Department of Teaching and Training, Fourth Military Medical University, Xi'an, People's Republic of China.
PLoS One. 2009 Oct 26;4(10):e7548. doi: 10.1371/journal.pone.0007548.
In auditory fear conditioning, repeated presentation of the tone in the absence of shock leads to extinction of the acquired fear responses. The glutamate N-methyl-D-aspartate receptor (NMDAR) is thought to be involved in the extinction of the conditioned fear responses, but its detailed role in initiating and consolidating or maintaining the fear extinction memory is unclear. Here we investigated this issue by using a NMDAR antagonist, MK-801.
METHODS/MAIN FINDINGS: The effects of immediate (beginning at 10 min after the conditioning) and delayed (beginning at 24 h after conditioning) extinctions were first compared with the finding that delayed extinction caused a better and long-lasting (still significant on the 20(th) day after extinction) depression on the conditioned fear responses. In a second experiment, MK-801 was intraperitoneally (i.p.) injected at 40 min before, 4 h or 12 h after the delayed extinction, corresponding to critical time points for initiating, consolidating or maintaining the fear extinction memory. i.p. injection of MK-801 at either 40 min before or 4 h after delayed extinction resulted in an impairment of initiating and consolidating fear extinction memory, which caused a long lasting increased freezing score that was still significant on the 7th day after extinction, compared with extinction group. However, MK-801 administered at 12 h after the delayed extinction, when robust consolidation has been occurred and stabilized, did not affect the established extinction memory. Furthermore, the changed freezing behaviors was not due to an alteration in general anxiety levels, since MK-801 treatment had no effect on the percentage of open-arm time or open-arm entries in an Elevated Plus Maze (EPM) task.
CONCLUSIONS/SIGNIFICANCE: Our data suggested that the activation of NMDARs plays important role in initiation and consolidation but not maintenance of fear extinction memory. Together with the fact that NMDA receptor is very important for memory, our data added experimental evidence to the concept that the extinction of conditioned fear responses is a procedure of initiating and consolidating new memory other than simply "erasing" the fear memory.
在听觉恐惧条件反射中,重复呈现音调而不伴随电击会导致习得的恐惧反应的消退。谷氨酸 N-甲基-D-天冬氨酸受体(NMDAR)被认为参与了条件恐惧反应的消退,但它在启动、巩固或维持恐惧消退记忆中的详细作用尚不清楚。在这里,我们使用 NMDAR 拮抗剂 MK-801 来研究这个问题。
方法/主要发现:首先比较了即刻(在条件反射后 10 分钟开始)和延迟(在条件反射后 24 小时开始)消退的效果,结果发现延迟消退导致对条件恐惧反应产生更好、更持久的抑制(在消退后第 20 天仍有显著效果)。在第二个实验中,MK-801 在延迟消退前 40 分钟、4 小时或 12 小时时腹腔内(i.p.)注射,对应于启动、巩固或维持恐惧消退记忆的关键时间点。在延迟消退前 40 分钟或 4 小时 i.p.注射 MK-801 导致启动和巩固恐惧消退记忆受损,导致长时间的冻结评分增加,在消退后第 7 天仍有显著效果,与消退组相比。然而,在延迟消退后 12 小时给予 MK-801,此时已经发生了强大的巩固并稳定下来,不会影响已建立的消退记忆。此外,改变的冻结行为不是由于一般焦虑水平的改变,因为 MK-801 治疗对高架十字迷宫(EPM)任务中开放臂时间或进入开放臂的百分比没有影响。
结论/意义:我们的数据表明,NMDAR 的激活在恐惧消退记忆的启动和巩固中起着重要作用,但在维持中不起作用。结合 NMDA 受体对记忆非常重要的事实,我们的数据为条件性恐惧反应的消退是一个启动和巩固新记忆的过程,而不仅仅是“抹去”恐惧记忆的概念提供了实验证据。