Santucci Anthony C, Cardiello Julia
Department of Psychology, Manhattanville College, Purchase, NY 10577, USA.
Behav Neurosci. 2004 Feb;118(1):248-52. doi: 10.1037/0735-7044.118.1.248.
The effect of various doses of the serotonin-1A agonist 8-OH-DPAT at training on 72-hr retention of passive avoidance was investigated in rats. Results indicated impaired retention, as measured by latency to avoid shock. However, when total time spent in the nonshock compartment at test was assessed, the performance of drug-treated subjects was not significantly different than that of control animals. It is suggested that although drug treatment produced initial retention impairment, the memory trace for the aversive event was reactivated (i.e., "reminder effect") when subjects entered the shock compartment at test. These data imply that pharmacological treatments, especially those that modulate serotonergic neurotransmission, that appear to disrupt learning per se may interrupt neural circuits involved in retrieval processes.
研究了在训练时给予大鼠不同剂量的5-羟色胺-1A激动剂8-羟基二丙胺基四氢萘(8-OH-DPAT)对被动回避反应72小时记忆保持的影响。结果表明,以避免电击的潜伏期来衡量,记忆保持受损。然而,当评估测试时在无电击隔室中花费的总时间时,药物处理组的表现与对照动物的表现没有显著差异。有人提出,虽然药物处理会导致最初的记忆保持受损,但当受试动物在测试时进入电击隔室时,厌恶事件的记忆痕迹会被重新激活(即“提醒效应”)。这些数据表明,那些似乎会破坏学习本身的药物治疗,尤其是那些调节5-羟色胺能神经传递的药物治疗,可能会中断参与提取过程的神经回路。