Showing posts with label motor. Show all posts
Showing posts with label motor. Show all posts

Friday, October 16, 2020

Brain–Machine Interfaces: Closed-Loop Control in an Adaptive System

Edit: I'm pleased to announce that the in-press preprint is now available from Annual Reviews [pdf].

During the first pandemic lockdown in 2020, I had the pleasure of preparing an introductory review on brain-machine interfaces with Ethan Sorrell. It will be published in the 2021 Annual Review of Control, Robotics, and Autonomous Systems. The review is in press now, but I thought I'd share a little sneak peak by way of some figures.

More figures and clip-art are on github. The clip art and figure components are free to reuse (CC NY-NC 4), but Annual Reviews owns the copyright to composed figures and sub-figures.

Friday, March 20, 2015

Motor cortex LFP spatiotemporal dynamics in a cued grasp with instructed delay task

Update: Portions of these notes have now been published in the Journal of Neurophysiology as  "Dissociation between sustained single-neuron spiking and transient β-LFP oscillations in primate motor cortex" and "Phase reorganization leads to transient β-LFP spatial wave patterns in motor cortex during steady-state movement preparation".

[get notes as PDF]

Task-locked modulations in neural activity

The Cued Grasp with Instructed Delay (CGID) task reliably elicits task-locked activity in all three motor areas (M1, PMd, PMv).

  • Consistent with prior literature, the movement period of the CGID task is marked by slow motor evoked potentials (Fig. 2), increased single-unit firing rates (Fig. 3), and beta suppression (Fig. 4).
  • Beta oscillations are enhanced during the first four seconds of the task, although there are some differences between subjects.
  • The average level of beta-LFP synchrony is correlated with beta-LFP power, and varies across phases of the task.
  • We find no evidence of task-locked phase resetting of beta LFP oscillations
  • The spatiotemporal structure of beta-LFP waves is correlated with amplitude and synchrony, with lower amplitudes reflecting more complex wave structures, and higher amplitudes as more synchronous.

figure1

Figure 1: The CGID task reliably elicits evoked potentials, which correlate with beta suppression. In subject S, beta power is strongest in the first second before object presentation. In subject R, beta oscillations are more variable, with somewhat stronger power between the grip and go cues. In both animals, high beta power appears to correspond to periods of higher beta synchrony, and larger phase gradient directionality, a measure of how much LFP activity resembles a plane wave. Conversely, increases in the average magnitude of the Hilbert phase gradient, which summarizes how quickly beta phase changes over the array, and in the number of critical points in the Hilbert phase gradient, which summarizes the complexity of the beta spatiotemporal wave patterns, correspond to periods of beta suppression.