Central thalamic deep brain stimulation (CT-DBS) is a promising therapy for restoring consciousness in patients in coma and vegetative state by changing the arousal state. Early experimental studies have established a causal link between central thalamus electrical brain stimulation and forebrain arousal. Clinical investigators in the 1960s and 1970s considered the potential relevance of the findings as a method for restoration of arousal and consciousness in chronically unconscious patients and carried out pilot case studies of electrical stimulation. However, despite eye opening and autonomic signs consistent with arousal effects, no reports described sustained recovery of interactive behavior. Following on these early case reports, a multicenter study involving a total of 49 patients was carried out. Deep brain stimulation resulted in increases in arousal and associated physiological responses in the majority of these patients but there were unfortunately no changes in behavioral responsiveness. More recently, a single subject study provided the first compelling evidence that some severely brain injured patients in minimally conscious state (MCS) may benefit from CT/DBS. The overall findings indicated significantly improved behavioral responsiveness with a combination of immediate as well as slowly accumulating, though long-lasting effects. However, this type of response has only been observed in a single subject and has been difficult to reproduce. While these earlier findings raise the possibility that using CT/DBS to improve consciousness in severe traumatic brain injury could be efficacious, many critical challenges lay ahead. These include defining the mechanisms of action and optimizing stimulation targets and parameters to make CT/DBS a reliable clinical treatment. In this proposal, we aim to overcome these challenges. We will develop and utilize a novel optogenetic functional magnetic resonance imaging approach that will enable us to systematically understand the underlying mechanism of action of the CT/DBS therapy with unparalleled clarity. Elucidating the mechanism of CT-DBS therapy will allow us to optimize the stimulation target, stimulation parameters, and even help stratify patients for inclusion into such therapeutic modalities. In Preliminary Studies we have established the effectiveness of the ofMRI approach at identifying key locations of stimulation and, importantly, function associated with CT-DBS. We will first conduct ofMRI, EEG, and behavioral studies in normal animals to define circuit mechanisms involved in both acute and long-term stimulation. Then, we will evaluate the optimized parameters of stimulation and their role in restoring consciousness in animal models of TBI. Knowledge of CT-DBS mechanism and optimization parameters will be invaluable for future clinical trials, understanding of mechanisms of arousal, consciousness, and neuromodulation therapy.

Public Health Relevance

Electrical brain stimulation is an important new treatment for traumatic brain injury patients that have long-term loss of consciousness, but benefit is limited due to lack of mechanistic understanding. Utilizing a novel technology that enables specific brain cells to be selectively modulated with precision while their signal pathways are visualized, we will develop new ways to understand mechanisms of brain stimulation therapy. Utilizing this method, we will identify the sweet spot for the brain stimulation therapy to be most effective at restoring consciousness.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Research Project (R01)
Project #
5R01NS087159-03
Application #
9146417
Study Section
Acute Neural Injury and Epilepsy Study Section (ANIE)
Program Officer
He, Janet
Project Start
2014-09-30
Project End
2019-08-31
Budget Start
2016-09-01
Budget End
2017-08-31
Support Year
3
Fiscal Year
2016
Total Cost
$375,620
Indirect Cost
$156,870
Name
Stanford University
Department
Neurosurgery
Type
Schools of Medicine
DUNS #
009214214
City
Stanford
State
CA
Country
United States
Zip Code
94304
Asaad, Mazen; Lee, Jin Hyung (2018) A guide to using functional magnetic resonance imaging to study Alzheimer's disease in animal models. Dis Model Mech 11:
Lee, Jin Hyung; Kreitzer, Anatol C; Singer, Annabelle C et al. (2017) Illuminating Neural Circuits: From Molecules to MRI. J Neurosci 37:10817-10825
Choy, ManKin; Duffy, Ben A; Lee, Jin Hyung (2017) Optogenetic study of networks in epilepsy. J Neurosci Res 95:2325-2335
Liu, Jia; Duffy, Ben A; Bernal-Casas, David et al. (2017) Comparison of fMRI analysis methods for heterogeneous BOLD responses in block design studies. Neuroimage 147:390-408
Bernal-Casas, David; Lee, Hyun Joo; Weitz, Andrew J et al. (2017) Studying Brain Circuit Function with Dynamic Causal Modeling for Optogenetic fMRI. Neuron 93:522-532.e5
Fang, Zhongnan; Van Le, Nguyen; Choy, ManKin et al. (2016) High spatial resolution compressed sensing (HSPARSE) functional MRI. Magn Reson Med 76:440-55
Duffy, Ben A; Choy, ManKin; Chuapoco, Miguel R et al. (2015) MRI compatible optrodes for simultaneous LFP and optogenetic fMRI investigation of seizure-like afterdischarges. Neuroimage 123:173-84
Liu, Jia; Lee, Hyun Joo; Weitz, Andrew J et al. (2015) Frequency-selective control of cortical and subcortical networks by central thalamus. Elife 4:e09215
Duffy, Ben A; Weitz, Andrew J; Lee, Jin Hyung (2014) In vivo imaging of transplanted stem cells in the central nervous system. Curr Opin Genet Dev 28:83-8