# Building a realistic, scalable memory model with independent engrams using a homeostatic mechanism

## TL;DR

This paper introduces a memory model that forms multiple independent engrams using structural plasticity and homeostatic mechanisms, enabling realistic and scalable simulations.

## Contribution

The novel contribution is a scalable model allowing simultaneous formation of multiple non-interfering memory engrams with high neurophysiological accuracy.

## Key findings

- The model uses structural plasticity and Euclidean distance-based synapse formation to simulate 4 million neurons with 343 memory engrams.
- Synaptic pruning precedes and enables engram formation, differing from Hebbian plasticity mechanisms.
- The model supports long-reaching associations by adjusting simulation parameters.

## Abstract

Memory formation is usually associated with Hebbian learning and synaptic plasticity, which changes the synaptic strengths but omits structural changes. A recent study suggests that structural plasticity can also lead to silent memory engrams, reproducing a conditioned learning paradigm with neuron ensembles. However, this study is limited by its way of synapse formation, enabling the formation of only one memory engram. Overcoming this, our model allows the formation of many engrams simultaneously while retaining high neurophysiological accuracy, e.g., as found in cortical columns. We achieve this by substituting the random synapse formation with the Model of Structural Plasticity. As a homeostatic model, neurons regulate their activity by growing and pruning synaptic elements based on their current activity. Utilizing synapse formation based on the Euclidean distance between the neurons with a scalable algorithm allows us to easily simulate 4 million neurons with 343 memory engrams. These engrams do not interfere with one another by default, yet we can change the simulation parameters to form long-reaching associations. Our model's analysis shows that homeostatic engram formation requires a certain spatiotemporal order of events. It predicts that synaptic pruning precedes and enables synaptic engram formation and that it does not occur as a mere compensatory response to enduring synapse potentiation as in Hebbian plasticity with synaptic scaling. Our model paves the way for simulations addressing further inquiries, ranging from memory chains and hierarchies to complex memory systems comprising areas with different learning mechanisms.