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A biophysical corticostriatal model predicts learning-dependent 7T fMRI dynamics and individual reward bias in humans

Carter, S.; Kuang, Z.; Chesebro, A. G.; Jumana, S. A.; Burke, S.; Pathak, A.; Ratai, E.-M.; Miller, E. K.; Granger, R. H.; Mujica-Parodi, L. R.

2026-05-29 neuroscience
10.64898/2026.05.28.728582 bioRxiv
Show abstract

Circuit-level computational models can do more than explain existing data; they can generate novel hypotheses and capture individual differences in human populations. We demonstrate this using a biophysical corticostriatal model, transforming simulated neuronal activity from local field potential (LFP) into functional magnetic resonance imaging (fMRI) signals via the balloon model, and finally generating behavioral outcomes. We then validate the results against those obtained from human subjects. The model generates a counterintuitive yet testable prediction: learning should decrease cross-regional correlations due to increased striatal asynchrony during consolidation, a prediction confirmed in fMRI data optimized for single-subject-level detection sensitivity. The model further enables single-subject fitting of a behavioral outcome, classifying individuals into those differentially responding to positive versus negative reward bias. Established biomarkers, including activation measured by the amplitude of low-frequency fluctuations and dopaminergic effects on hemodynamic latency, are also conserved across LFP and fMRI scales. These findings reposition circuit models as generative tools for human neuroscience, capable of producing mechanistically grounded hypotheses and parsing individual variation in ways inaccessible to data-driven approaches alone.

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