Award Abstract # 1264535
Collaborative research: Optimal stimulus waveform design for Parkinson's disease

NSF Org: CBET
Division of Chemical, Bioengineering, Environmental, and Transport Systems
Recipient: UNIVERSITY OF CALIFORNIA, SANTA BARBARA
Initial Amendment Date: August 8, 2013
Latest Amendment Date: August 24, 2016
Award Number: 1264535
Award Instrument: Standard Grant
Program Manager: Michele Grimm
CBET
 Division of Chemical, Bioengineering, Environmental, and Transport Systems
ENG
 Directorate for Engineering
Start Date: August 15, 2013
End Date: July 31, 2017 (Estimated)
Total Intended Award Amount: $215,889.00
Total Awarded Amount to Date: $259,065.00
Funds Obligated to Date: FY 2013 = $215,889.00
FY 2016 = $43,176.00
History of Investigator:
  • Jeffrey Moehlis (Principal Investigator)
    moehlis@engineering.ucsb.edu
Recipient Sponsored Research Office: University of California-Santa Barbara
3227 CHEADLE HALL
SANTA BARBARA
CA  US  93106-0001
(805)893-4188
Sponsor Congressional District: 24
Primary Place of Performance: University of California-Santa Barbara
Office of Research, 3227 Cheadle
Santa Barbara
CA  US  93106-2050
Primary Place of Performance
Congressional District:
24
Unique Entity Identifier (UEI): G9QBQDH39DF4
Parent UEI:
NSF Program(s): Disability & Rehab Engineering,
IntgStrat Undst Neurl&Cogn Sys
Primary Program Source: 01001314DB NSF RESEARCH & RELATED ACTIVIT
01001617DB NSF RESEARCH & RELATED ACTIVIT
Program Reference Code(s): 8091, 8551, 8089, 010E
Program Element Code(s): 534200, 862400
Award Agency Code: 4900
Fund Agency Code: 4900
Assistance Listing Number(s): 47.041

ABSTRACT

PI: Netoff, Theoden I. and Moehlis, Jeffrey M.
Proposal Number: 1264432 & 1264535

Intellectual Merit: Populations of neurons must dynamically synchronize and desynchronize for transmission of information within the brain. The disruption of this dynamic synchronization is thought to underlie the symptomatology of several neurological disorders. Deep Brain Stimulation (DBS) therapy is being used to treat many of these neurological disorders, such as Parkinsons disease (PD). It is generally believed that DBS leads are placed in regions of brain that are pathologically synchronous, and periodic DBS pulses then "over pace" these areas, blocking the pathological activity. The PIs have recently developed an alternative hypothesis for the mechanism of DBS which focuses on DBS's modulation of the firing times of neurons. Stimulation at certain frequencies can induce a chaotic response that desynchronizes a population; we term this chaotic desynchronization. The response of a neuron to a DBS pulse is characterized by its phase response curve (PRC), a measure of how the stimulus advances the phase depending on the phase the stimulus is applied at. The PRC can then be used to determine if two neurons in the population starting at nearly the same phase will entrain to the stimulus pulses, or will diverge and effectively become desynchronized. In this grant the PIS propose to use PRCs to determine the optimal stimuli to desynchronize population oscillations. Preliminary experiments show that small periodic stimulus pulses at certain frequencies can desynchronize populations; the frequency and amplitude that desynchronize can be predicted from the PRC of the neurons to the stimulus. Moreover, continuous stimulus waveforms can be designed that desynchronize populations with much less energy than the pulsatile stimuli. The aims of this grant are to further the theoretical work in designing these waveforms from measured PRCs, and then to test chaotic de-synchronization in physical and biological systems. Specific Aim 1 will use measured phase response curves and control theory to determine the optimal stimulus waveforms to maximize desynchronization of neuronal ensembles. Specific Aim 2 will be to apply this theory to desynchronize oscillations in a chemical oscillator model, the photosensitive Belousov-Zhabotinsky (pBZ) reaction, through pulsatile and continuous waveform photo stimulation. Specific Aim 3 will test the theory in neurons in vitro basal ganglia preparation. Neurons will be recorded and stimulated using a dynamic clamp experimental protocol. The PRCs from single neurons will be measured in response to DBS pulses, and we will test for chaotic behavior in their stimulus response patterns.

Broader Impacts: The motivation of this research is to 1) understand how behaviors relate to oscillatory synchronization in and between the basal ganglia and motor cortex, and 2) improve DBS treatment of PD, for which the selection of stimulus electrodes, frequency, and amplitudes are currently tuned manually by a clinician. The goal of this research is to determine the optimal stimulus properties based on simple physiological measures of the neurophysiological response to DBS. This approach will enable faster and more robust programming of neurostimulators and will decrease the amount of required injected current, which will reduce side effects and battery power consumption. This approach has high potential for closed loop control algorithms where DBS parameters are automatically tuned to maintain maximal efficacy. This approach may also be applied to seizure suppression and other neurological diseases. These studies leverage a recently funded IGERT training plan at UMN for neuromodulation. To maximize our clinical impact, we have discussed with Dwight Nelson (Neuromodulation department at Medtronic) what basic research will enable the next steps in developing new DBS stimulus parameters and the yet unmet clinical needs (letter of support included). The results from this research will be disseminated to the public through various education programs including ones focused on underrepresented undergraduate students, high school educators, high school students and junior-high school students. Finally, this award will train graduate students and undergraduates in interdisciplinary research activities, and enhance the education of other graduate students through results that will be incorporated into courses taught by the PI and co-PI.

PUBLICATIONS PRODUCED AS A RESULT OF THIS RESEARCH

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(Showing: 1 - 10 of 15)
A.B. Holt, D. Wilson, M. Shinn, J. Moehlis, T.I. Netoff "Phasic burst stimulation: a closed-loop approach to tuning deep brain stimulation parameters for Parkinson's disease" PLOS Computational Biology , v.13 , 2016 , p.e1005011
A.B. Holt, T.I. Netoff "Origins and suppression of oscillations in a computational model of Parkinson's disease" J. Computational Neuroscience , v.37 , 2014 , p.505
A.T. Connolly, A.L. Jensen, E.M. Bello, T.I. Netoff, K.B. Baker, M.D. Johnson, J.L. Vitek "Modulators in oscillatory frequency and coupling in globus pallidus with increasing parkinsonian severity" J. Neuroscience , v.35 , 2015 , p.6231
Dan Wilson and Jeff Moehlis "Locally optimal extracellular stimulation for chaotic desynchronization of neural populations" Journal of Computational Neuroscience , v.37 , 2014 , p.243
D. Wilson, A.B. Holt, T.I. Netoff, J. Moehlis "Optimal entrainment of heterogeneous noisy neurons" Frontiers in Neuroscience , v.9 , 2015 , p.192
D. Wilson and J. Moehlis "Analytical bounds on the critical coupling strength in a population of heterogeneous biological oscillators" Proceedings of the 2016 American Control Conference , 2016 , p.5772
D. Wilson and J. Moehlis "An energy-optimal approach for entrainment of uncertain circadian oscillators" Biophysical Journal , v.107 , 2014 , p.1744
D. Wilson and J. Moehlis "Clustered desynchronization from high-frequency deep brain stimulation" PLOS Computational Biology , v.11 , 2015 , p.e1004673
D. Wilson and J. Moehlis "Determining individual phase response curves from aggregate population data" Physical Review E , v.92 , 2015 , p.022902
D. Wilson and J. Moehlis "Isostable reduction of periodic orbits" Physical Review E , v.94 , 2016 , p.052213
D. Wilson and J. Moehlis "Isostable reduction with applications to time-depenent partial differential equations" Physical Review E , v.94 , 2016 , p.012211
(Showing: 1 - 10 of 15)

PROJECT OUTCOMES REPORT

Disclaimer

This Project Outcomes Report for the General Public is displayed verbatim as submitted by the Principal Investigator (PI) for this award. Any opinions, findings, and conclusions or recommendations expressed in this Report are those of the PI and do not necessarily reflect the views of the National Science Foundation; NSF has not approved or endorsed its content.

 

The brain is an amazing organ which is responsible for a number of important functions including cognition, attention, emotion, perception, memory, and motor control.  Certain neurological diseases are associated with pathological brain activity.  For example, it has been hypothesized that some symptoms of Parkinson's disease are caused by pathologically synchronized neural activity in the motor control region of the brain.

With this in mind, we have developed novel methods for designing electrical deep brain stimulation inputs which desynchronize the activity of a group of neurons.  These methods use data on the response properties of neurons to stimulation pulses, which can be obtained from mathematical models or experimentally.  We have demonstrated the effectiveness of these methods using computer simulations, and experimentally both for in vitro neurons and for a network of chemical oscillators which behaves in a similar fashion.  Notably, our methods require less energy than existing deep brain stimulation approaches, which could allow the battery which provides the power for deep brain stimulation to last longer, reducing the need for battery replacement surgery which is expensive and has risks of complications.

This work represents an important step toward the ultimate goal of designing the first deep brain stimulator for treatment of Parkinson's disease which automatically tunes its electrical stimuli in order to optimize treatment effectiveness.


Last Modified: 12/27/2017
Modified by: Jeffrey M Moehlis

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