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Pedro V. Carelli

Publications and source records attributed to Pedro V. Carelli.

13 recordsLinked to original sources

Multifractal human signals at the edge of life reveal a heart-brain anti-correlation

This study investigates the terminal breakdown of human neurophysiological function through the lens of non-linear dynamics by analyzing the multifractal spectrum. Using Multifractal Detrended Fluctuation Analysis (MF-DFA), we quantify the temporal evolution of complexity in synchronized electroencephalogram (EEG) and electrocardiogram (ECG) time series from patients in the terminal stage. Our results reveal a marked divergence in multifractal spectrum width: while neural activity exhibits a collapse of multifractality toward a more constrained state, cardiac signals undergo anomalous spectral broadening, indicating increased non-linear fluctuations and dynamical instability. A negative correlation between these spectral widths suggests effective functional decoupling and the emergence of anti-correlated dynamics between neural and cardiac systems. Rather than reflecting a uniform physiological decline, this divergence is consistent with a body-to-brain breakdown in which peripheral dysfunction progressively overwhelms central regulatory processes. In a broader context, the observed opposing trends resemble patterns reported in other body-driven adaptive processes, suggesting that inverse dynamics across coupled systems may emerge when constraints originate from peripheral rather than central mechanisms. Ultimately, the dying process appears to represent an extreme form of cross-system disintegration, marked by the collapse of the hierarchical coordination that normally sustains integrated physiological function.

q-bio.NC

Hierarchical organization of critical brain dynamics

The hierarchical organization of the brain is a fundamental structural principle, while brain criticality is a leading hypothesis for its collective dynamics. However, the connection between structure and signatures of criticality remains an open question. Here, we address this issue by applying phenomenological renormalization group approaches to large-scale neuronal spiking activity from the mouse visual cortex and hippocampus. We find that signatures of criticality are not uniform, but instead vary systematically along the known anatomical hierarchy in both brain systems. Strikingly, the direction along this gradient is inconsistent across different criticality exponents, revealing a nontrivial, measure-dependent organization: exponents based on static properties point to a gradient in one direction, while the exponent based on dynamic properties points in the opposite direction. Moreover, the signatures across the visual system are strongly modulated by the engagement in a visual task. We show that the correlations among criticality markers of different brain regions during active engagement are sufficient to reconstruct the anatomical hierarchy from the dynamics. Scaling exponents closely follow a theoretically predicted scaling relation among them, and covary with the hierarchical position. Our findings provide a direct link between the collective dynamics of neurons and the macroscopic architecture of the brain.

q-bio.NC

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

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

Feedforward and feedback influences through distinct frequency bands between two spiking-neuron networks

Several studies with brain signals suggested that bottom-up and top-down influences are exerted through distinct frequency bands among visual cortical areas. It has been recently shown that theta and gamma rhythms subserve feedforward, whereas the feedback influence is dominated by the alpha-beta rhythm in primates. A few theoretical models for reproducing these effects have been proposed so far. Here we show that a simple but biophysically plausible two-network motif composed of spiking-neuron models and chemical synapses can exhibit feedforward and feedback influences through distinct frequency bands. Differently from previous studies, this kind of model allows us to study directed influences not only at the population level, by using a proxy for the local field potential, but also at the cellular level, by using the neuronal spiking series.

q-bio.NC

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

Anticipated synchronization in human EEG data: unidirectional causality with negative phase-lag

Understanding the functional connectivity of the brain has become a major goal of neuroscience. In many situatons, the relative phase difference, together with coherence patterns, have been employed to infer the direction of the information flow. However, it has been recently shown in local field potential data from monkeys the existence of a synchronized regime in which unidirectionally coupled areas can present both positive and negative phase differences. During the counterintuitive regime, called anticipated synchronization (AS), the phase difference does not reflect the causality. Here we investigate coherence and causality at the alpha frequency band (10 Hz) between pairs of electroencephalogram (EEG) electrodes in humans during a GO/NO-GO task. We show that human EEG signals can exhibit anticipated synchronization, which is characterized by a unidirectional influence from an electrode A to an electrode B, but the electrode B leads the electrode A in time. To the best of our knowledge, this is the first verification of AS in EEG signals and in the human brain. The usual delayed synchronization (DS) regime is also present between many pairs. DS is characterized by a unidirectional influence from an electrode A to an electrode B and a positive phase difference between A and B which indicates that the electrode A leads the electrode B in time. Moreover, we show that EEG signals exhibit diversity in phase relations: the pairs of electrodes can present in-phase, anti-phase, or out-of-phase synchronization with a similar distribution of positive and negative phase differences.

q-bio.NC

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

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

Deterministic chaos in an ytterbium-doped mode-locked fiber laser

We experimentally study the nonlinear dynamics of a femtosecond ytterbium doped mode-locked fiber laser. With the laser operating in the pulsed regime a route to chaos is presented, starting from stable mode-locking, period two, period four, chaos and period three regimes. Return maps and bifurcation diagrams were extracted from time series for each regime. The analysis of the time series with the laser operating in the quasi mode-locked regime presents deterministic chaos described by an unidimensional Rossler map. A positive Lyapunov exponent $λ= 0.14$ confirms the deterministic chaos of the system. We suggest an explanation about the observed map by relating gain saturation and intra-cavity loss.

physics.optics

Anticipated synchronization in neuronal circuits unveiled by a phase-resetting curve analysis

Anticipated synchronization (AS) is a counter intuitive behavior that has been observed in several systems. When AS establishes in a sender-receiver configuration, the latter can predict the future dynamics of the former for certain parameter values. In particular, in neuroscience AS was proposed to explain the apparent discrepancy between information flow and time lag in the cortical activity recorded in monkeys. Despite its success, a clear understanding on the mechanisms yielding AS in neuronal circuits is still missing. Here we use the well-known phase-resetting-curve (PRC) approach to study the prototypical sender-receiver-interneuron neuronal motif. Our aim is to better understand how the transitions between delayed to anticipated synchronization and anticipated synchronization to phase-drift regimes occur. We construct a map based on the PRC method to predict the phase-locking regimes and their stability. We find that a PRC function of two variables, accounting simultaneously for the inputs from sender and interneuron into the receiver, is essential to reproduce the numerical results obtained using a Hodgkin-Huxley model for the neurons. On the contrary, the typical approximation that considers a sum of two independent single-variable PRCs fails for intermediate to high values of the inhibitory connectivity between interneuron. In particular, it looses the delayed-synchronization to anticipated-synchronization transition.

q-bio.NC

Inhibitory loop robustly induces anticipated synchronization in neuronal microcircuits

We investigate the synchronization properties between two excitatory coupled neurons in the presence of an inhibitory loop mediated by an interneuron. Dynamical inhibition together with noise independently applied to each neuron provide phase diversity in the dynamics of the neuronal motif. We show that the interplay between the coupling strengths and external noise controls the phase relations between the neurons in a counter-intuitive way. For a master-slave configuration (unidirectional coupling) we find that the slave can anticipate the master, on average, if the slave is subject to the inhibitory feedback. In this non-usual regime, called anticipated synchronization (AS), the phase of the post-synaptic neuron is advanced with respect to that of the pre-synaptic neuron. We also show that the AS regime survives even in the presence of unbalanced bidirectional excitatory coupling. Moreover, for the symmetric mutually coupled situation, the neuron that is subject to the inhibitory loop leads in phase.

q-bio.NC

Anticipated Synchronization in a Biologically Plausible Model of Neuronal Motifs

Two identical autonomous dynamical systems coupled in a master-slave configuration can exhibit anticipated synchronization (AS) if the slave also receives a delayed negative self-feedback. Recently, AS was shown to occur in systems of simplified neuron models, requiring the coupling of the neuronal membrane potential with its delayed value. However, this coupling has no obvious biological correlate. Here we propose a canonical neuronal microcircuit with standard chemical synapses, where the delayed inhibition is provided by an interneuron. In this biologically plausible scenario, a smooth transition from delayed synchronization (DS) to AS typically occurs when the inhibitory synaptic conductance is increased. The phenomenon is shown to be robust when model parameters are varied within physiological range. Since the DS-AS transition amounts to an inversion in the timing of the pre- and post-synaptic spikes, our results could have a bearing on spike-timing-dependent-plasticity models.

q-bio.NC