| Literature DB >> 28772119 |
Abstract
Pioneering research studies, beginning with those using Drosophila, have identified several molecular and cellular mechanisms for active forgetting. The currently known mechanisms for active forgetting include neurogenesis-based forgetting, interference-based forgetting, and intrinsic forgetting, the latter term describing the brain's chronic signaling systems that function to slowly degrade molecular and cellular memory traces. The best-characterized pathway for intrinsic forgetting includes "forgetting cells" that release dopamine onto engram cells, mobilizing a signaling pathway that terminates in the activation of Rac1/Cofilin to effect changes in the actin cytoskeleton and neuron/synapse structure. Intrinsic forgetting may be the default state of the brain, constantly promoting memory erasure and competing with processes that promote memory stability like consolidation. A better understanding of active forgetting will provide insights into the brain's memory management system and human brain disorders that alter active forgetting mechanisms.Entities:
Keywords: Rac1; active forgetting; consolidation; dopamine; hippocampal neurogenesis; intrinsic forgetting; memory
Mesh:
Year: 2017 PMID: 28772119 PMCID: PMC5657245 DOI: 10.1016/j.neuron.2017.05.039
Source DB: PubMed Journal: Neuron ISSN: 0896-6273 Impact factor: 17.173