Evelyn F. and William L. McKnight Brain Institute, Gainesville, Florida, USA.
Department of Neuroscience, University of Florida, Gainesville, Florida, USA.
Hippocampus. 2021 Jul;31(7):701-716. doi: 10.1002/hipo.23316. Epub 2021 Feb 19.
Mnemonic similarity task performance, in which a known target stimulus must be distinguished from similar lures, is supported by the hippocampus and perirhinal cortex. Impairments on this task are known to manifest with advancing age. Interestingly, disrupting hippocampal activity leads to mnemonic discrimination impairments when lures are novel, but not when they are familiar. This observation suggests that other brain structures support discrimination abilities as stimuli are learned. The prefrontal cortex (PFC) is critical for retrieval of remote events and executive functions, such as working memory, and is also particularly vulnerable to dysfunction in aging. Importantly, the medial PFC is reciprocally connected to the perirhinal cortex and neuron firing in this region coordinates communication between lateral entorhinal and perirhinal cortices to presumably modulate hippocampal activity. This anatomical organization and function of the medial PFC suggests that it contributes to mnemonic discrimination; however, this notion has not been empirically tested. In the current study, rats were trained on a LEGO object-based mnemonic similarity task adapted for rodents, and surgically implanted with guide cannulae targeting prelimbic and infralimbic regions of the medial PFC. Prior to mnemonic discrimination tests, rats received PFC infusions of the GABA agonist muscimol. Analyses of expression of the neuronal activity-dependent immediate-early gene Arc in medial PFC and adjacent cortical regions confirmed muscimol infusions led to neuronal inactivation in the infralimbic and prelimbic cortices. Moreover, muscimol infusions in PFC impaired mnemonic discrimination performance relative to the vehicle control across all testing blocks when lures shared 50-90% feature overlap with the target. Thus, in contrast hippocampal infusions, PFC inactivation impaired target-lure discrimination regardless of the novelty or familiarity of the lures. These findings indicate the PFC plays a critical role in mnemonic similarity task performance, but the time course of PFC involvement is dissociable from that of the hippocampus.
记忆相似性任务表现,即必须从相似的诱饵中区分已知的目标刺激,这一过程得到了海马体和旁嗅皮层的支持。随着年龄的增长,人们已知这种任务会出现损伤。有趣的是,当诱饵是新的时,破坏海马体活动会导致记忆辨别损伤,但当诱饵是熟悉的时则不会。这一观察结果表明,当刺激被学习时,其他大脑结构支持辨别能力。前额叶皮层(PFC)对远程事件和执行功能(如工作记忆)的检索至关重要,并且在衰老过程中也特别容易出现功能障碍。重要的是,内侧前额叶皮层与旁嗅皮层是相互连接的,该区域的神经元放电协调外侧内嗅皮层和旁嗅皮层之间的通信,可能调节海马体的活动。内侧前额叶皮层的这种解剖结构和功能表明它有助于记忆辨别;然而,这一观点尚未得到实证检验。在当前的研究中,大鼠在一种基于乐高物体的记忆相似性任务中接受训练,该任务是为啮齿动物改编的,并接受了针对内侧前额叶皮层的额前叶和下额前叶区域的引导套管手术植入。在进行记忆辨别测试之前,大鼠接受了内侧前额叶皮层的 GABA 激动剂 muscimol 输注。内侧前额叶皮层和相邻皮质区域中神经元活动依赖性即时早期基因 Arc 的表达分析证实, muscimol 输注导致下额前叶和额前叶皮质的神经元失活。此外,与载体对照相比,当诱饵与目标具有 50-90%的特征重叠时,PFC 中的 muscimol 输注会在所有测试块中损害记忆辨别表现。因此,与海马体输注不同,PFC 失活会损害目标-诱饵辨别,而不管诱饵的新颖性或熟悉性如何。这些发现表明,PFC 在记忆相似性任务表现中起着关键作用,但 PFC 的参与时间与海马体的参与时间是分离的。