Jagdev N, Barar F S
Indian J Physiol Pharmacol. 1982 Jul-Sep;26(3):201-6.
Rats received a single training trial on an inhibitory avoidance (passive avoidance) task and retention trials 24 hr (R-I) and 48 hr (R-II) later, in a special two-chambered apparatus, and the mean step-through latency was determined. The animals were given the drug, either pre-trial, pre-trial plus pre-retention, pre-retention or post-trial. Physostigmine (0.1 mg/kg, ip) and atropine (6.0 mg/kg, ip) had no effect on learning, but they adversely affected retention, particularly at 24 hr. The effect seems to involve central cholinergic mechanisms of retention.
大鼠在一个特殊的双室装置中,于抑制性回避(被动回避)任务上接受单次训练试验,并在24小时(R-I)和48小时(R-II)后进行记忆保持试验,测定平均步穿潜伏期。在试验前、试验前加记忆保持前、记忆保持前或试验后给动物用药。毒扁豆碱(0.1毫克/千克,腹腔注射)和阿托品(6.0毫克/千克,腹腔注射)对学习没有影响,但它们对记忆保持有不利影响,尤其是在24小时时。这种影响似乎涉及记忆保持的中枢胆碱能机制。