RESUMO
The ability to precisely anticipate the timing of upcoming events at the time-scale of seconds is essential to predict objects' trajectories or to select relevant sensory information. What neurophysiological mechanism underlies the temporal precision in anticipating the occurrence of events? In a recent article,1 we demonstrated that the sensori-motor system predictively controls neural oscillations in time to optimize sensory selection. However, whether and how the same oscillatory processes can be used to keep track of elapsing time and evaluate short durations remains unclear. Here, we aim at testing the hypothesis that the brain tracks durations by converting (external, objective) elapsing time into an (internal, subjective) oscillatory phase-angle. To test this, we measured magnetoencephalographic oscillatory activity while participants performed a delayed-target detection task. In the delayed condition, we observe that trials that are perceived as longer are associated with faster delta-band oscillations. This suggests that the subjective indexing of time is reflected in the range of phase-angles covered by delta oscillations during the pre-stimulus period. This result provides new insights into how we predict and evaluate temporal structure and support models in which the active entrainment of sensori-motor oscillatory dynamics is exploited to track elapsing time.
RESUMO
A cerebral network comprising precuneus, medial frontal, and temporoparietal cortices is less active both during goal-directed behavior and states of reduced consciousness than during conscious rest. We tested the hypothesis that the interictal epileptic discharges affect activity in these brain regions in patients with temporal lobe epilepsy who have complex partial seizures. At the group level, using electroencephalography-correlated functional magnetic resonance imaging in 19 consecutive patients with focal epilepsy, we found common decreases of resting state activity in 9 patients with temporal lobe epilepsy (TLE) but not in 10 patients with extra-TLE. We infer that the functional consequences of TLE interictal epileptic discharges are different from those in extra-TLE and affect ongoing brain function. Activity increases were detected in the ipsilateral hippocampus in patients with TLE, and in subthalamic, bilateral superior temporal and medial frontal brain regions in patients with extra-TLE, possibly indicating effects of different interictal epileptic discharge propagation.