grant

Effects of DLPFC tDCS on Cognition, Oscillations and GABA Levels in Schizophrenia

Organization UNIVERSITY OF CALIFORNIA-IRVINELocation IRVINE, UNITED STATESPosted 12 Sept 2019Deadline 31 Jul 2026
NIHUS FederalResearch GrantFY2023
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Full Description

PROJECT SUMMARY/ABSTRACT
Cognitive control deficits are associated with poor functioning in schizophrenia (SZ). These deficits include an

impaired ability to maintain task-relevant goals and attention to a task over time, and are connected to impaired

functioning of the dorsolateral prefrontal cortex (DLPFC), a key hub in the neural network supporting cognitive

control. The proposed research uses a non-invasive brain stimulation technique, transcranial direct current

stimulation (tDCS) to test a set of mechanistic hypotheses about the role of the DLPFC in cognitive control

deficits in SZ, focusing on stimulation-induced changes in neural oscillations and DLPFC GABA levels. To do

so, we will use DLPFC-targeted tDCS in combination with electrophysiology (EEG) and magnetic resonance

spectroscopy (MRS) methods to examine stimulation-induced changes in neural activity related to cognitive

control in SZ. Preliminary data from our lab suggests that DLPFC-targeted anodal tDCS can enhance neural

oscillations that support goal maintenance in both healthy controls and individuals with SZ. This

neurostimulation approach offers an exciting new avenue for understanding the neural mechanisms underlying

impaired cognition in SZ, which we propose to utilize with three specific aims. Aim 1: Compare the effects of

task-engaged versus resting tDCS in order to optimize the impact of tDCS on goal maintenance related neural

oscillatory activity and task performance in SZ. Aim 2: Establish the regional specificity of the impact of DLPFC

tDCS (compared to Occipital tDCS) effects on brain circuitry underlying goal maintenance in SZ. Aim 3: Test

hypotheses about relationships between tDCS effects on DLPFC GABA levels, DLPFC-related oscillatory

activity and cognitive performance in SZ. Successful completion of these Aims will address critical gaps in the

literature on cognitive disability in SZ, which has, to date, relied on correlative approaches and will provide new

insights into the role of disrupted DLPFC related brain circuity in SZ and its underlying pathophysiological

mechanisms. It will also provide important new insights into the mechanisms of tDCS effects on brain and

cognition in this illness.

Grant Number: 7R01MH119546-06
NIH Institute/Center: NIH

Principal Investigator: Cameron Carter

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