14Several neuroimaging studies reported that a common set of regions are recruited during 15 action observation and execution and it has been proposed that the modulation of the µ rhythm, 16 in terms of oscillations in the alpha and beta bands might represent the electrophysiological 17 correlate of the underlying brain mechanisms. However, the specific functional role of these bands 18 within the µ rhythm is still unclear. Here, we used magnetoencephalography (MEG) to analyze the 19 spectral and temporal properties of the alpha and beta bands in healthy subjects during an action 20 observation and execution task. 21We associated the modulation of the alpha and beta power to a broad action observation 22 network comprising several parieto--frontal areas previously detected in fMRI studies. Of note, we 23 observed a dissociation between alpha and beta bands with a slow--down of beta oscillations 24
ACCEPTED FOR PUBLICATION -NEUROIMAGE2 compared to alpha during action observation. We hypothesize that this segregation is linked to a 25 different sequence of information processing and we interpret these modulations in terms of 26 internal models (forward and inverse). In fact, these processes showed opposite temporal 27 sequences of occurrence: anterior--posterior during action (both in alpha and beta bands) and 28 roughly posterior--anterior during observation (in the alpha band). The observed differentiation 29 between alpha and beta suggests that these two bands might pursue different functions in the 30 action observation and execution processes.
32Keywords: action observation and execution, alpha and beta rhythms, Event--Related 33Desynchronization (ERD), magnetoencephalography (MEG), internal models 34 35 36
INTRODUCTION 37Several studies report that our sensorimotor system is activated when we observe an 38 action performed by other people. This putative mirror--like activity in humans was found in the 39 precentral gyrus (vPM), the inferior frontal gyrus (IFG), the inferior parietal lobule (IPL), and 40 regions within the intraparietal sulcus (for a review see Rizzolatti and Sinigaglia, 2010). In addition 41 to this limited number of regions, neuroimaging studies observed a broader action observation 42 network (AON) which seems to be involved during action observation (OBS) and execution (EXE) 43 (Avenanti et al., 2012;Buccino et al., 2004;Gazzola and Keysers, 2009). A proposed theoretical 44 framework postulates that such AON implements forward and inverse internal models (Wolpert 45 and Ghahramani, 2000), which should be engaged during EXE and OBS. The internal models can 46 account both for how we link our actions to sensory consequences and how others' actions match 47 our own actions and sensations (Gazzola and Keysers, 2009;Iacoboni, 2005). It has been proposed 48 that the fronto--parietal AON has a predictive nature and according to this hypothesis, during 49 action observation the inverse and forward models are integrated to achieve a prediction of 50
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