (Berl). 1976 Aug 26;49(1):109-11. doi: 10.1007/BF00427480.
The posttrial i.p. administration of clonidine (0.1 mg/kg) or haloperidol (0.5 mg/kg) to rats trained on a shuttle avoidance paradigm resulted in lower retention of the task in a retest session carried out 7 days later, compared to animals which received posttrial saline injections. The effect of clonidine was antagonized by either phenoxybenzamine (10 mg/kg) or phentolamine (10 mg/kg) i.p., and that of haloperidol was antagonized by 4, but not by 0.5 mg/kg of apomorphine i.p. Neither apomorphine, nor phentolamine or phenoxybenzamine had any effect on their own. The data suggest that memory consolidation of two-way avoidance may be influenced by presumably peripheral adrenergic mechanisms and by presumably central dopaminergic mechanisms.
在穿梭箱回避范式训练的大鼠中,试验后腹腔注射可乐定(0.1毫克/千克)或氟哌啶醇(0.5毫克/千克),与试验后接受生理盐水注射的动物相比,在7天后进行的复测中任务保留率较低。可乐定的作用可被腹腔注射的酚苄明(10毫克/千克)或酚妥拉明(10毫克/千克)拮抗,氟哌啶醇的作用可被4毫克/千克而非0.5毫克/千克的腹腔注射阿扑吗啡拮抗。阿扑吗啡、酚妥拉明或酚苄明单独使用均无任何作用。数据表明,双向回避的记忆巩固可能受到推测的外周肾上腺素能机制和推测的中枢多巴胺能机制的影响。