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Gorka Zamora-López

Publications and source records attributed to Gorka Zamora-López.

9 recordsLinked to original sources

Functional Whole-Brain Models: A New Framework for Unifying Brain Structure and Cognitive Function

Contemporary computational neuroscience features two prominent modeling traditions. Bottom-up whole-brain modeling (WBM) builds biophysically detailed simulations of brain structure and dynamics, whereas top-down neuroconnectionism optimizes deep neural networks for functional performance. Each has achieved remarkable success yet remains incomplete with WBMs lacking functional competence and neuroconnectionist models showing limited biological grounding. Here we propose functional whole-brain models (fWBMs) as a unified modeling paradigm that integrates structural and dynamical realism with task-performing capacity. fWBMs are defined by four minimal criteria: structural grounding in empirical connectomes and regional biology, continuous-time dynamical realism, functional competence across cognitive domains, and mappable observables to neuroimaging, electrophysiologcal and behavioral data. To formalize this integration, we establish a three-pillar roadmap across short-, mid-, and long-term horizons, and outline the scientific and clinical opportunities this paradigm enables. We argue that the disciplined pursuit of this integrative vision will generate the tools, common language, and cross-scale hypotheses needed to advance our understanding of the brain.

q-bio.NC↗

The global communication pathways of the human brain transcend the cortical-subcortical-cerebellar division

Understanding how cortex, subcortex and cerebellum integrate is a major challenge for neuroscience, however, studies of the brain's structural connectivity have mostly focused on cortico-cortical links. Here, we used diffusion imaging to construct the structural connectome of the entire human brain including 360 cortical, 233 subcortical, and 125 cerebellar regions of interest (ROIs). We found that the brain forms a modular and hierarchical network architecture, organized into modules of mixed cortical, subcortical and/or cerebellar regions, and whose cross-modular pathways are centralized through highly connected hub ROIs (a `rich-club'). This global rich-club is subcortically dominated and, surprisingly, composed of hub ROIs from all subcortical structures rather than one region like the thalamus, centralizing the communication pathways. This study improves our understanding of the human brain's organization. It provides structural evidence to question the prevalent cortico-centric notion by revealing a connectome centered at the subcortex but made of transversal pathways.

q-bio.NC↗

Emergence and maintenance of modularity in neural networks with Hebbian and anti-Hebbian inhibitory STDP

The modular and hierarchical organization of the brain is believed to support the coexistence of segregated (specialization) and integrated (binding) information processes. A relevant question is yet to understand how such architecture naturally emerges and is sustained over time, given the plastic nature of the brain's wiring. Following evidences that the sensory cortices organize into assemblies under selective stimuli, it has been shown that stable neuronal assemblies can emerge due to targeted stimulation, embedding various forms of synaptic plasticity in presence of homeostatic and/or control mechanisms. Here, we show that simple spike-timing-dependent plasticity (STDP) rules, based only on pre- and post-synaptic spike times, can also lead to the stable encoding of memories in the absence of any control mechanism. We develop a model of spiking neurons, trained by stimuli targeting different subpopulations. The model satisfies some biologically plausible features: (i) it contains excitatory and inhibitory neurons with Hebbian and anti-Hebbian STDP; (ii) neither the neuronal activity nor the synaptic weights are frozen after the learning phase. Instead, the neurons are allowed to fire spontaneously while synaptic plasticity remains active. We find that only the combination of two inhibitory STDP subpopulations allows for the formation of stable modules in the network, with each subpopulation playing a distinctive role. The Hebbian subpopulation controls for the firing activity, while the anti-Hebbian neurons promote pattern selectivity. After the learning phase, the network settles into an asynchronous irregular resting-state. This post-learning activity is associated with spontaneous memory recalls which turn out to be fundamental for the long-term consolidation of the learned memories.

q-bio.NC↗

An integrative dynamical perspective for graph theory and the study of complex networks

Built upon the shoulders of graph theory, the field of complex networks has become a central tool for studying real systems across various fields of research. Represented as graphs, different systems can be studied using the same analysis methods, which allows for their comparison. Here, we challenge the wide-spread idea that graph theory is a universal analysis tool, uniformly applicable to any kind of network data. Instead, we show that many classical graph metrics (including degree, clustering coefficient and geodesic distance) arise from a common hidden propagation model: the discrete cascade. From this perspective, graph metrics are no longer regarded as combinatorial measures of the graph, but as spatio-temporal properties of the network dynamics unfolded at different temporal scales. Once graph theory is seen as a model-based (and not a purely data-driven) analysis tool, we can freely or intentionally replace the discrete cascade by other canonical propagation models and define new network metrics. This opens the opportunity to design, explicitly and transparently, dedicated analyses for different types of real networks by choosing a propagation model that matches their individual constraints. In this way, we take stand that network topology cannot always be abstracted independently from network dynamics, but shall be jointly studied. Which is key for the interpretability of the analyses. The model-based perspective here proposed serves to integrate into a common context both the classical graph analysis and the more recent network metrics defined in the literature which were, directly or indirectly, inspired by propagation phenomena on networks.

physics.soc-ph↗

Sizing the length of complex networks

Among all characteristics exhibited by natural and man-made networks the small-world phenomenon is surely the most relevant and popular. But despite its significance, a reliable and comparable quantification of the question `how small is a small-world network and how does it compare to others' has remained a difficult challenge to answer. Here we establish a new synoptic representation that allows for a complete and accurate interpretation of the pathlength (and efficiency) of complex networks. We frame every network individually, based on how its length deviates from the shortest and the longest values it could possibly take. For that, we first had to uncover the upper and the lower limits for the pathlength and efficiency, which indeed depend on the specific number of nodes and links. These limits are given by families of singular configurations that we name as ultra-short and ultra-long networks. The representation here introduced frees network comparison from the need to rely on the choice of reference graph models (e.g., random graphs and ring lattices), a common practice that is prone to yield biased interpretations as we show. Application to empirical examples of three categories (neural, social and transportation) evidences that, while most real networks display a pathlength comparable to that of random graphs, when contrasted against the absolute boundaries, only the cortical connectomes prove to be ultra-short.

physics.soc-ph↗

A novel framework to analyze complex network dynamics

Graph theory constitutes a widely used and established field providing powerful tools for the characterization of complex networks. The intricate topology of networks can also be investigated by means of the collective dynamics observed in the interactions of self-sustained oscillations (synchronization patterns) or propagation-like processes such as random walks. However, networks are often inferred from real data forming dynamic systems, which are different from those employed to reveal their topological characteristics. This stresses the necessity for a theoretical framework dedicated to the mutual relationship between the structure and dynamics in complex networks, as the two sides of the same coin. Here we propose a rigorous framework based on the network response over time (i.e., Green function) to study interactions between nodes across time. For this purpose we define the \emph{flow} that describes the interplay between the network connectivity and external inputs. This multivariate measure relates to the concepts of graph communicability and the map equation. We illustrate our theory using the multivariate Ornstein-Uhlenbeck process, which describes stable and non-conservative dynamics, but the formalism can be adapted to other local dynamics for which the Green function is known. We provide applications to classical network examples, such as small-world ring and hierarchical networks. Our theory defines a comprehensive framework that is canonically related to directed and weighted networks, thus paving a new way to revise the standards for network analysis, from the pairwise interactions between nodes to the global properties of networks including community detection.

physics.soc-ph↗

How structure sculpts function: unveiling the contribution of anatomical connectivity to the brain's spontaneous correlation structure

Intrinsic brain activity is characterized by highly structured co-activations between different regions, whose origin is still under debate. In this paper, we address the question whether it is possible to unveil how the underlying anatomical connectivity shape the brain's spontaneous correlation structure. We start from the assumption that in order for two nodes to exhibit large covariation, they must be exposed to similar input patterns from the entire network. We then acknowledge that information rarely spreads only along an unique route, but rather travels along all possible paths. In real networks the strength of local perturbations tends to decay as they propagate away from the sources, leading to a progressive attenuation of the original information content and, thus, of their influence. We use these notions to derive a novel analytical measure, $\mathcal{T}$ , which quantifies the similarity of the whole-network input patterns arriving at any two nodes only due to the underlying topology, in what is a generalization of the matching index. We show that this measure of topological similarity can indeed be used to predict the contribution of network topology to the expected correlation structure, thus unveiling the mechanism behind the tight but elusive relationship between structure and function in complex networks. Finally, we use this measure to investigate brain connectivity, showing that information about the topology defined by the complex fabric of brain axonal pathways specifies to a large extent the time-average functional connectivity observed at rest.

q-bio.NC↗

Functional complexity emerging from anatomical constraints in the brain: the significance of network modularity and rich-clubs

The large-scale structural ingredients of the brain and neural connectomes have been identified in recent years. These are, similar to the features found in many other real networks: the arrangement of brain regions into modules and the presence of highly connected regions (hubs) forming rich-clubs. Here, we examine how modules and hubs shape the collective dynamics on networks and we find that both ingredients lead to the emergence of complex dynamics. Comparing the connectomes of C. elegans, cats, macaques and humans to surrogate networks in which either modules or hubs are destroyed, we find that functional complexity always decreases in the perturbed networks. A comparison between simulated and empirically obtained resting-state functional connectivity indicates that the human brain, at rest, lies in a dynamical state that reflects the largest complexity its anatomical connectome can host. Last, we generalise the topology of neural connectomes into a new hierarchical network model that successfully combines modular organisation with rich-club forming hubs. This is achieved by centralising the cross-modular connections through a preferential attachment rule. Our network model hosts more complex dynamics than other hierarchical models widely used as benchmarks.

q-bio.NC↗

Chimera-like states in modular neural networks

Chimera states, namely the coexistence of coherent and incoherent behavior, were previously analyzed in complex networks. However, they have not been extensively studied in modular networks. Here, we consider the neural network of the \textit{C.elegans} soil worm, organized into six interconnected communities, where neurons obey chaotic bursting dynamics. Neurons are assumed to be connected with electrical synapses within their communities and with chemical synapses across them. As our numerical simulations reveal, the coaction of these two types of coupling can shape the dynamics in such a way that chimera-like states can happen. They consist of a fraction of synchronized neurons which belong to the larger communities, and a fraction of desynchronized neurons which are part of smaller communities. In addition to the Kuramoto order parameter $ρ$, we also employ other measures of coherence, such as the chimera-like $χ$ and metastability $λ$ indices, which quantify the degree of synchronization among communities and along time, respectively. We perform the same analysis for networks that share common features with the \textit{C.elegans} neural network. Similar results suggest that under certain assumptions, chimera-like states are prominent phenomena in modular networks, and might provide insight for the behavior of more complex modular networks.

nlin.AO↗