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Encoding of Depth in Parietal Reach Region (PRR)
Rajan Bhattacharyya, Richard Andersen

Abstract. Technological developments in the past decade have accelerated the pace of research in brain computer interfaces. Multiple research groups across the country are pursuing this area of research as a possible solution to spinal cord injury. The Andersen lab at Caltech specializes in studying brain areas in the parietal cortex, which is associated with vision and motor planning, and in particular the Parietal Reach Region (PRR) which encodes the plan for the next intended reach movement, which is markedly different than the approach taken by other research groups which are using the motor cortex as the source of control signal. The Cortical Prosthetic Project at the Andersen lab has multiple research areas, including the development of an implantable chip to read signals from the parietal cortex, development of computational models for the neural signals involved, development of an online decoding algorithm for the intended movements, and finally the implementation of the real time control of a robotic arm through a brain computer interface.

This project seeks to investigate the encoding of depth by PRR neurons by carrying out experiments that in essence characterize the system. The first experiment will involve training non-human primates to maintain fixed eye positions while reaching to targets at various locations in three dimensional space. The second experiment will have the primates vary eye positions, however maintain fixed reach locations. Subsequently, we will investigate the neural mechanism by which PRR neurons encode the intended three dimensional reach location and develop a computational model to simulate the process. Lastly, we will augment the online decoding algorithm that is under development to decode PRR signals from implanted arrays in non human primates to control a robotic arm in real time to make reaches to locations in three dimensional space.


Parietal cortex is generally associated with processing visual information to plan motor actions. In particular, the posterior parietal cortex is well known for its role in visuo-motor coordinate transformations. This region of the brain contains specialized areas that perform these coordinate transformations in order to plan motor actions in a common reference frame. Studies conducted in this lab show that the Parietal Reach Region (PRR) is involved in planning reaches, and integrates head and eye position signals (using gain fields) to encode the next intended reach in eye centered (or retinal) coordinates, which is advantageous for a number of reasons including the facilitation of hand eye coordination.

Currently, a model for 2D reach target location has been developed, and an online Bayesian decoding algorithm for the next intended reach has been implemented. The model uses the firing rates of PRR neurons with different receptive fields to predict the location of the intended reach by using Bayes rule to find the most likely target location (currently, only discrete locations are used) from the observed firing rates (see Figure 1). The next step in this project seeks to assess how a) reach depth with constant fixation depth, and b) fixation depth with constant reach depth modulate the PRR signal. In a sense, through the two types of modulation above, we hope to characterize the system and develop a computational model of how 3D target locations for the next intended reach are coded by Parietal Reach Region neurons.

It is unknown how depth vision and reaching in depth modulates PRR neurons. When a subject proceeds to fixate an object of interest in the visual scene, the brain uses various cues to position the eyes correctly and modify of the lens for focus. For objects within a close of distance (6ft, and certainly within reach distance), eye position can fully specify where the subject is fixating, and in particular, the amount the eyes rotate inward, called the vergence angle, specify where in depth the subject of fixating (accommodation, or the focusing of the lenses in the eyes is very rarely out of register with vergence angle). Other objects at different depths from the fixation depth in the visual scene have binocular disparity (a difference in position of the image of the object cast on the two retinas); binocular disparity provides the information that the brain uses to calculate the depth or distance to these objects relative to the fixation depth. By presenting fixation stimuli at different depths, measuring eye position (vergence angle), and presenting reach targets in depth (with known binocular disparities), we seek to understand how the PRR signals are modulated by these parameters (See Figure 2).

Eye position is measured with the scleral search coil technique, and neural recordings will be obtained by the implantation of micromachined silicon or tungsten electrode arrays. Our experimental setup consists of a track of LEDs, which will serve as fixation targets, and a 3 axis Cartesian robot arm with an attached touch sensor as the reach target. The implantation of the arrays will be performed stereotaxically, with the aid of an MRI to localize the region of implantation before surgery. A 32 channel Plexon data acquisition system is in place for recording from the arrays, and all stimuli (LEDs and robot arm) are administered by a real time operating system through LabView (National Instruments).

The outlined experiments will provide the data necessary to develop a computational model of the PRR neurons. The phasic activity of the PRR neurons are understood and broken into various epochs, wherein the firing rate during the memory/planning period determines the location of the next intended reach. The form of the model will be to express firing rate of a PRR neuron as a function of fixation distance and reach depth, and will most likely be nonlinear. The general expected result is that reach depth will be represented as a gain field (Andersen et al. 1985), wherein the tuning curve of the neuron, or in this case, two dimensional receptive field in the frontoparallel plane, is simply multiplied by a constant proportional to the reach depth. This is the result found in a close by brain area also located in the intraparietal sulcus, LIP, which signals the next intended eye movement (Gnadt and Mays, 1995). Currently, it is unknown how fixation depth will be represented in the activity of the PRR neurons, however it is likely that it results in gain modulation as well; we expect that the firing rate function will be nonlinear, and that the gain modulation will be nonlinear as well. Additionally, we will attempt white noise analysis, or the reverse correlation technique to plot a three dimensional receptive field for a PRR neuron, however this can only be done by holding one parameter constant (such as fixation distance, so [reach] depth becomes relative to this).

Once a computational model is verified, the final goal of this research is to augment the online decoding algorithm to decode three dimensional intended reach location. This will then be used to control a prosthetic device to physically move to the location of the intended reach. In order to accomplish this, two robot arms will be in place, one to present the stimulus and the other for the primate to control with its thoughts (PRR online decoding controls the arm). The success of these experiments will then allow the implantation of electrode arrays in patients suffering from spinal cord injury in an attempt to control prosthetic devices.

This project advances neuroscience and the understanding of the Parietal Reach Region as well as integrating math and engineering techniques for the development of the computational model. In addition, the research involved in developing an implantable chip for recording signals furthers the ultimate goal of the robust and dependable brain computer interface. Most importantly, the efforts in truly understanding the neural signal to develop a real time decoding algorithm is the most important aspect in this project because acceptable reliability and accuracy has not been achieved by other methods in this area of research, and is critical to the success of any cortical prosthetic project.

References
Andersen RA and Buneo CA. Intentional Maps in the Posterior Parietal Cortex. Annual Review of Neuroscience, 2002.
Batista AP and Andersen RA. The parietal reach region codes the next planned movement in a sequential reach task. Journal of Neurophysiology 85: 539:544, 2001.
Buneo CA, Jarvis MR, Batista AP and Andernes RA. Direct visuomotor transformations fo reaching. Nature 416:632:636, 2002.
Cumming BG and DeAngelis GC. The physiology of stereopsis. Annual Review of Neuroscience 24: 203-238, 2001.
Gnadt JW and Mays LE. Neurons in mokey parietal area LIP are tuned for eye movement parameters in three dimensional space. Journal of Neurophysiology 73:280-297, 1995
Meeker D, Shenoy KV, Cao S, Pesaren B, Scherberger H, Jarvis M, Buneo CA, Batista AP, Kureshi SA, Mitra PP, Burdick JW, and Andersen RA. Cognitive control signals for prosthetic systems. Society of Neuroscience Abstracts 27, 2001.
Rosenbluth D and Allman JM. The effect of gaze angle and fixation distance on the responses of neurons in V1, V2, and V4. Neuron 33:143:149, 2002.


Figure 1. Bayesian Decoding of PRR activity from several neurons. (Cao, 2001)

Figure 2. Red = Fixation Point, Blue = Reach Target. The image cast by the red point is in the same location on the retina (the eyes are rotated inward [vergence angle] specifically for this, whereas the blue target is on different locations (disparity).


Figure 2. Simulated result. This neuron prefers 20cm reach


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