In and Out of Criticality? State-Dependent Scaling in the Rat Visual Cortex

Abstract

The presumed proximity to a critical point is believed to endow the brain with scale-invariant statistics, which are thought to confer various functional advantages in terms of its information processing, storage, and transmission capabilities. To assess the relationship between scaling and cortical states, we apply a phenomenological renormalization group analysis to 3-h spiking data recordings from the urethane-anesthetized rat's visual cortex. Under this type of anesthesia, cortical states dynamically shift across a spectrum of synchronization levels, defined by population spiking rate variability. By developing a scaling criterion based on the kurtosis of the momentum-space activity distribution, our study combines the coarse-graining method with state-dependent analysis. We find that scaling signatures only appear as spiking variability surpasses a specified threshold. Notably, within this regime, scaling exponents show relative stability. Conversely, subthreshold activity is primarily asynchronous and fails to meet the scaling criterion. Our results suggest that a wide range of cortical states corresponds to small deviations around a critical point, with the system fluctuating in and out of criticality, spending roughly three-quarters of the experiment duration within a scaling regime. Published by the American Physical Society 2024