Oxytocin (OT) is a neuropeptide that modulates social behaviors and the social brain. The effects of OT on the social brain can be tracked by assessing the neural activity in the resting and task states, providing a system-level framework for characterizing state-based functional relationships of its distinct effect. Here, we contribute to this framework by examining how OT modulates social brain network correlations during the resting and task states using fMRI. Firstly, we investigated

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... activation, followed by analyzing the relationship between networks and individual differences measured by the Positive and Negative Affect Schedule and the Big-Five scales. Subsequently, we evaluated functional connectivity in both states. Finally, the relationship between networks across the states was represented by the predictive power of networks in the resting state for task-evoked activity. The difference in predicted accuracy between subjects displayed individual variations in this relationship. Our results showed decreased dorsal default mode network (DDMN) for OT group in the resting state. Additionally, only in the OT group, the activity of the DDMN in the resting state had the largest predictive power for task-evoked activation of the precuneus network (PN). The results also demonstrated OT reduced individual variation of PN, specifically, the difference of accuracy between predicting a subject's own and others' PN task activation. These findings suggest a distributed but modulatory effect of OT on the association between resting brain networks and task-dependent brain networks, showing increased DDMN to PN connectivity after OT administration, which may support OT-induced distributed processing during task performance.