arXiv subjects

Leandro A. A. Aguiar

Publications and source records attributed to Leandro A. A. Aguiar.

5 recordsLinked to original sources

arXiv2025

Revealing stimulus-dependent dynamics through statistical complexity

Advances in large-scale neural recordings have expanded our ability to describe the activity of distributed brain circuits. However, understanding how neural population dynamics differ across regions and behavioral contexts remains challenging. Here, we surveyed neuronal population dynamics across multiple mouse brain areas (visual cortex, hippocampus, thalamus, and midbrain) using spike data from local ensembles. Two complementary measures were used to characterize these dynamics: the coefficient of variation (CV), a classical indicator of spike-time variability, and statistical complexity, an information-theoretic quantifier of organizational structure. To probe stimulus-dependent activity, we segmented and concatenated recordings from behavioral experiments into distinct time series corresponding to natural image presentations, blank screens during visual task, and spontaneous activity. While the CV failed to discriminate between these conditions, statistical complexity revealed clear, stimulus-specific motifs in population activity. These results indicate that information-theoretic measures can uncover structured, stimulus-dependent patterns in neural population dynamics that remain unobserved in traditional variability metrics.

q-bio.NC↗

arXiv2023

State-dependent complexity of the local field potential in the primary visual cortex

The local field potential (LFP) is as a measure of the combined activity of neurons within a region of brain tissue. While biophysical modeling schemes for LFP in cortical circuits are well established, there is a paramount lack of understanding regarding the LFP properties along the states assumed in cortical circuits over long periods. Here we use a symbolic information approach to determine the statistical complexity based on Jensen disequilibrium measure and Shannon entropy of LFP data recorded from the primary visual cortex (V1) of urethane-anesthetized rats and freely moving mice. Using these information quantifiers, we find consistent relations between LFP recordings and measures of cortical states at the neuronal level. More specifically, we show that LFP's statistical complexity is sensitive to cortical state (characterized by spiking variability), as well as to cortical layer. In addition, we apply these quantifiers to characterize behavioral states of freely moving mice, where we find indirect relations between such states and spiking variability.

q-bio.NC↗

arXiv2020

Statistical complexity is maximized close to criticality in cortical dynamics

Complex systems are typically characterized as an intermediate situation between a complete regular structure and a random system. Brain signals can be studied as a striking example of such systems: cortical states can range from highly synchronous and ordered neuronal activity (with higher spiking variability) to desynchronized and disordered regimes (with lower spiking variability). It has been recently shown, by testing independent signatures of criticality, that a phase transition occurs in a cortical state of intermediate spiking variability. Here, we use a symbolic information approach to show that, despite the monotonical increase of the Shannon entropy between ordered and disordered regimes, we can determine an intermediate state of maximum complexity based on the Jensen disequilibrium measure. More specifically, we show that statistical complexity is maximized close to criticality for cortical spiking data of urethane-anesthetized rats, as well as for a network model of excitable elements that presents a critical point of a non-equilibrium phase transition.

q-bio.NC↗

arXiv2020

Subsampled directed-percolation models explain scaling relations experimentally observed in the brain

Recent experimental results on spike avalanches measured in the urethane-anesthetized rat cortex have revealed scaling relations that indicate a phase transition at a specific level of cortical firing rate variability. The scaling relations point to critical exponents whose values differ from those of a branching process, which has been the canonical model employed to understand brain criticality. This suggested that a different model, with a different phase transition, might be required to explain the data. Here we show that this is not necessarily the case. By employing two different models belonging to the same universality class as the branching process (mean-field directed percolation) and treating the simulation data exactly like experimental data, we reproduce most of the experimental results. We find that subsampling the model and adjusting the time bin used to define avalanches (as done with experimental data) are sufficient ingredients to change the apparent exponents of the critical point. Moreover, experimental data is only reproduced within a very narrow range in parameter space around the phase transition.

q-bio.NC↗

arXiv2020

Signatures of brain criticality unveiled by maximum entropy analysis across cortical states

It has recently been reported that statistical signatures of brain criticality, obtained from distributions of neuronal avalanches, can depend on the cortical state. We revisit these claims with a completely different and independent approach, employing a maximum entropy model to test whether signatures of criticality appear in urethane-anesthetized rats. To account for the spontaneous variation of cortical state, we parse the time series and perform the maximum entropy analysis as a function of the variability of the population spiking activity. To compare data sets with different number of neurons, we define a normalized distance to criticality that takes into account the peak and width of the specific heat curve. We found an universal collapse of the normalized distance to criticality dependence on the cortical state on an animal by animal basis. This indicates a universal dynamics and a critical point at an intermediate value of spiking variability.

q-bio.NC↗