Emergence and maintenance of modularity in neural networks with Hebbian and anti-Hebbian inhibitory STDP

TL;DR

This paper demonstrates that simple spike-timing-dependent plasticity rules, involving both Hebbian and anti-Hebbian inhibitory synapses, can naturally lead to the emergence and stability of modular neural network structures capable of memory encoding without external control mechanisms.

Contribution

It introduces a biologically plausible neural model showing how inhibitory STDP rules can produce stable modular organization and memory consolidation in neural networks.

Findings

Inhibitory STDP rules enable stable module formation.

The network exhibits spontaneous memory recall after learning.

Post-learning activity supports long-term memory consolidation.

Abstract

The modular and hierarchical organization of the brain is believed to support the coexistence of segregated (specialization) and integrated (binding) information processes. A relevant question is yet to understand how such architecture naturally emerges and is sustained over time, given the plastic nature of the brain's wiring. Following evidences that the sensory cortices organize into assemblies under selective stimuli, it has been shown that stable neuronal assemblies can emerge due to targeted stimulation, embedding various forms of synaptic plasticity in presence of homeostatic and/or control mechanisms. Here, we show that simple spike-timing-dependent plasticity (STDP) rules, based only on pre- and post-synaptic spike times, can also lead to the stable encoding of memories in the absence of any control mechanism. We develop a model of spiking neurons, trained by stimuli targeting different subpopulations. The model satisfies some biologically plausible features: (i) it contains excitatory and inhibitory neurons with Hebbian and anti-Hebbian STDP; (ii) neither the neuronal activity nor the synaptic weights are frozen after the learning phase. Instead, the neurons are allowed to fire spontaneously while synaptic plasticity remains active. We find that only the combination of two inhibitory STDP subpopulations allows for the formation of stable modules in the network, with each subpopulation playing a distinctive role. The Hebbian subpopulation controls for the firing activity, while the anti-Hebbian neurons promote pattern selectivity. After the learning phase, the network settles into an asynchronous irregular resting-state. This post-learning activity is associated with spontaneous memory recalls which turn out to be fundamental for the long-term consolidation of the learned memories.