# Causal role of delta-beta coupling for goal-directed behavior in anhedonia

> **NIH NIH K99** · UNIV OF NORTH CAROLINA CHAPEL HILL · 2022 · $91,783

## Abstract

PROPOSAL SUMMARY/ABSTRACT
Anhedonia – the inability to seek-out and experience pleasure – is a common symptom in depression that
predicts treatment resistance and is sometimes exacerbated by first-line antidepressants. Anhedonia falls within
the “Positive Valence System” of the Research Domain Criteria framework that comprises two primary
components: “liking” and “wanting.” The “liking,” or consummatory, component reflects the evaluation of rewards
reliant on the medial prefrontal cortex and ventral striatum. The “wanting,” or anticipatory, component modulates
the degree to which effort is expended in goal-directed behavior reliant on the lateral prefrontal cortex and dorsal
striatum. Previous research found decreased neural activity in both of these neural circuits in depressed patients
with anhedonia but has not causally investigated the role of these neural circuits, or their temporal dynamics, in
different components of reward-based decision-making. The preliminary data found decreased goal-directed
behavior in depressed patients with anhedonia and reduced cross-frequency coupling between the phase of
delta oscillations (2-4 Hz) in lateral prefrontal cortex and task-modulated beta oscillations (15-30 Hz) (delta-beta
coupling). The objective of this research plan is to dissect the causal role of frontal-striatal circuity in different
components of reward-based decision-making and their impairment in anhedonia. The central hypothesis is that
anhedonia arises from decreased goal-directed behavior and disruption of delta-beta coupling in lateral prefrontal
cortex and dorsal striatum. The rationale is that spatially and temporally-targeted non-invasive brain stimulation
during performance of a reward-based decision-making task will provide causal evidence for which network
dynamics are impaired in anhedonia. Accordingly, the three specific aims are (1) Causally dissociate the neural
circuits that implement goal-directed behavior and reward-evaluation in decision-making, (2) Increase goal-
directed behavior in depressed patients with anhedonia using network-targeted non-invasive brain stimulation,
and (3) Investigate target engagement of delta-beta coupling in a potential treatment paradigm with network-
targeted stimulation in a randomized clinical trial for depressed patients with symptoms of anhedonia. This
proposal is significant because it will causally evaluate mechanistic models of the networks and cognitive
processes that are disrupted in anhedonia. The work is innovative because it uses concurrent neurophysiology
and neurostimulation, integrates high-resolution spatial and temporal investigation tools, and utilizes
individualized stimulation parameters such as subcortical-targeting with functional-connectivity and task-specific
frequency targeting. The positive impact of this proposal is a refined definition of anhedonia based in biological
mechanism that may have transdiagnostic relevance for other psychiatric illnesses such as schizophre...

## Key facts

- **NIH application ID:** 10488259
- **Project number:** 5K99MH126161-02
- **Recipient organization:** UNIV OF NORTH CAROLINA CHAPEL HILL
- **Principal Investigator:** Justin M Riddle
- **Activity code:** K99 (R01, R21, SBIR, etc.)
- **Funding institute:** NIH
- **Fiscal year:** 2022
- **Award amount:** $91,783
- **Award type:** 5
- **Project period:** 2021-09-13 → 2023-08-31

## Primary source

NIH RePORTER: https://reporter.nih.gov/project-details/10488259

## Citation

> US National Institutes of Health, RePORTER application 10488259, Causal role of delta-beta coupling for goal-directed behavior in anhedonia (5K99MH126161-02). Retrieved via AI Analytics 2026-05-23 from https://api.ai-analytics.org/grant/nih/10488259. Licensed CC0.

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