State-space kinetic Ising model reveals task-dependent entropy flow in sparsely active nonequilibrium neuronal dynamics

TL;DR

This paper introduces a state-space kinetic Ising model to analyze nonstationary, nonequilibrium neuronal dynamics, revealing task-dependent entropy flow and causal interactions in mouse visual cortex during behavior.

Contribution

The study develops a novel state-space kinetic Ising model that captures nonstationary neural activity and estimates entropy flow, advancing understanding of causal dynamics in neural systems.

Findings

Greater variability in causal couplings during task engagement.

Higher entropy flow per spike correlates with better task performance.

Model uncovers asymmetric causal dynamics linked to behavior.

Abstract

Neuronal ensemble activity, including coordinated and oscillatory patterns, exhibits hallmarks of nonequilibrium systems with time-asymmetric trajectories to maintain their organization. However, assessing time asymmetry from neuronal spiking activity remains challenging. The kinetic Ising model provides a framework for studying the causal, nonequilibrium dynamics in spiking recurrent neural networks. Recent theoretical advances in this model have enabled time-asymmetry estimation from large-scale steady-state data. Yet, neuronal activity often exhibits time-varying firing rates and coupling strengths, violating the steady-state assumption. To overcome this limitation, we developed a state-space kinetic Ising model that accounts for nonstationary and nonequilibrium properties of neural systems. This approach incorporates a mean-field method for estimating time-varying entropy flow, a key measure for maintaining the system's organization through dissipation. Applying this method to mouse visual cortex data revealed greater variability in causal couplings during task engagement despite reduced neuronal activity with increased sparsity. Moreover, higher-performing mice exhibited increased coupling-related entropy flow per spike during task engagement, suggesting more efficient computation in the higher-performing mice. These findings underscore the model's utility in uncovering intricate asymmetric causal dynamics in neuronal ensembles and linking them to behavior through the thermodynamic underpinnings of neural computation.