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Active Forgetting and Neuropsychiatric Diseases

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Journal Mol Psychiatry
Date 2024 Mar 27
PMID 38532011
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Abstract

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.

References
1.
Owald D, Felsenberg J, Talbot C, Das G, Perisse E, Huetteroth W . Activity of defined mushroom body output neurons underlies learned olfactory behavior in Drosophila. Neuron. 2015; 86(2):417-27. PMC: 4416108. DOI: 10.1016/j.neuron.2015.03.025. View

2.
Stickgold R, Walker M . Sleep-dependent memory triage: evolving generalization through selective processing. Nat Neurosci. 2013; 16(2):139-45. PMC: 5826623. DOI: 10.1038/nn.3303. View

3.
Hodges J, Newell-Litwa K, Asmussen H, Vicente-Manzanares M, Horwitz A . Myosin IIb activity and phosphorylation status determines dendritic spine and post-synaptic density morphology. PLoS One. 2011; 6(8):e24149. PMC: 3162601. DOI: 10.1371/journal.pone.0024149. View

4.
Dudai Y, Karni A, Born J . The Consolidation and Transformation of Memory. Neuron. 2015; 88(1):20-32. DOI: 10.1016/j.neuron.2015.09.004. View

5.
Schwaerzel M, Monastirioti M, Scholz H, Friggi-Grelin F, Birman S, Heisenberg M . Dopamine and octopamine differentiate between aversive and appetitive olfactory memories in Drosophila. J Neurosci. 2003; 23(33):10495-502. PMC: 6740930. View