Petkov V V, Vuglenova Y
Acta Physiol Pharmacol Bulg. 1985;11(3):37-43.
In training for passive avoidance using a device of the step-down type, the nootropic agents piracetam (60 mg/kg orally) and centrophenoxine (100 mg/kg, i. p.) do not facilitate learning, while the ergot alkaloid elymoclavine (1 mg/kg, i. p.) tends to have a positive effect on learning and memory. The muscarine cholinergic receptor blocker scopolamine (2 mg/kg, i. p.) substantially deteriorates short-term memory in passive avoidance training. Piracetam in a dose of 600 mg/kg does not change the negative effect of scopolamine on the memory, while centrophenoxine (100 mg/kg) and elymoclavine (1 mg/kg) eliminate it in view of the fact that the impairment of the short-term memory in the reported experiments was induced by the cholinolytic agent scopolamine, it should be assumed that the observed effects of piracetam, centrophenoxine and elymoclavine are due to definite interactions between the cerebral cholinergic and monoaminergic mechanisms.
在使用逐步下降型装置进行被动回避训练时,促智药吡拉西坦(口服60毫克/千克)和盐酸甲氯芬酯(腹腔注射100毫克/千克)无助于学习,而麦角生物碱麦角隐亭(腹腔注射1毫克/千克)往往对学习和记忆有积极作用。毒蕈碱胆碱能受体阻滞剂东莨菪碱(腹腔注射2毫克/千克)在被动回避训练中会严重损害短期记忆。600毫克/千克剂量的吡拉西坦不会改变东莨菪碱对记忆的负面影响,而盐酸甲氯芬酯(100毫克/千克)和麦角隐亭(1毫克/千克)则消除了这种影响。鉴于所报道实验中短期记忆的损害是由胆碱能阻断剂东莨菪碱引起的,应该假定吡拉西坦、盐酸甲氯芬酯和麦角隐亭的观察到的效果是由于大脑胆碱能和单胺能机制之间的特定相互作用。