Over 1.7 million people suffer from limb loss in the United States and this number is estimated to increase by 185,000 per year for upper extremity loss. Robotic limbs are highly sophisticated, achieving similar movements compared to the human counterparts, can contain sensors that measure direction and speed of motion, and can be covered with advanced synthetic electronic skin that can detect changes in temperature, humidity, and pressure. Amputees can control their prosthetic limbs by implanted electrodes in their premotor cortex or in the peripheral nerves that can detect volitional intent and translate it into movement of the robotic limb. However, evoking a naturalistic sensation from the engineered sensors in the bionic limb remains a formidable challenge. A fundamental limitation lies in the fact that such signals are conveyed to the user through electrical stimulation of the peripheral nerves, which contain a mixed modality of motor and sensory populations, many of which are indiscriminately depolarized during electrical stimulation, thus producing abnormal tingling, buzzing or burning sensation. Specific sensory modality percepts such as proprioception, mechanoception, nociception or thermoception cannot be reproducibly elicited. Thus, despite much progress in electronic skin sensors and robotic prosthetic devices, this information cannot be naturistically conveyed to the users. This limitation is critical as it obligates users to rely on visual feedback to move and position their prosthetic limbs; such cognitive burden discourages the use of advanced robotic prosthesis. Therefore, there is a need to develop closed-looped interfaces that incorporate somatosensory information vital for achieving stable and adaptive motor control, particularly for grasp and manipulation tasks where visual feedback alone is insufficient. The goal of this study is to develop modality-defined neural interfaces capable of specifically recording from motor neurons and stimulating modality-specific sensory neurons with high selectivity and stability.
We aim to 1) define the selectivity and potency of neuron- and glial-derived growth factors for in vivo chemotaxis of motor and sensory neurons; 2) to evaluate the degree by which axon type submodalities can be segregated from a regenerating mixed population nerve using competitive attractants; and 3) to decode movement intent, and evoke modality-specific sensation via molecularly guided neural interfacing.

Public Health Relevance

Over 1.7 million people suffer from limb loss in the United States and this number is estimated to increase by 185,000 per year for upper extremity loss. While the sophistication level of limb prosthetics has increased dramatically, the usability and provision of natural sensory feedback has remained limited, due in part to the lack of selective and sensitive neural interfacing. We propose to develop high selectivity regenerative neural interfacing in which specific modality percepts can be evoked by selective molecular guidance of motor and sensory subtype axonal regeneration.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
High Priority, Short Term Project Award (R56)
Project #
1R56NS095046-01A1
Application #
9293878
Study Section
Bioengineering of Neuroscience, Vision and Low Vision Technologies Study Section (BNVT)
Program Officer
Gnadt, James W
Project Start
2016-07-15
Project End
2017-06-30
Budget Start
2016-07-15
Budget End
2017-06-30
Support Year
1
Fiscal Year
2016
Total Cost
$403,884
Indirect Cost
$126,051
Name
University of Texas-Dallas
Department
Biomedical Engineering
Type
Schools of Engineering
DUNS #
800188161
City
Richardson
State
TX
Country
United States
Zip Code
75080
Anand, Sanjay; Desai, Vidhi; Alsmadi, Nesreen et al. (2017) Asymmetric Sensory-Motor Regeneration of Transected Peripheral Nerves Using Molecular Guidance Cues. Sci Rep 7:14323