153,318 research outputs found

    Amplitude and latency of beta power during a discrete and continuous motor imageries

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    Motor imagery modifies the neural activity within the primary sensorimotor areas of the cortex in a similar way as a real movement. More precisely, beta oscillations (18-25 Hz), which are often considered as a sensorimotor rhythm, show that the amplitude of brain oscillations is modulated before, during, and after a motor imagery. A large number of Brain-Computer Interfaces (BCIs) are based on the detection of motor imagery related features in the electroencephalographic signal. In most BCI experimental paradigms, subjects realize continuous motor imagery, i.e. a prolonged intention of movement, during a time window of a few seconds. Then, the system detects the movement based on the event-related desynchronization (ERD) and the event-related synchronization (ERS) principles. This study shows that a discrete motor imagery, corresponding to a single short motor imagery, would allow a better detection of ERD and ERS patterns than a continuous motor imagery. Indeed, the results of experiments involving 11 healthy subjects suggest that a continuous motor imagery generates a later ERS as well as a more variable and less detectable ERD than discrete motor imagery. This finding suggests an improved experimental paradigm

    Brain Control of Movement Execution Onset Using Local Field Potentials in Posterior Parietal Cortex

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    The precise control of movement execution onset is essential for safe and autonomous cortical motor prosthetics. A recent study from the parietal reach region (PRR) suggested that the local field potentials (LFPs) in this area might be useful for decoding execution time information because of the striking difference in the LFP spectrum between the plan and execution states (Scherberger et al., 2005). More specifically, the LFP power in the 0–10 Hz band sharply rises while the power in the 20–40 Hz band falls as the state transitions from plan to execution. However, a change of visual stimulus immediately preceded reach onset, raising the possibility that the observed spectral change reflected the visual event instead of the reach onset. Here, we tested this possibility and found that the LFP spectrum change was still time locked to the movement onset in the absence of a visual event in self-paced reaches. Furthermore, we successfully trained the macaque subjects to use the LFP spectrum change as a "go" signal in a closed-loop brain-control task in which the animals only modulated the LFP and did not execute a reach. The execution onset was signaled by the change in the LFP spectrum while the target position of the cursor was controlled by the spike firing rates recorded from the same site. The results corroborate that the LFP spectrum change in PRR is a robust indicator for the movement onset and can be used for control of execution onset in a cortical prosthesis
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