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Article Abstract

Functional brain networks exhibit both cooperative and competitive interactions, yet existing models-assuming purely excitatory long-range coupling-fail to account for the widespread anti-correlations observed in fMRI. Starting from a laminar neural mass framework, where each mass comprises distinct slow (alpha-band) and fast (gamma-band) oscillatory pyramidal subpopulations ( and ), we show how laminar-specific long-range excitatory projections across neural mass parcels can give rise to both cooperation and competition via cross-frequency envelope coupling. We demonstrate that homologous connections across parcels (e.g., or ) induce positive correlations between the infra-slow amplitude fluctuations of alpha band envelopes in each parcel, as well as in the simulated fMRI BOLD signals. Conversely, heterologous connections induce negative correlations. We tested this mechanism by building personalized whole-brain models for a cohort of 60 subjects in two steps. First, we inferred signed inter-parcel generative effective connectivity directly from resting-state fMRI using regularized maximum-entropy (Ising) models. Then we connected laminar neural masses to simulate BOLD dynamics by implementing positive and negative Ising connections via homologous and heterologous projections, respectively. Ising-derived cooperative/competitive connectivity modeling faithfully reproduced both static and dynamic functional connectivity patterns, as well as gamma power-BOLD correlation and partial alpha power-BOLD anticorrelation-outperforming structurally constrained and cooperative-only variants. This further demonstrates that functional data alone suffices to infer individualized connectivity. Together, these results provide a biologically grounded mechanistic model on how long-range excitatory circuits and local cross-frequency interactions shape the balance of cooperation and competition in large-scale brain dynamics.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC12338577PMC
http://dx.doi.org/10.1101/2025.07.09.663817DOI Listing

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