Paper List
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Macroscopic Dominance from Microscopic Extremes: Symmetry Breaking in Spatial Competition
This paper addresses the fundamental question of how microscopic stochastic advantages in spatial exploration translate into macroscopic resource domi...
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Linear Readout of Neural Manifolds with Continuous Variables
This paper addresses the core challenge of quantifying how the geometric structure of high-dimensional neural population activity (neural manifolds) d...
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Theory of Cell Body Lensing and Phototaxis Sign Reversal in “Eyeless” Mutants of Chlamydomonas
This paper solves the core puzzle of how eyeless mutants of Chlamydomonas exhibit reversed phototaxis by quantitatively modeling the competition betwe...
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Cross-Species Transfer Learning for Electrophysiology-to-Transcriptomics Mapping in Cortical GABAergic Interneurons
This paper addresses the challenge of predicting transcriptomic identity from electrophysiological recordings in human cortical interneurons, where li...
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Uncovering statistical structure in large-scale neural activity with Restricted Boltzmann Machines
This paper addresses the core challenge of modeling large-scale neural population activity (1500-2000 neurons) with interpretable higher-order interac...
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Realizing Common Random Numbers: Event-Keyed Hashing for Causally Valid Stochastic Models
This paper addresses the critical problem that standard stateful PRNG implementations in agent-based models violate causal validity by making random d...
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A Standardized Framework for Evaluating Gene Expression Generative Models
This paper addresses the critical lack of standardized evaluation protocols for single-cell gene expression generative models, where inconsistent metr...
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Single Molecule Localization Microscopy Challenge: A Biologically Inspired Benchmark for Long-Sequence Modeling
This paper addresses the core challenge of evaluating state-space models on biologically realistic, sparse, and stochastic temporal processes, which a...
Pulse desynchronization of neural populations by targeting the centroid of the limit cycle in phase space
University of Padua | Abdus Salam International Center for Theoretical Physics | Université Paris Dauphine-PSL
30秒速读
IN SHORT: This work addresses the core challenge of determining optimal pulse timing and intensity for desynchronizing pathological neural oscillations when the underlying dynamical system is unknown, by leveraging a robust geometric feature in phase space.
核心创新
- Methodology Introduces a pulse desynchronization control strategy based on targeting the geometric centroid of the limit cycle in phase space, a point shown to be robust to changes in the coupling constant (ε).
- Methodology Utilizes bivariate neural activity signals (e.g., X and Y averages) as feedback input, moving beyond traditional univariate approaches (like local field potential alone) to extract richer phase-space information.
- Theory Demonstrates analytically and numerically that the centroid lies within a region of maximal return times to the limit cycle after perturbation, making it an effective target for prolonging desynchronized states with minimal pulses.
主要结论
- Numerical simulations of a coupled FitzHugh-Nagumo system (N=1000) show the centroid's location is nearly independent of the coupling parameter ε (tested for ε ∈ {0.1, 0.2, 0.3, 0.4}), providing a robust target.
- The centroid is strategically located near the dx/dt=0 nullcline within the region of maximal return times (visualized via interpolated heatmaps), delaying the system's return to the synchronized limit cycle.
- The proposed control strategy, exploiting bivariate input and the centroid target, aims to achieve desynchronization with a significantly lower number of pulses compared to previous adaptive search methods, potentially reducing clinical side effects.
摘要: The synchronized activity of neuronal populations can lead to pathological over-synchronization in conditions such as epilepsy and Parkinson disease. Such states can be desynchronized by brief electrical pulses. But when the underlying oscillating system is not known, as in most practical applications, to determine the specific times and intensities of pulses used for desynchronizaton is a difficult inverse problem. Here we propose a desynchronization scheme for neuronal models of bi-variate neural activity, with possible applications in the medical setting. Our main argument is the existence of a peculiar point in the phase space of the system, the centroid, that is both easy to calculate and robust under changes in the coupling constant. This important target point can be used in a control procedure because it lies in the region of minimal return times of the system.