Sansone M, Battaglia M, Vetulani J
Istituto di Psicobiologia e Psicofarmacologia, CNR, Roma, Italy.
Pol J Pharmacol. 1995 Jan-Feb;47(1):69-73.
The tricyclic antidepressant desipramine impaired shuttle-box avoidance acquisition in mice of the CD-1 strain. The nootropic drug oxiracetam was unable to prevent the desipramine-induced learning impairment, while a protective action was exerted by minaprine, a psychotropic agent regarded as an atypical antidepressant drug, possessing dopaminergic and related memory-enhancing properties. It seems likely that the dopaminergic action of minaprine played a determinant role in its avoidance improving effects in desipramine treated mice, because similar effects were produced by amphetamine. However, in contrast to amphetamine, minaprine did not enhance locomotor activity and did not show signs of general behavioral stimulation.
三环类抗抑郁药地昔帕明损害了CD-1品系小鼠在穿梭箱实验中的回避反应习得。促智药奥拉西坦无法预防地昔帕明引起的学习障碍,而米那普明却发挥了保护作用。米那普明是一种被视为非典型抗抑郁药的精神药物,具有多巴胺能及相关的增强记忆特性。米那普明的多巴胺能作用似乎在其改善地昔帕明处理小鼠回避反应的效应中起了决定性作用,因为苯丙胺也产生了类似效应。然而,与苯丙胺不同的是,米那普明并未增强运动活性,也未表现出一般行为兴奋的迹象。