Untangling the influence of distinct sources of somatosensory feedback on the neural dynamics of dexterous movement control
Project Number1DP2NS142717-01
Former Number1DP2OD036811-01
Contact PI/Project LeaderKHANNA, PREEYA
Awardee OrganizationUNIVERSITY OF CALIFORNIA BERKELEY
Description
Abstract Text
PROJECT SUMMARY
To move successfully, we must be able to sense our bodies and our environment. This is no more evident
than when participants attempt to strike a match to light a candle after their hand’s somatosensation has been
numbed. Despite being able to see well, participants fumble with the match and clumsily attempt to accomplish
the task. Further, somatosensory-motor integration is notably impaired in many types of neurological movement
disorders including Parkinson’s disease, stroke, essential tremor, and dystonia. Developing rehabilitation or
therapeutic strategies to improve somatosensory-motor integration faces a central challenge: while the
theoretical importance of somatosensory-motor integration (SMI) is clear, how the brain actually processes
afferent signals to enable excellent movement control remains unclear.
In this proposal, we seek to use a population neural dynamics framework to understand how the brain
implements SMI computations. Specifically, we will leverage a novel feedback-dependent dexterous
manipulation task, high-density multi-area recordings, and an innovative type of electrical stimulation that can
be used to modulate inter-area communication in the macaque monkey. These combined experiments and
analysis are designed to uncover how SMI computations, long known to be critical for movement control, are
implemented in population neural activity patterns in brain. Further, they will pave the way for developing
approaches for restoring damaged SMI in the brain after brain injury or neurodegenerative disease.
The main experimental approach of this proposal includes simultaneous high-density, high channel-count
(Neuropixel) electrophysiological recordings from the primary motor cortex (M1), primary somatosensory cortex
(S1), and cerebellar-receiving motor thalamus (mThal) in non-human primates that are learning and executing a
dexterous manipulation task. The main analytical approach includes modeling the timeseries of motor cortical
population activity as a combination of intrinsic motor cortical dynamics and inputs from S1 and mThal. The
hypothesis of this proposal is that S1 and mThal exert different influences on M1 population dynamics throughout
the learning and execution process. Specifically, we hypothesize that S1 provides specific sensory updates that
drive M1 population activity, and mThal modulates the temporal dynamics of M1 population activity. We will
further develop evidence for or against this hypothesis by leveraging a novel neuromodulation approach that can
boost or interrupt communication between distant brain regions. Completion of this proposal will constitute an
understanding of how SMI computations, that have long been thought to be essential for movement, are actually
implemented in the circuitry and population dynamics of the macaque sensorimotor system. This advance would
improve our understanding of how to target somatosensory nodes to improve control of movement following
motor impairment.
Public Health Relevance Statement
PROJECT NARRATIVE
To move successfully, we must be able to sense our bodies and our environment. While
theoretical work outlines computations that ought to take place for successful integration of
somatosensation into movement, how population neural activity in somatosensory and motor
nodes in the brain interact to accomplish this integration remains unclear. This proposal uses
multi-area electrophysiology to monitor functional interactions in distributed sensorimotor nodes
during the acquisition and execution of a dexterous manipulation task, mapping theoretical
computations onto the circuits and cross-area population dynamics in the sensorimotor network.
National Institute of Neurological Disorders and Stroke
CFDA Code
853
DUNS Number
124726725
UEI
GS3YEVSS12N6
Project Start Date
13-September-2024
Project End Date
31-August-2027
Budget Start Date
13-September-2024
Budget End Date
31-August-2027
Project Funding Information for 2024
Total Funding
$1,255,340
Direct Costs
$809,309
Indirect Costs
$446,031
Year
Funding IC
FY Total Cost by IC
2024
NIH Office of the Director
$1,255,340
Year
Funding IC
FY Total Cost by IC
Sub Projects
No Sub Projects information available for 1DP2NS142717-01
Publications
Publications are associated with projects, but cannot be identified with any particular year of the project or fiscal year of funding. This is due to the continuous and cumulative nature of knowledge generation across the life of a project and the sometimes long and variable publishing timeline. Similarly, for multi-component projects, publications are associated with the parent core project and not with individual sub-projects.
No Publications available for 1DP2NS142717-01
Patents
No Patents information available for 1DP2NS142717-01
Outcomes
The Project Outcomes shown here are displayed verbatim as submitted by the Principal Investigator (PI) for this award. Any opinions, findings, and conclusions or recommendations expressed are those of the PI and do not necessarily reflect the views of the National Institutes of Health. NIH has not endorsed the content below.
No Outcomes available for 1DP2NS142717-01
Clinical Studies
No Clinical Studies information available for 1DP2NS142717-01
News and More
Related News Releases
No news release information available for 1DP2NS142717-01
History
No Historical information available for 1DP2NS142717-01
Similar Projects
No Similar Projects information available for 1DP2NS142717-01