Voltage Imaging Analysis of Striatal Network Dynamics Related to Movement, Parkinson's Disease and Deep Brain Stimulation
Project Number3R01NS115797-05S1
Contact PI/Project LeaderHAN, XUE
Awardee OrganizationBOSTON UNIVERSITY (CHARLES RIVER CAMPUS)
Description
Abstract Text
Title: Voltage imaging analysis of striatal network dynamics related to movement, Parkinson’s disease
and deep brain stimulation
Summary
Deep brain stimulation (DBS) delivers high frequency electrical current stimulation through chronically
implanted electrodes. DBS has been FDA approved for managing several brain disorders, including Parkinson’s
disease (PD), epilepsy, essential tremor, and obsessive compulsive disorders. However, the therapeutic
mechanisms of DBS remain largely unknown. There are many intriguing hypothesis, but experimental evidence
has been limited. The increasing use of DBS for PD over the past 20 years has offered a unique opportunity to
record from various basal ganglia brain structures in patients, and accumulating evidence suggests that
exaggerated pathological local field potential (LFP) beta oscillations (~10-30Hz) in the cortical-basal ganglia
circuit are a signature of PD. Using exaggerated LFP beta oscillations recorded in STN as a target feature, a
recent study showed that closed-loop DBS could be more effective in alleviating akinesia in primate PD models,
highlighting the potential of using pathological beta oscillations as a biomarker for PD.
PD is characterized by degeneration of SNpc dopamine neurons that project to the striatum. The fact that
DBS is effective at managing motor pathologies highlights that PD involves neural circuit deficits that can be
altered by electrical stimulation to achieve therapeutic effects. The central goal of this proposal is to study the
neural circuit dynamics related to PD, and the therapeutic mechanisms of DBS, using a novel single cell voltage
imaging technique that was recently developed in Dr. Han’s lab. Specifically, we will examine how individual
striatal neurons’ subthreshold membrane voltage and spiking patterns relate to bulk striatal LFP oscillations
during voluntary movement in healthy and dopamine-depleted PD conditions, and how DBS alters these
interactions. Such understanding will provide important insights into the relationship between individual neurons
subthreshold membrane voltage dynamics (a measure of synaptic inputs) and spiking outputs, and provide direct
experimental evidence linking pathological LFP oscillations with single neuron biophysics, and how DBS affects
these relationships. We believe that such insights will help establish oscillation based biomarkers for brain
disorders, and facilitate future DBS designs.
Public Health Relevance Statement
Project Narrative
Deep brain stimulation (DBS) has been FDA approved for managing several brain disorders, including
Parkinson’s disease (PD), and has been increasingly used to treat patient over the past couple decades.
However, the therapeutic mechanisms of DBS remain largely unknown. This study aims to systematically study
the neural circuits involved in PD, and the therapeutic mechanisms of DBS using novel single cell voltage
imaging techniques.
National Institute of Neurological Disorders and Stroke
CFDA Code
853
DUNS Number
049435266
UEI
THL6A6JLE1S7
Project Start Date
01-April-2020
Project End Date
31-March-2026
Budget Start Date
01-April-2024
Budget End Date
31-March-2026
Project Funding Information for 2024
Total Funding
$89,789
Direct Costs
$57,760
Indirect Costs
$32,029
Year
Funding IC
FY Total Cost by IC
2024
National Institute of Neurological Disorders and Stroke
$89,789
Year
Funding IC
FY Total Cost by IC
Sub Projects
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