Department of Biological Sciences, University of Alberta, Edmonton, AL, T6G 2E9, Canada.
Department of Neuroscience, UF Scripps Institute for Biomedical Innovation & Technology, 130 Scripps Way, Jupiter, FL, 33458, USA.
Mol Psychiatry. 2024 Sep;29(9):2810-2820. doi: 10.1038/s41380-024-02521-9. Epub 2024 Mar 26.
Recent and pioneering animal research has revealed the brain utilizes a variety of molecular, cellular, and network-level mechanisms used to forget memories in a process referred to as "active forgetting". Active forgetting increases behavioral flexibility and removes irrelevant information. Individuals with impaired active forgetting mechanisms can experience intrusive memories, distressing thoughts, and unwanted impulses that occur in neuropsychiatric diseases. The current evidence indicates that active forgetting mechanisms degrade, or mask, molecular and cellular memory traces created in synaptic connections of "engram cells" that are specific for a given memory. Combined molecular genetic/behavioral studies using Drosophila have uncovered a complex system of cellular active-forgetting pathways within engram cells that is regulated by dopamine neurons and involves dopamine-nitric oxide co-transmission and reception, endoplasmic reticulum Ca signaling, and cytoskeletal remodeling machinery regulated by small GTPases. Some of these molecular cellular mechanisms have already been found to be conserved in mammals. Interestingly, some pathways independently regulate forgetting of distinct memory types and temporal phases, suggesting a multi-layering organization of forgetting systems. In mammals, active forgetting also involves modulation of memory trace synaptic strength by altering AMPA receptor trafficking. Furthermore, active-forgetting employs network level mechanisms wherein non-engram neurons, newly born-engram neurons, and glial cells regulate engram synapses in a state and experience dependent manner. Remarkably, there is evidence for potential coordination between the network and cellular level forgetting mechanisms. Finally, subjects with several neuropsychiatric diseases have been tested and shown to be impaired in active forgetting. Insights obtained from research on active forgetting in animal models will continue to enrich our understanding of the brain dysfunctions that occur in neuropsychiatric diseases.
近期和开创性的动物研究揭示了大脑利用多种分子、细胞和网络水平的机制来遗忘记忆,这个过程被称为“主动遗忘”。主动遗忘增加了行为的灵活性,去除了不相关的信息。主动遗忘机制受损的个体可能会经历侵入性记忆、痛苦的想法和不受控制的冲动,这些都是神经精神疾病的表现。目前的证据表明,主动遗忘机制会降解或掩盖突触连接中“记忆细胞”的分子和细胞记忆痕迹,这些痕迹是特定记忆的特异性。使用果蝇进行的综合分子遗传/行为研究揭示了记忆细胞中主动遗忘途径的复杂系统,该系统受多巴胺神经元调节,涉及多巴胺-一氧化氮共传递和接收、内质网 Ca 信号和受小 GTP 酶调节的细胞骨架重塑机制。其中一些分子细胞机制已经在哺乳动物中被发现是保守的。有趣的是,一些途径独立地调节不同记忆类型和时间阶段的遗忘,这表明遗忘系统具有多层次的组织。在哺乳动物中,主动遗忘还涉及通过改变 AMPA 受体运输来调节记忆痕迹突触强度。此外,主动遗忘采用网络水平的机制,其中非记忆细胞、新生成的记忆细胞和神经胶质细胞以状态和经验依赖性的方式调节记忆细胞突触。值得注意的是,有证据表明网络和细胞水平的遗忘机制之间存在潜在的协调。最后,一些患有多种神经精神疾病的患者也被测试过,结果显示他们的主动遗忘能力受损。从动物模型中对主动遗忘的研究中获得的见解将继续丰富我们对神经精神疾病中大脑功能障碍的理解。