# Resource-dependent heterosynaptic spike-timing-dependent plasticity in recurrent networks with and without synaptic degeneration

**Authors:** James Humble

PMC · DOI: 10.3389/fncom.2025.1593837 · Frontiers in Computational Neuroscience · 2025-07-22

## TL;DR

This paper introduces a new STDP learning rule that allows stable learning in recurrent networks and compensates for synaptic degeneration.

## Contribution

A novel resource-dependent STDP rule that enables stable learning and compensates for synaptic degeneration in recurrent networks.

## Key findings

- A resource-based STDP rule balances potentiation and depression for synaptic homeostasis.
- The learning rule supports stable activity in recurrent networks without runaway potentiation.
- The rule inherently compensates for synaptic degeneration.

## Abstract

Many computational models that incorporate spike-timing-dependent plasticity (STDP) have shown the ability to learn from stimuli, supporting theories that STDP is a sufficient basis for learning and memory. However, to prevent runaway activity and potentiation, particularly within recurrent networks, additional global mechanisms are commonly necessary. A STDP-based learning rule, which involves local resource-dependent potentiation and heterosynaptic depression, is shown to enable stable learning in recurrent spiking networks. A balance between potentiation and depression facilitates synaptic homeostasis, and learned synaptic characteristics align with experimental observations. Furthermore, this resource-based STDP learning rule demonstrates an innate compensatory mechanism for synaptic degeneration.

## Full-text entities

- **Genes:** Gria1 (glutamate ionotropic receptor AMPA type subunit 1) [NCBI Gene 50592] {aka GluA1, gluR-A}, Ctnnb1 (catenin beta 1) [NCBI Gene 84353] {aka Catnb}
- **Diseases:** Parkinson's (MESH:D010300), Alzheimer's (MESH:D000544), Depression (MESH:D003866), Huntington's (MESH:D006816), schizophrenia (MESH:D012559), neurodegenerative diseases (MESH:D019636), neuropsychiatric disorders (MESH:D001523), spine (MESH:D016135)
- **Chemicals:** dopamine (MESH:D004298), Ca2+ (-), noradrenaline (MESH:D009638), nicotine (MESH:D009538)
- **Species:** Rattus norvegicus (brown rat, species) [taxon 10116]

## Full text

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## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12321831/full.md

## References

57 references — full list in the complete paper: https://tomesphere.com/paper/PMC12321831/full.md

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Source: https://tomesphere.com/paper/PMC12321831