Flexibility of intrinsic neural timescales during distinct behavioral states

Abstract

Recent neuroimaging studies demonstrate a heterogeneity of timescales prevalent in the brain’s ongoing spontaneous activity, labeled intrinsic neural timescales (INT). At the same time, neural timescales also reflect stimulus- or task-related activity. The relationship of the INT during the brain’s spontaneous activity with their involvement in task states including behavior remains unclear. To address this question, we combined calcium imaging data of spontaneously behaving mice and human electroencephalography (EEG) during rest and task states with computational modeling. We obtained four primary findings: (i) the distinct behavioral states can be accurately predicted from INT, (ii) INT become longer during behavioral states compared to rest, (iii) INT change from rest to task is correlated negatively with the variability of INT during rest, (iv) neural mass modeling shows a key role of recurrent connections in mediating the rest-task change of INT. Extending current findings, our results show the dynamic nature of the brain’s INT in reflecting continuous behavior through their flexible rest-task modulation possibly mediated by recurrent connections. Calcium imaging of spontaneously behaving mice show increased intrinsic neural timescales during behavior. The behavioral state of mice can be predicted from the topography of timescales of the cortex. Findings are replicated on a human EEG dataset. Mathematical modeling shows the role of recurrent connections for the change in timescales.