arXiv:2605.04088v1 Announce Type: new
Abstract: Intrinsic channel noise is fundamental to neural processing, yet its state-dependent nature, when constrained by strict Feller boundary conditions, is often overlooked. Here, we demonstrate that this bounded multiplicative noise is not merely a source of jitter but an active dynamical force that fundamentally reshapes neural excitability. Investigating a 5D Hodgkin-Huxley-type cortical pacemaker model, we utilize a full-truncation semi-implicit Euler scheme to ensure rigorous probability conservation and domain-preserving integration. Through comprehensive parameter sweeps, we uncover a rich triphasic landscape of noise-induced transitions dictated by the underlying bifurcation structure. Deep in the subthreshold regime, multiplicative noise acts as a constructive force, triggering stochastic awakening via Kramers escape. Near the subcritical Hopf bifurcation, this evolves into highly robust coherence resonance (CR). Crucially, in the supra-threshold oscillatory regime, our framework reveals a striking dynamical shift: a generalized, noise-accelerated Kramers escape. Under extreme multiplicative noise – characteristic of sparse channel populations – strictly bounded fluctuations actively amplify escape rates from the hyperpolarized slow manifold, transforming regular pacing into high-frequency, irregular bursting. Conductance perturbation experiments confirm the profound biological robustness of this transition. These findings establish a physically rigorous mechanism for how boundary-constrained noise drives high-dimensional oscillators toward states of pathological hyperexcitability.
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