Computing the effects of excitatory-inhibitory balance on neuronal input-output properties

In sensory systems, stimuli are represented through the diverse firing responses and receptive fields of neurons. These features emerge from the interaction between excitatory (E) and inhibitory (I) neuron populations within the network. Changes in sensory inputs alter this balance, leading to shifts in firing patterns and the input-output properties of individual neurons and the network. Although these phenomena have been extensively investigated experimentally and theoretically, the principles governing how E and I inputs are integrated remain unclear. Here, probabilistic rules are derived to describe how neurons in feedforward inhibitory circuits combine these inputs to generate stimulus-evoked responses. This simple model is broadly applicable, capturing a wide range of response features that would otherwise require multiple separate models, and offers insights into the cellular and network mechanisms influencing the input-output properties of neurons, gain modulation, and the emergence of diverse temporal firing patterns.

Authors

Institutions

Publication Details

Journal
PLoS Computational Biology
Published
2026-03-09
DOI
https://doi.org/10.1371/journal.pcbi.1013958
Primary Topic
Neural dynamics and brain function
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Computing the effects of excitatory-inhibitory balance on neuronal input-output properties

Alex D. Reyes
PLoS Computational Biology
Neural dynamics and brain function
article

Computing the effects of excitatory-inhibitory balance on neuronal input-output properties

Alex D. Reyes
article en

Abstract

In sensory systems, stimuli are represented through the diverse firing responses and receptive fields of neurons. These features emerge from the interaction between excitatory (E) and inhibitory (I) neuron populations within the network. Changes in sensory inputs alter this balance, leading to shifts in firing patterns and the input-output properties of individual neurons and the network. Although these phenomena have been extensively investigated experimentally and theoretically, the principles governing how E and I inputs are integrated remain unclear. Here, probabilistic rules are derived to describe how neurons in feedforward inhibitory circuits combine these inputs to generate stimulus-evoked responses. This simple model is broadly applicable, capturing a wide range of response features that would otherwise require multiple separate models, and offers insights into the cellular and network mechanisms influencing the input-output properties of neurons, gain modulation, and the emergence of diverse temporal firing patterns.

PLoS Computational BiologyVol. 22(3)
New York University (US)
Openalex Percentile: Top 33%
Neural dynamics and brain function
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.