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Functional MRI (fMRI) studies have demonstrated that the rodent brain shows a default mode network (DMN) activity similar to that in humans, offering a potential preclinical model both for physiological and pathophysiological studies. However, the neuronal mechanism underlying rodent DMN remains poorly understood. Here, we used electrophysiological data to analyze the power spectrum and estimate the directed phase transfer entropy (dPTE) within rat DMN across three vigilance states: wakeful rest (WR), slow-wave sleep (SWS), and rapid-eye-movement sleep (REMS). We observed decreased gamma powers during SWS compared with WR in most of the DMN regions. Increased gamma powers were found in prelimbic cortex, cingulate cortex, and hippocampus during REMS compared with WR, whereas retrosplenial cortex showed a reverse trend. These changed gamma powers are in line with the local metabolic variation of homologous brain regions in humans. In the analysis of directional interactions, we observed well-organized anterior-to-posterior patterns of information flow in the delta band, while opposite patterns of posterior-to-anterior flow were found in the theta band. These frequency-specific opposite patterns were only observed in WR and REMS. Additionally, most of the information senders in the delta band were also the receivers in the theta band, and vice versa. Our results provide electrophysiological evidence that rat DMN is similar to its human counterpart, and there is a frequency-dependent reentry loop of anterior-posterior information flow within rat DMN, which may offer a mechanism for functional integration, supporting conscious awareness.

Periodic visual stimulation can evoke the steady-state visual potential (SSVEP) in the brain. Owing to its superior characteristics, the SSVEP has been widely used in neural engineering and cognitive neuroscience studies. However, the underlying mechanisms of the SSVEP are not well understood. In this study, we introduced a brain reconfiguration methodology to explore the possible mechanisms of the SSVEP. The EEG data from five periodic stimuli consistently indicated that the periodic visual stimulation could induce resting-state brain network reconfiguration and that the responses evoked by the stimuli were correlated to the network reconfiguration indexes. For each stimulus frequency, larger response amplitudes corresponded to higher reconfiguration indexes from the resting-state network to a stimulus-evoked network. These findings demonstrate that an external periodic visual stimulation can induce the modification of intrinsic oscillatory activities by reconfiguring resting-state activity at a network level, which could facilitate the responses evoked by the stimulus. These findings provide new insights into the response mechanisms of periodic visual stimulation.

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