MASSACHUSETTS GENERAL HOSPITAL, THE
The inability to communicate underlies one of the most disabling aspects of injury to the central nervous system, and includes the inability to perform rudimentary tasks such as flexing and extending ones' limb or moving a simple cursor on a screen. While the majority of studies thus far have targeted the intrinsic repair or regeneration of damaged areas of the central nervous system such as brainstem or proximal cervical spinal cord, alternative approaches for redirecting information between areas that remain functionally intact is largely unexplored. Work by our group and others has demonstrated that neuronal activity in cortical and subcortical areas responsible for motor control can accurately predict volitional movement intention, and that delivery of event-related electrical stimuli in areas responsible for motor production can reproducibly alter targeted limb movement. In the current study, we aim to extend these findings by systematically matching and altering motor intent with movement production in primates performing a motor directional task. To this end, we will obtain single-neuronal recording from the same subcortical areas shown to predict motor intention and use a similar system design to deliver electrical stimuli to the ventral spinal cord in order to approximate and alter movement production. Changes in neuronal activity will be examined over multiple trials as observed movements predicted by neuronal activity are made to either correspond or mismatch movements produced by spinal cord stimulation. These findings will provide a unique perspective into the individual roles that motor neuronal plasticity and spinal efferent activity play in adaptive motor control, and may offer valuable new insight into the development of prosthetic designs aimed at restoring volitional movement. PUBLIC HEALTH RELEVANCE: Motor deficit is among the most debilitating aspects of subjects suffering injury to the central nervous system. Despite continued efforts to develop treatments for patients with such injury, there remain few and often no options available for reconstituting volitional motor control. The proposed project aims to explore a novel approach for restoring motor communication that is based on a system design developed by our group for use in awake-behaving primates. The significant social impact of such devices has already been demonstrated with the emergence of cochlear, brainstem and retinal prosthetic implants, and may similarly provide significant benefit for patients with motor disability resulting from brainstem and proximal spinal cord injury.
| AWARD OVERVIEW |
| Award Number |
3R01HD059852-01A1S1 |
Funding Agency |
Department of Health and Human Services |
| Total Award Amount |
$167,958 |
Project Location - City |
Boston |
| Award Date |
09/30/2009 |
Project Location - State |
MA |
| Project Status |
Completed |
Project Location - Zip |
02114-0000
|
| Jobs Reported |
0.71 |
Congressional District |
09 |
| Project Location - Country |
US |
|
|
Recipient Information
(Grants)
| Recipient Information (Grants) |
|
Recipient Name
|
MASSACHUSETTS GENERAL HOSPITAL, THE |
| Recipient DUNS Number |
073130411
|
| Recipient Address |
55 FRUIT ST |
| Recipient City |
BOSTON |
| Recipient State |
Massachusetts |
| Recipient Zip |
02114-2621 |
| Recipient Congressional District |
09 |
| Recipient Country |
USA |
Required to Report Top 5 Highly Compensated Officials |
No |
Projects and Jobs Information
| Projects and Jobs Information |
| Project Title |
Neuronal Based Prothestic Control of Volitional Movement |
| Project Status |
Completed |
| Final Project Report Submitted |
Yes |
| Project Activities Description |
General Medical and Surgical Hospitals |
| Quarterly Activities/Project Description |
The ARRA supplement has two key goals. The first goal has been to hire an additional student in order to dedicate full effort to Aim 2 of the project. The second has been to upgrade our single-channel spinal cord stimulator to a multi-channel stimulator.
With respect to the first goal, we have already hired Keren Haroush, PhD to the lab. Aim 2 of the project is integral to the development of a closed-loop neuronal prosthetic design, and requires a dedicated technical understanding and expertise for neuronal tissue stimulation. Additional experiments have now provided an important addition to the project making the combined aims now more streamlined, efficient and likely to succeed.
With respect to the second goal, we have purchased a new high throughput stimulator, and have begun preliminary testing. We anticipate that it will provide a critical addition to spinal cord stimulation experiments. The upgraded stimulator will allow us to offer a wider range of stimulation sites and amplitude sets that can be controlled through a single program interface. We anticipate that the stimulator will also allow us to produce movement trajectories at high enough resolution to develop and test a functional neuronal prosthetic design able to simulate close to veridical movement. Finally, it will allow us to perform longer-term experiments. We have begin putting the data together on preliminary experiments and writing up some of the results. Some of our initial results with basic stimulation of the spinal cord will be submitted within the next few months. |
| Jobs Created |
0.71 |
| Description of Jobs Created |
The inability to communicate underlies one of the most disabling aspects of injury to the central nervous system, and includes the inability to perform rudimentary tasks such as flexing and extending ones' limb or moving a simple cursor on a screen. While the majority of studies thus far have targeted the intrinsic repair or regeneration of damaged areas of the central nervous system such as brainstem or proximal cervical spinal cord, alternative approaches for redirecting information between areas that remain functionally intact is largely unexplored. Work by our group and others has demonstrated that neuronal activity in cortical and subcortical areas responsible for motor control can accurately predict volitional movement intention, and that delivery of event-related electrical stimuli in areas responsible for motor production can reproducibly alter targeted limb movement. In the current study, we aim to extend these findings by systematically matching and altering motor intent with movement production in primates performing a motor directional task. To this end, we will obtain single-neuronal recording from the same subcortical areas shown to predict motor intention and use a similar system design to deliver electrical stimuli to the ventral spinal cord in order to approximate and alter movement production. Changes in neuronal activity will be examined over multiple trials as observed movements predicted by neuronal activity are made to either correspond or mismatch movements produced by spinal cord stimulation. These findings will provide a unique perspective into the individual roles that motor neuronal plasticity and spinal efferent activity play in adaptive motor control, and may offer valuable new insight into the development of prosthetic designs aimed at restoring volitional movement.
Despite continued efforts to develop treatments for patients with such injury, there remain few and often no options available for reconstituting volitional motor control. The proposed project aims to explore a novel approach for restoring motor communication that is based on a system design developed by our group for use in awake-behaving primates. The significant social impact of such devices has already been demonstrated with the emergence of cochlear, brainstem and retinal prosthetic implants, and may similarly provide significant benefit for patients with motor disability resulting from brainstem and proximal spinal cord injury. In Aim 1 of the parent proposal, single-unit neuronal recordings will be made from the STN of rhesus monkeys as they perform a motor directional task. During each session, regression models will be trained on the response matrix containing the firing rates of the recorded neurons and correlated to the animals? movement. Once the models are trained, neuronal activity recorded on subsequent sessions will be used to predict the primates? intended vector of movement. In Aim 2, microstimulations will be delivered to the ventral spinal cord as the primates perform the same motor directional task. Based on prior stimulation testings, movements previously observed to be induced by spinal cord stimulation will be made to either correspond (approximate) or mismatch the observed movements predicted by neuronal activity. This will therefore allow us to examine the dissociable roles that motor neuronal plasticity and spinal efferent activity play in adaptive motor control. Because this approach does not require a direct ?line of communication? between areas responsible for motor control and those responsible for motor production, it may also offer a unique approach for reconstituting volitional motor communication in patients with central nervous system injury.
|
Purchaser Information
(Grants)
| Purchaser Information |
| Contracting Office ID |
Not Reported |
| Contracting Office Name |
Not Available |
| Contracting Office Region |
Not Available |
| TAS Major Program |
75-0840 |
| Award Information |
| Award Date |
09/30/2009 |
| Award Number |
3R01HD059852-01A1S1 |
| Order Number |
|
| Award Type |
Grants |
| Funding Agency ID |
75 |
| Funding Agency Name |
Department of Health and Human Services |
| Funding Office Name |
Not Available |
| Awarding Agency ID |
75 |
| Awarding Agency Name |
Department of Health and Human Services |
| Amount of Award |
$167,958 |
| Funds Invoiced/Received |
$167,958 |
| Expenditure Amount |
$167,958 |
| Infrastructure Expenditure Amount |
$0 |
| Infrastructure Purpose and Rationale |
Not Reported |
| Infrastructure Point of Contact Name |
Not Reported |
| Infrastructure Point of Contact Email |
Not Reported |
| Infrastructure Point of Contact Phone |
Not Reported |
| Infrastructure Point of Contact Address |
Not Reported |
| Infrastructure Point of Contact City |
Not Reported |
| Infrastructure Point of Contact State |
Not Reported |
| Infrastructure Point of Contact Zip |
Not Reported |
Product or Service Information
(Grants)
| Product or Service Information |
| Primary Activity Code |
622110 |
| Activity Description |
General Medical and Surgical Hospitals |
| Sub-Awards Information |
| Sub-awards to Organizations |
0 |
| Sub-award Amounts to Organizations |
$0 |
| Sub-Awards to Individuals |
0 |
| Sub-Award Amounts to Individuals |
$0 |
| Number of Sub-awards less than $25,000/award |
0 |
| Amount of Sub-awards less than $25,000/award |
$0 |
| Number of payments to vendors greater than $25,000 |
1 |
| Total Amount of payments to vendors greater than $25,000/award |
$80,000 |
| Number of payments to vendors less than $25,000/award |
1 |
| Total Amount of payments to vendors less than $25,000/award |
$427 |
Newport Corporation - Award Number 3R01HD059852-01A1S1 - Newport Corporation
| Award Number |
3R01HD059852-01A1S1 |
| Sub-Award Number |
N/A |
| Vendor DUNS Number |
009145814 |
| Vendor HQ Zip Code + 4 |
92606-4814 |
| Vendor Name |
Newport Corporation |
| Product and Service Description |
Newport N1S Stimulator - will provide up to 32 stimulation-site locations at a time. A high throughput stimulator has multiple benefits that are particularly relevant to this project, and would be highly constructive to its success
|
| Payment Amount |
$80,000 |
| Location Information |
| Latitude, Longitude |
42º 21' 44",
-71º 4' 11" |
| Congressional District |
09 |
| Address 1 |
55 Fruit Street |
| Address 2 |
|
| City |
Boston |
| County |
Suffolk |
| State |
MA |
| Zip |
02114-0000 |
|
 |