Life has returned to full normalcy. No more trips in the immediate future, no more moving, no more bizarre scheduling for at least a month. Life is good. And time is a little bit more available.
I have completed my second class, "The Motor Basis of Movement." It was a good class to take. I was able to re-learn some things I'd forgotten about the motor system, and was given some insight into the current thinking of the new research. All very exciting.
Below is my term paper. Now again, because of the possibility that this might be stolen for class use (don't do it, it's copyrighted), I have not only left it fairly unpolished and unelaborated, but I have also left off many references that I could have put in. I left the 2 that I found most interesting.
I don't know if an experiment like this would work. Any experts in the field that happen to read my little proposal can let me know if I'm nuts. If so, I would love some comments.
My next class will be "Mechanisms of Drug Actions." Wish me luck. And no, no drugs will be taken during the course of this course.
Renaisauce
Neurobiology of Movement Summer 2008
Changes in Motor Cortical Neuron Representation After Learning Mirror-Image Motor Tasks
Introduction
The motor cortex has historically consisted of regions of neurons that control parts of the body. Recent research has indicated that such a viewpoint is oversimplified. For example, research by Hatsopolous et al. has shown that individual motor neurons react to complex movement patterns (2007). Furthermore, stimulation experiments in primates using 1 second trains have shown patterns in appendage localization (Gracciano et al. 2002). These experiments indicate that small neuronal populations encodes complex 4 dimensional movements that, when taken together, form the large network that allows animals to participate in their full ranges of motion.
It is assumed that each motor neuron and each circuit in the motor cortex (and, by extension, the entire motor system) acquires its specific properties during the course of bodily development and early life experience. It is unclear if individual neurons can change their properties in adulthood, when the network is presumably well-established, and if an imposed change of property would have direct ramifications in the behavior of the animal, or if there would be a compensatory response by other local neurons in the network.
I propose an attempt to alter the neuronal movement encoding of a population of neurons in the motor cortex through a re-entrainment of the directional preference of individual motor neurons. If this neuronal property were to be alterable, information on the mechanisms of that change would be very useful for understanding the details about fine motor control, and would have practical ramifications in the design of brain-machine interfaces and artificial prosthetics.
Materials and Methods
Implants
I propose using a number of rhesus monkeys (obtained and kept according to ethical guidelines). 4-5 Animals would be trained to perform a motor task that yields a food reward. A grid of 24 microelectrodes would be implanted along the primary motor cortex in a permanent headset fixture, which would be left in place for 2 weeks prior to initiation of the learning trials. A control group of 2 monkeys would also receive the surgery and would be set aside. Preferably, headsets would contain a small transmitter and battery that would allow the headset to be independent of any constraining cables. Transmission would send input to a computer monitoring information 24/7, allowing for review of data at the leisure of the researcher.
Tasks
The goal of the first learned task would be the rotation of a wheel counterclockwise. The wheel would be enough of a diameter (perhaps a 20 centimeters in diameter) to necessitate the monkey using its entire arm in the rotation. Full 360° rotation of the wheel would cause a small sugar pellet to be revealed from a dispenser. Reward would only be delivered at certain times of day (as indicated by a red light in the room) so that the dietary and circadian patterns remain consistent and are not interrupted.
As the monkey learns the rotation task, intracellular recordings from the microelectrodes would be analyzed, in conjunction with simultaneous video recording, to discover which cells are most involved with each phase of the rotation sequence. Ideally, neurons would be grouped into four, representing the four quadrants of a circle. One group that seems highly active in moving towards the top of the circle may be different then those that move it towards the bottom. Some adjustments on that protocol would have to be made depending on the neurons that happen to be touching the microelectrodes. Friction would be added to the axel so that the fastest the wheel could be turned by a monkey is 4 seconds (1 second per quadrant).
Once the task is learned and repeated for the course of the week, and the direction-based firing properties of the neurons are known, the counter-clockwise wheels will be replaced with clockwise wheels that provide the same function. A stopper would be added so that movement in the counter-clockwise direction would not be possible. As the monkeys learn to perform the task of rotation, neuron groups would be tested to see if there is any overlap across the neurons involved in counter-clockwise rotation and clockwise rotation. The hypothesis is that, as the two functions are mirror images, there would be minimal overlap.
If overlap proves to be minimal, the next task will be attempt to entrain the neurons involved in clockwise rotation to fire in counterclockwise rotation. As the monkey rotates the wheel in real time, small stimulations (5 V, or the maximum delivery capacity of the microelectrodes) in 100Hz trains, would be delivered to those neurons that fire predominantly during movement in the opposite direction. For example, neurons that would fire normally during a movement up and to the right would be stimulated during the movement up and to the left. This would be done for all four quadrants of the circle. The actual stimulation of the electrodes would be synchronized directly to the rotation of the wheel itself, through preprogramming with the known electrode properties, to eliminate human error in timing. Stimulations would last during the time that monkey spends in a particular wheel quadrant, which should be no less then 1 second.
The stimulation protocol would be carried out over the course of 1 month, providing ample time for any permanent plastic changes to take place. Regular recordings through the microelectrodes would then resume. The firing patterns of the neurons which previously reacted to counterclockwise turns would be analyzed and compared to those that normally fired during clockwise turns to see if there is any change or alignment. Once results were obtained, a counterclockwise wheel would then be reinstalled in order to examine if any changes in firing pattern held true, and to examine the time course, if any, of the neuronal firing preference to return to baseline conditions.
References
Graziano MSA, Taylor CSR, Moore T and Cooke DF. “The Cortical Control of Movement Revisited.” Neuron 36: 349-362.
Hatsopolous NG, Xu G and Amit Y. (2007) “Encoding of Movement Fragments in the Motor Cortex.” J. Neurosci. 27:5105-5144.