Neural Systems and Plasticity Research Group, Department of Psychology, University of Saskatchewan, Saskatoon, SK, Canada S7 N 5A5.
Neurobiol Learn Mem. 2010 Feb;93(2):261-7. doi: 10.1016/j.nlm.2009.10.006. Epub 2009 Oct 24.
The mechanisms underlying the complex effects of acute stress on memory are incompletely understood. Previous work suggests that the activation of N-methyl-d-aspartate (NMDA) receptors specifically containing GluN2B subunits may underlie the disruptions in spatial memory retrieval caused by acute stress (Wong et al., 2007 PNAS 104:11471). The present experiments were designed to assess whether a similar mechanism is involved in recognition memory. Recognition memory retrieval was assessed in Sprague-Dawley rats using an object recognition test and an object-place recognition test, both of which rely on patterns of spontaneous exploration. Exposure to acute stress for 30 min immediately before the test phase of either test disrupted memory retrieval. Administration of the GluN2B-selective antagonist Ro25-6981 (6 mg/kg; i.p.) enhanced memory in the object recognition test regardless of whether animals were exposed to acute stress. In the object-place test, Ro25-6981 had no effect on memory retrieval in the absence of stress but promoted memory following acute stress. These data highlight the specific contributions made by GluN2B-containing NMDA receptors to recognition memory for different types of stimuli.
急性应激对记忆的复杂影响的机制尚不完全清楚。先前的工作表明,N-甲基-D-天冬氨酸(NMDA)受体的特异性激活,特别是包含 GluN2B 亚基的 NMDA 受体的激活,可能是急性应激引起的空间记忆检索障碍的基础(Wong 等人,2007 年 PNAS 104:11471)。本实验旨在评估类似的机制是否参与识别记忆。使用物体识别测试和物体位置识别测试评估 Sprague-Dawley 大鼠的识别记忆检索,这两种测试都依赖于自发探索模式。在测试阶段之前,急性应激暴露 30 分钟会破坏记忆检索。无论动物是否暴露于急性应激,给予 GluN2B 选择性拮抗剂 Ro25-6981(6mg/kg;腹腔注射)均可增强物体识别测试中的记忆。在物体位置测试中,Ro25-6981 在没有应激的情况下对记忆检索没有影响,但在急性应激后促进了记忆。这些数据突出了包含 GluN2B 的 NMDA 受体对不同类型刺激的识别记忆的特定贡献。