Functional asymmetries in ON and OFF ganglion cells of primate retina.

Functional asymmetries in the ON and OFF pathways of the primate visual system were examined using simultaneous multi-electrode recordings from dozens of retinal ganglion cells (RGCs) in vitro. Light responses of RGCs were characterized using white noise stimulation. Two distinct functional types of cells frequently encountered, one ON and one OFF, had non-opponent spectral sensitivity, relatively high response gain, transient light responses, and large receptive fields (RFs) that tiled the region of retina recorded, suggesting that they belonged to the same morphological cell class, most likely parasol. Three principal functional asymmetries were observed. (1) Receptive fields of ON cells were 20% larger in diameter than those of OFF cells, resulting in higher full-field sensitivity. (2) ON cells had faster response kinetics than OFF cells, with a 10-20% shorter time to peak, trough and zero crossing in the biphasic temporal impulse response. (3) ON cells had more nearly linear light responses and were capable of signaling decrements, whereas OFF cells had more strongly rectifying responses that provided little information about increments. These findings suggest specific mechanistic asymmetries in retinal ON and OFF circuits and differences in visual performance on the basis of the activity of ON and OFF parasol cells.

Low-dimensional neural features predict muscle EMG signals.

Understanding the relationship between neural activity in motor cortex and muscle activity during movements is important both for basic science and for the design of neural prostheses. While there has been significant work in decoding muscle EMG from neural data, decoders often require many parameters which make the analysis susceptible to overfitting, which reduces generalizability and makes the results difficult to interpret. To address this issue, we recorded simultaneous neural activity from the motor cortices (M1/PMd) of rhesus monkeys performing an arm-reaching task while recording EMG from arm muscles. In this work, we focused on relating the mean neural activity (averaged across reach trials to one target) to the corresponding mean EMG. We reduced the dimensionality of the neural data and found that the curvature of the low-dimensional (low-D) neural activity could be used as a signature of muscle activity. Using this signature, and without directly fitting EMG data to the neural activity, we derived neural axes based on reaches to only one reach target (< 5% of the data) that could explain EMG for reaches across multiple targets (average R(2) = 0.65). Our results suggest that cortical population activity is tightly related to muscle EMG measurements, predicting a lag between cortical activity and movement generation of 47.5 ms. Furthermore, our ability to predict EMG features across different movements suggests that there are fundamental axes or directions in the low-D neural space along which the neural population activity moves to activate particular muscles.

Increasing the performance of cortically-controlled prostheses.

Neural prostheses have received considerable attention due to their potential to dramatically improve the quality of life of severely disabled patients. Cortically-controlled prostheses are able to translate neural activity from cerebral cortex into control signals for guiding computer cursors or prosthetic limbs. Non-invasive and invasive electrode techniques can be used to measure neural activity, with the latter promising considerably higher levels of performance and therefore functionality to patients. We review here some of our recent experimental and computational work aimed at establishing a principled design methodology to increase electrode-based cortical prosthesis performance to near theoretical limits. Studies discussed include translating unprecedentedly brief periods of "plan" activity into high information rate (6.5 bits/s)control signals, improving decode algorithms and optimizing visual target locations for further performance increases, and recording from chronically implanted arrays in freely behaving monkeys to characterize neuron stability. Taken together, these results should substantially increase the clinical viability of cortical prostheses.