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Functional control of electrophysiological network architecture using direct neurostimulation in humans.

Authors :
Khambhati, Ankit N
Khambhati, Ankit N
Kahn, Ari E
Costantini, Julia
Ezzyat, Youssef
Solomon, Ethan A
Gross, Robert E
Jobst, Barbara C
Sheth, Sameer A
Zaghloul, Kareem A
Worrell, Gregory
Seger, Sarah
Lega, Bradley C
Weiss, Shennan
Sperling, Michael R
Gorniak, Richard
Das, Sandhitsu R
Stein, Joel M
Rizzuto, Daniel S
Kahana, Michael J
Lucas, Timothy H
Davis, Kathryn A
Tracy, Joseph I
Bassett, Danielle S
Khambhati, Ankit N
Khambhati, Ankit N
Kahn, Ari E
Costantini, Julia
Ezzyat, Youssef
Solomon, Ethan A
Gross, Robert E
Jobst, Barbara C
Sheth, Sameer A
Zaghloul, Kareem A
Worrell, Gregory
Seger, Sarah
Lega, Bradley C
Weiss, Shennan
Sperling, Michael R
Gorniak, Richard
Das, Sandhitsu R
Stein, Joel M
Rizzuto, Daniel S
Kahana, Michael J
Lucas, Timothy H
Davis, Kathryn A
Tracy, Joseph I
Bassett, Danielle S
Source :
Network neuroscience (Cambridge, Mass.); vol 3, iss 3, 848-877; 2472-1751
Publication Year :
2019

Abstract

Chronically implantable neurostimulation devices are becoming a clinically viable option for treating patients with neurological disease and psychiatric disorders. Neurostimulation offers the ability to probe and manipulate distributed networks of interacting brain areas in dysfunctional circuits. Here, we use tools from network control theory to examine the dynamic reconfiguration of functionally interacting neuronal ensembles during targeted neurostimulation of cortical and subcortical brain structures. By integrating multimodal intracranial recordings and diffusion-weighted imaging from patients with drug-resistant epilepsy, we test hypothesized structural and functional rules that predict altered patterns of synchronized local field potentials. We demonstrate the ability to predictably reconfigure functional interactions depending on stimulation strength and location. Stimulation of areas with structurally weak connections largely modulates the functional hubness of downstream areas and concurrently propels the brain towards more difficult-to-reach dynamical states. By using focal perturbations to bridge large-scale structure, function, and markers of behavior, our findings suggest that stimulation may be tuned to influence different scales of network interactions driving cognition.

Details

Database :
OAIster
Journal :
Network neuroscience (Cambridge, Mass.); vol 3, iss 3, 848-877; 2472-1751
Notes :
application/pdf, Network neuroscience (Cambridge, Mass.) vol 3, iss 3, 848-877 2472-1751
Publication Type :
Electronic Resource
Accession number :
edsoai.on1391582592
Document Type :
Electronic Resource