Article ID: 2024EAP1086
Neural interactions under optimal excitatory/inhibitory (E/I) balance are among the most crucial mechanisms for realizing cognitive functions. Among the phenomena supported by this mechanism, the duration of a phenomenon known as perceptual alternation exhibits two representative characteristics: nondeterminism and the long-tailed property at the level of a large neural population. However, even in a system consisting of a single pair of excitatory and inhibitory neurons, called chaos-chaos intermittency (CCI), a similar intermittent alternation of neural activity emerges, involving intermittent transitions between multiple isolated attractors. We hypothesized that the characteristics of CCI dynamics in local excitatory-inhibitory neural circuits can describe the nondeterminism and long-tailed properties observed at a broad hierarchical level. We evaluated the changes in nondeterminism and long-tailed properties under different E/I balance conditions to test this hypothesis. First, we validated the determinism of two types of dynamics: 1) transitions between attractors and 2) behavior within attractors. This evaluation was performed using iterated amplitude-adjusted Fourier transform and multi-scale entropy analysis. Next, we characterize the long-tailed properties of the alternations. These properties were evaluated while gradually shifting the parameters from attractor-merging bifurcation. These results indicate that while behavior within attractors demonstrate determinism across all conditions, transitions between attractors lose nondeterminism as the predominance of excitatory neuron increases. Furthermore, the duration histograms lose their long-tailed properties as excitatory neurons become dominant. Consequently, the disappearance of determinism and long-tailed properties co-occurs, and the coexistence of nondeterminism and long-tailed properties is realized within specific domains of the E/I balance. This discovery contributes to our understanding of the importance of an optimal E/I balance for maintaining the characteristics of interactions between excitatory and inhibitory neurons.
