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Ediline L. F. Nguessap

Publications and source records attributed to Ediline L. F. Nguessap.

3 recordsLinked to original sources

Influence of astrocyte feedback and noise on breathing neural clusters

Astrocytes are increasingly recognized as active regulators of neural dynamics, yet their role in large-scale synchronization remains incompletely understood. Building on the discovery of breathing cluster synchronization in neuron-astrocyte networks, we investigate whether this phenomenon persists under more biologically realistic conditions by incorporating thermosensitive neuronal dynamics, intrinsic electric-field interactions, stochastic perturbations, and delayed astrocytic feedback. Through systematic numerical simulations of a network containing structurally symmetric neuronal subsets, we show that breathing clusters characterized by intermittent alternations between synchronized and desynchronized states, remain robust across a broad range of biophysical conditions. The results reveal a non-monotonic dependence on astrocytic attenuation and feedback parameters, with intermediate values maximizing rhythmic switching through a slow push-pull regulatory mechanism. Temperature and electric-field effects primarily modulate neuronal excitability and the tolerance of the breathing state to noise, while elevated stochastic perturbations progressively destabilize cluster coherence. In contrast, the phenomenon exhibits remarkable robustness to biologically realistic astrocytic delays. Importantly, our findings indicate that the emergence of breathing synchronization remains fundamentally governed by the interplay between network symmetry and astrocyte-mediated feedback, whereas temperature, electric fields, and noise act as modulators of its stability and temporal organization. These results establish breathing cluster synchronization as a robust organizing principle of astrocyte-regulated networks and provide a quantitative framework for understanding how glial regulation shapes cortical state-switching under realistic physiological conditions.

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Modulation of Neuronal Firing Modes by Electric Fields in a Thermosensitive FitzHugh-Nagumo Model

We introduce a thermosensitive FitzHugh-Nagumo neuron model extended with a third dynamic variable representing an external electric field. This unified framework enables a biophysically grounded analysis of how combined thermal and electrical stimuli modulate neuronal excitability. The model incorporates temperature dependence, ion charge density, cell radius, and voltage-driven stimulation, capturing their joint effects on membrane polarization and firing dynamics. Using bifurcation analysis, Lyapunov exponents, and interspike interval variability, we identify transitions between spiking, bursting, and chaotic regimes. We further show how periodic electric fields tune these dynamics as a function of stimulus amplitude, frequency, and cellular geometry. Our results provide mechanistic insights into neuronal excitability and suggest avenues for controlling neural activity via hybrid thermal-electrical modulation, with potential applications in neuromodulation therapies and bioelectronics.

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Dynamic effects of electric field in hybrid coupling thermosensitive neuronal network

The dynamics of thermosensitive FitzHugh--Nagumo neuronal networks under hybrid synaptic coupling and external electric fields are investigated in a ring topology. Numerical simulations show collective behavior ranging from incoherent activity to coherent traveling waves and chimera and multichimera states, arising from the interplay between thermosensitivity, intrinsic electric fields, and the balance between electrical and chemical synapses. Chemical nonlocal coupling is essential for the stabilization of traveling waves and traveling chimera patterns, whereas purely electrical local coupling of chaotic neurons yields only incoherent states. The frequency and spatial extent of the applied field act as key control parameters: low frequencies and localized stimulation can induce or suppress chimera-like domains, while high frequencies have negligible impact on network dynamics. Intrinsic electric fields, controlled by the cell radius r, modulate single-neuron excitability and reshape the network response to external fields, enabling transitions between incoherence, chimera-like states, and global synchronization. These results suggest that weak, spatially targeted electric fields can serve as effective control knobs for complex patterns of activity in thermosensitive hybrid-coupled networks, with potential implications for selective neuromodulation and bio-inspired computing.

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