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Gontier, C.

Publications and source records attributed to Gontier, C..

3 recordsLinked to original sources

Closed-loop error damping in human BCI using pre-error motor cortex activity

Intracortical brain-computer interfaces (BCIs) are used to decode motor intent from neural population activity; their main clinical application is to restore function for individuals with motor or communication deficits. However, when trying to reconstruct movement trajectories, such as in computer cursor control, even state-of-the-art decoders fall short of able-bodied performance during online BCI control. This calls for alternative approaches to improve the usability of motor BCIs. Here, we leveraged an error signal, i.e. a neural correlate of faulty motor control that can be detected from neural activity. By detecting this error signal in parallel to performing movement decoding, it is possible to perform error modulation, i.e. real-time error detection and correction during a closed-loop motor BCI task. We analyzed data from four individuals with upper limb impairment due to cervical spinal cord injury who each used an intracortical BCI to perform a continuous cursor control task with visual feedback. A classifier was trained to detect the error signal and was used to perform online error detection during BCI control to limit ongoing errors (defined as movement of the controller away from its target) without requiring any specific action from the participants. Our contribution is three-fold. First, we show that the error signal has a pre-error component. Cortical activity was already significantly modulated before the onset of the kinematically-defined error, theoretically allowing for earlier detection. Second, we show that error modulation significantly improves performance during online BCI control of cursor kinematics. Finally, we show that the error signal can be robustly leveraged across contexts, as error modulation improves performance in more complex motor tasks (involving for instance grasp and drag actions) or other environments without task-specific calibration. Overall, our results suggest that the error signal can be robustly disentangled from motor intent in cortical activity, and that even a simple linear classifier can enable error modulation in parallel to a continuous kinematic decoder, yielding more reliable and accurate BCI control.

neuroscience↗

Distinct neural modes carry information about grasp force and phase in the sensorimotor cortex

Humans perform a variety of complex hand movements to manipulate objects, requiring precise control of changing forces. Understanding the role of sensorimotor cortex and the cortical dynamics underlying these actions is crucial for developing interventions that restore dexterous hand function after injury or disease. In this study, two individuals with tetraplegia resulting from cervical spinal cord injury attempted a series of isometric grasps. Neural activity was recorded from the motor and somatosensory cortices using intracortical microelectrode arrays while participants attempted to exert a static force or to ramp force up and down. Despite their inability to execute movement, and with limited afferent input, the spiking activity in motor and somatosensory cortex was modulated with the task. Within the neural response we identified independent neural modes - distinct patterns of population-level neural activity - that were informative about both the timing and magnitude of the force. Moreover, distinct neural modes were observed during static and dynamic grasping conditions, suggesting independent control schemes for maintaining and changing forces. These modes were related to phases of the task, including the onset, offset, holding periods, as well as phases of increasing and decreasing force. These results will inform the design of intracortical brain-computer interface (iBCI) systems that can leverage these naturally occurring patterns of grasp and force control to restore dexterous hand function. Significance StatementRestoring dexterous hand function after injury remains a major challenge, partly due to an incomplete understanding of the cortical dynamics underlying grasping and force control. In this study, we investigated neural activity within the motor and somatosensory cortices of individuals with tetraplegia attempting to perform grasps to different target forces with varying temporal profiles. We identified distinct neural modes modulated during specific phases of grasp that encode force information throughout the task. These findings suggest that brain-computer interfaces could leverage these native neural modes to restore grasping and force modulation.

neuroscience↗

A computational model of altered neuronal activity in altered gravity

Electrophysiological experiments have shown that neuronal activity changes upon exposure to altered gravity. More specifically, neurons firing rates increase during microgravity and decrease during centrifugal-induced hypergravity. Different biophysical explanations have been proposed for this phenomenon: however, they have not been backed by quantitative analyses nor simulations. More generally, classical computational models of neurons and networks do not account for the effect of altered gravity, which limits the possibility to perform in-silico experiments and simulations. Here, we propose computational implementations for different effects of altered gravity on cellular functions, and modify existing models to account for the effect of micro- and hyper-gravity. Firstly, in line with previous experiments, we suggest that microgravity could be modeled as an increase of the voltage-dependent channel transition rates, which is assumed to be the result of a higher membrane fluidity and can be readily implemented into the Hodgkin-Huxley model. Using in-silico simulations of single neurons, we show that this model of the influence of gravity on neuronal activity allows to reproduce the observed increased firing and burst rates. Secondly, we explore the role of mechano-gated (MG) ion channels on population activity. We show that recordings can be fitted by a network of connected excitatory neurons, whose activity is balanced by firing rate adaptation. Adding a small depolarizing current to account for the activation of MG channels also reproduces the observed increased firing and burst rates. Overall, our results fill an important gap in the literature, by providing a computational link between altered gravity and neuronal activity. Starting from historical observations of the effects of gravity on cellular functions, we derived gravity-sensitive models of neurons and networks, whose predictions could be refined using future experiments.

neuroscience↗