AI Article Synopsis

  • The text discusses how traditional assumptions about Hebbian synaptic plasticity and its role in forming stable memory-encoding neuron groups (cell assemblies) are challenged by new findings.
  • It reveals that when only relying on Hebbian plasticity, cell assemblies tend to fade or diverge, failing to match observed distributions of synaptic strengths.
  • The authors propose that introducing intrinsic spine dynamics can help stabilize these assemblies, though they also suggest that overly strong spine dynamics may negatively impact learning, particularly in conditions like autism spectrum disorder.

Article Abstract

It is often assumed that Hebbian synaptic plasticity forms a cell assembly, a mutually interacting group of neurons that encodes memory. However, in recurrently connected networks with pure Hebbian plasticity, cell assemblies typically diverge or fade under ongoing changes of synaptic strength. Previously assumed mechanisms that stabilize cell assemblies do not robustly reproduce the experimentally reported unimodal and long-tailed distribution of synaptic strengths. Here, we show that augmenting Hebbian plasticity with experimentally observed intrinsic spine dynamics can stabilize cell assemblies and reproduce the distribution of synaptic strengths. Moreover, we posit that strong intrinsic spine dynamics impair learning performance. Our theory explains how excessively strong spine dynamics, experimentally observed in several animal models of autism spectrum disorder, impair learning associations in the brain.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6585147PMC
http://dx.doi.org/10.3389/fncom.2019.00038DOI Listing

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