Miller Adam M P, Frick Brendan J, Smith David M, Radulovic Jelena, Corcoran Kevin A
Department of Psychology, Cornell University, Ithaca, NY 14853, United States.
Department of Psychiatry and Behavioral Sciences, The Asher Center for the Study and Treatment of Depressive Disorders, Feinberg School of Medicine, Northwestern University, Chicago, IL 60611, United States.
Neurobiol Learn Mem. 2017 Nov;145:59-66. doi: 10.1016/j.nlm.2017.08.010. Epub 2017 Aug 30.
Memory retrieval requires coordinated intra- and inter-regional activity in networks of brain structures. Dysfunction of these networks and memory impairment are seen in many psychiatric disorders, but relatively little is known about how memory retrieval and memory failure are represented at the level of local and regional oscillatory activity. To address this question, we measured local field potentials (LFPs) from mice as they explored a novel context, retrieved memories for contextual fear conditioning, and after administration of two amnestic agents: the NMDA receptor antagonist MK-801 and muscarinic acetylcholine receptor antagonist scopolamine (SCOP). LFPs were simultaneously recorded from retrosplenial cortex (RSC), dorsal hippocampus (DH), and anterior cingulate cortex (ACC), which are involved in processing contextual memories, and analyzed for changes in intra-regional power and inter-regional peak coherence of oscillations across multiple frequency bands. Context encoding and memory retrieval sessions yielded similar patterns of changes across all three structures, including decreased delta power and increased theta peak coherence. Baseline effects of MK-801 and SCOP were primarily targeted to gamma oscillations, but in opposite directions. Both drugs also blocked memory retrieval, as indicated by reduced freezing when mice were returned to the conditioning context, but this common behavioral impairment was only associated with power and peak coherence disruptions after MK-801 treatment. These findings point to neural signatures for memory impairment, whose underlying mechanisms may serve as therapeutic targets for related psychiatric disorders.
记忆提取需要脑结构网络内和区域间的协同活动。这些网络功能障碍和记忆损伤在许多精神疾病中都有出现,但对于记忆提取和记忆失败在局部和区域振荡活动水平上是如何表现的,我们了解得相对较少。为了解决这个问题,我们在小鼠探索新环境、提取情境恐惧条件反射记忆时,以及在给予两种遗忘剂后,测量了它们的局部场电位(LFP):NMDA受体拮抗剂MK-801和毒蕈碱型乙酰胆碱受体拮抗剂东莨菪碱(SCOP)。从参与处理情境记忆的压后皮质(RSC)、背侧海马体(DH)和前扣带回皮质(ACC)同时记录LFP,并分析多个频段振荡的区域内功率和区域间峰值相干性的变化。情境编码和记忆提取阶段在所有三个结构中产生了相似的变化模式,包括δ功率降低和θ峰值相干性增加。MK-801和SCOP的基线效应主要针对γ振荡,但方向相反。两种药物还阻断了记忆提取,当小鼠回到条件化环境时冻结反应减少就表明了这一点,但这种共同的行为损伤仅与MK-801治疗后的功率和峰值相干性破坏有关。这些发现指出了记忆损伤的神经特征,其潜在机制可能成为相关精神疾病的治疗靶点。