This study investigates mean-square spectral instability in network-organized FitzHugh-Nagumo systems under multiplicative noise. By linearizing the stochastic dynamics and analyzing the spectrum of the second-moment operator, we state the exact mean-square stability condition and derive an explicit, generally conservative, spectral condition obtained with the Lyapunov choice $ P = I $. The framework distinguishes direct noise acting on the membrane-potential variable, recovery-channel noise, and their combined influence. Numerical simulations illustrate how these noise channels and network connectivity change finite-network variability and synchronization diagnostics. Direct noise more strongly shifts the determinant component of the conservative spectral boundary in the parameter regimes studied, whereas recovery-channel noise produces a more gradual change. The results provide a mathematical and numerical framework for studying noise-dependent second-moment stability in excitable networks; they are not intended as evidence for clinical seizure regulation or as a demonstrated neuromodulation strategy.
Citation: Bing Zhou, Manrui Zhou, Xiangrong Liu, Qianqian Zheng. Mean-square spectral stability of stochastic FitzHugh–Nagumo networks with noise[J]. AIMS Mathematics, 2026, 11(9): 30619-30642. doi: 10.3934/math.20261213
This study investigates mean-square spectral instability in network-organized FitzHugh-Nagumo systems under multiplicative noise. By linearizing the stochastic dynamics and analyzing the spectrum of the second-moment operator, we state the exact mean-square stability condition and derive an explicit, generally conservative, spectral condition obtained with the Lyapunov choice $ P = I $. The framework distinguishes direct noise acting on the membrane-potential variable, recovery-channel noise, and their combined influence. Numerical simulations illustrate how these noise channels and network connectivity change finite-network variability and synchronization diagnostics. Direct noise more strongly shifts the determinant component of the conservative spectral boundary in the parameter regimes studied, whereas recovery-channel noise produces a more gradual change. The results provide a mathematical and numerical framework for studying noise-dependent second-moment stability in excitable networks; they are not intended as evidence for clinical seizure regulation or as a demonstrated neuromodulation strategy.
| [1] | J. D. Murray, Mathematical biology Ⅱ: spatial models and biomedical applications, 3 Eds., New York: Springer, 2003. https://doi.org/10.1007/b98869 |
| [2] |
M. X. Chen, X. Z. Li, C. R. Tian, Determining Turing instability of the periodic solution of a predator–prey model, Appl. Math. Lett., 171 (2025), 109689. https://doi.org/10.1016/j.aml.2025.109689 doi: 10.1016/j.aml.2025.109689
|
| [3] |
M. X. Chen, Pattern dynamics of a Lotka-Volterra model with taxis mechanism, Appl. Math. Comput., 484 (2025), 129017. https://doi.org/10.1016/j.amc.2024.129017 doi: 10.1016/j.amc.2024.129017
|
| [4] |
A. M. Turing, The chemical basis of morphogenesis, Phil. Trans. R. Soc. B, 237 (1952), 37–72. https://doi.org/10.1098/rstb.1952.0012 doi: 10.1098/rstb.1952.0012
|
| [5] |
H. Nakao, A. S. Mikhailov, Turing patterns in network-organized activator-inhibitor systems, Nature Phys., 6 (2010), 544–550. https://doi.org/10.1038/nphys1651 doi: 10.1038/nphys1651
|
| [6] |
M. Asllani, J. D. Challenger, F. S. Pavone, L. Sacconi, D. Fanelli, The theory of pattern formation on directed networks, Nat. Commun., 5 (2014), 4517. https://doi.org/10.1038/ncomms5517 doi: 10.1038/ncomms5517
|
| [7] |
S. Mimar, M. Asllani, J. D. Challenger, D. Fanelli, Turing patterns mediated by network topology in homogeneous active systems, Phys. Rev. E, 99 (2019), 062303. https://doi.org/10.1103/PhysRevE.99.062303 doi: 10.1103/PhysRevE.99.062303
|
| [8] |
Q. Q. Zheng, J. W. Shen, Y. Xu, Turing instability in the reaction-diffusion network, Phys. Rev. E, 102 (2020), 062215. https://doi.org/10.1103/PhysRevE.102.062215 doi: 10.1103/PhysRevE.102.062215
|
| [9] |
T. Butler, N. Goldenfeld, Fluctuation-driven Turing patterns, Phys. Rev. E, 84 (2011), 011112. https://doi.org/10.1103/PhysRevE.84.011112 doi: 10.1103/PhysRevE.84.011112
|
| [10] |
T. Biancalani, L. Dyson, A. J. McKane, Noise-induced Turing patterns: Physical mechanisms and scaling laws, Phys. Rev. Lett., 112 (2014), 038101. https://doi.org/10.1103/PhysRevLett.112.038101 doi: 10.1103/PhysRevLett.112.038101
|
| [11] |
X. H. Xu, J. Y. Zhang, W. H. Zhang, Mean square exponential stability of stochastic neural networks with reaction-diffusion terms and delays, Appl. Math. Lett., 24 (2011), 5–11. https://doi.org/10.1016/j.aml.2010.07.002 doi: 10.1016/j.aml.2010.07.002
|
| [12] |
R. Xiao, Q. Y. Gao, S. Azaele, Y. Z. Sun, Effects of noise on the critical points of Turing instability in complex ecosystems, Phys. Rev. E, 108 (2023), 014407. https://doi.org/10.1103/PhysRevE.108.014407 doi: 10.1103/PhysRevE.108.014407
|
| [13] |
Z. Q. Wang, Y. Xu, Y. G. Li, T. Kapitaniak, J. Kurths, Chimera states in coupled Hindmarsh-Rose neurons with $\alpha$-stable noise, Chaos Soliton. Fract., 148 (2021), 110976. https://doi.org/10.1016/j.chaos.2021.110976 doi: 10.1016/j.chaos.2021.110976
|
| [14] |
M. Asllani, T. Biancalani, D. Fanelli, Stochastic Turing patterns on a network, Phys. Rev. E, 86 (2012), 046105. https://doi.org/10.1103/PhysRevE.86.046105 doi: 10.1103/PhysRevE.86.046105
|
| [15] |
F. Yu, X. Q. Wang, Y. Xiao, Y. He, W. Yao, S. Cai, et al., Extreme multistability in discrete memristive neuron maps and implications for dual-field applications, Integration, 109 (2026), 102688. https://doi.org/10.1016/j.vlsi.2026.102688 doi: 10.1016/j.vlsi.2026.102688
|
| [16] |
F. Yu, X. Q. Wang, R. Y. Guo, Z. J. Ying, Y. He, Q. Zou, Discrete neuron models and memristive neural network mapping: A comprehensive review, Chinese Phys. B, 34 (2025), 120501. https://doi.org/10.1088/1674-1056/ae0a3b doi: 10.1088/1674-1056/ae0a3b
|
| [17] |
F. Yu, R. Y. Guo, M. F. Zheng, W. Yao, D. D. Zhang, S. Cai, Novel approach to time series forecasting based on memristive Hopfield Neural Network with hidden heterogeneous and homogeneous extreme multistability, Chaos Soliton. Fract., 210 (2026), 118626. https://doi.org/10.1016/j.chaos.2026.118626 doi: 10.1016/j.chaos.2026.118626
|
| [18] |
A. A. Faisal, L. P. J. Selen, D. M. Wolpert, Noise in the nervous system, Nat. Rev. Neurosci., 9 (2008), 292–303. https://doi.org/10.1038/nrn2258 doi: 10.1038/nrn2258
|
| [19] |
M. D. McDonnell, L. M. Ward, The benefits of noise in neural systems: Bridging theory and experiment, Nat. Rev. Neurosci., 12 (2011), 415–425. https://doi.org/10.1038/nrn3061 doi: 10.1038/nrn3061
|
| [20] |
M. Masoliver, N. Malik, E. Schöll, A. Zakharova, Coherence resonance in networks of FitzHugh-Nagumo systems, Chaos, 27 (2017), 101102. https://doi.org/10.1063/1.5003237 doi: 10.1063/1.5003237
|
| [21] |
L. Colombani, P. Toulouse, Propagation of chaos in FitzHugh-Nagumo mean field networks, Mathematical Neuroscience and Applications, 3 (2023), 1–50. https://doi.org/10.46298/mna.9748 doi: 10.46298/mna.9748
|
| [22] |
M. Gerster, R. Berner, J. Sawicki, A. Zakharova, A. Škoch, J. Hlinka, et al., FitzHugh-Nagumo oscillators on complex networks mimic epileptic-seizure-related synchronization phenomena, Chaos, 30 (2020), 123130. https://doi.org/10.1063/5.0021420 doi: 10.1063/5.0021420
|
| [23] |
T. Chouzouris, I. Omelchenko, A. Zakharova, J. Hlinka, P. Jiruska, E. Schöll, Chimera states in brain networks: Empirical neural vs. modular fractal connectivity, Chaos, 28 (2018), 045112. https://doi.org/10.1063/1.5009812 doi: 10.1063/1.5009812
|
| [24] |
J. Cubillos-Cornejo, M. E. Mendoza, I. Bordeu, Extreme events at the onset of epileptic-like intermittent activity of FitzHugh–Nagumo oscillators on small-world networks, Chaos Soliton. Fract., 192 (2025), 116000. https://doi.org/10.1016/j.chaos.2025.116000 doi: 10.1016/j.chaos.2025.116000
|
| [25] |
Z. H. Wang, Z. H. Liu, A Brief Review of Chimera State in Empirical Brain Networks, Front. Physiol., 11 (2020), 724. https://doi.org/10.3389/fphys.2020.00724 doi: 10.3389/fphys.2020.00724
|
| [26] |
R. G. Andrzejak, C. Rummel, F. Mormann, K. Schindler, All together now: Analogies between chimera state collapses and epileptic seizures, Sci. Rep., 6 (2016), 23000. https://doi.org/10.1038/srep23000 doi: 10.1038/srep23000
|
| [27] |
F. Han, D. G. Fang, L. Y. Zhang, Q. Y. Wang, Neurological disease and cognitive dynamics (Ⅰ): Dynamics and control of epileptic seizures, Advances in Mechanics, 52 (2022), 339–396. https://doi.org/10.6052/1000-0992-21-064 doi: 10.6052/1000-0992-21-064
|
| [28] |
L. Y. Zhang, Q. Y. Wang, G. Baier, Spontaneous transitions to focal-onset epileptic seizures: A dynamical study, Chaos, 30 (2020), 103114. https://doi.org/10.1063/5.0021693 doi: 10.1063/5.0021693
|
| [29] |
S. G. Hou, X. T. Liu, Y. Yu, Q. Y. Wang, Functional modal feature analysis based on the network transition dynamics of epileptic seizure, Chaos Soliton. Fract., 197 (2025), 116500. https://doi.org/10.1016/j.chaos.2025.116500 doi: 10.1016/j.chaos.2025.116500
|
| [30] |
J. Y. Zhao, Q. Y. Wang, Y. Yu, A new pathway for controlling absence seizures by reducing GABA uptake from astrocytes: a dynamical perspective, Commun. Nonlinear Sci., 149 (2025), 108929. https://doi.org/10.1016/j.cnsns.2025.108929 doi: 10.1016/j.cnsns.2025.108929
|
| [31] |
M. Kantner, E. Schöll, S. Yanchuk, Delay-induced patterns in a two-dimensional lattice of coupled oscillators, Sci. Rep., 5 (2015), 8522. https://doi.org/10.1038/srep08522 doi: 10.1038/srep08522
|