# Investigating the Role of ACC in the Regulation and Maintenance of Response Inhibition

> **NIH NIH F32** · UNIV OF MARYLAND, COLLEGE PARK · 2021 · $68,562

## Abstract

PROJECT SUMMARY
Dysfunction in the ability to inhibit unwanted responses, response inhibition, is a key component of many
neuropsychiatric disorders. How the brain resolves response conflict remains unclear, but is thought to rely on
several signals including response selection, the detection of conflict and the ability to adapt behavior based on
prior experience. Definitions of these constructs – as we define them – are as follows: ‘Response selection’
signals are tied to the motor system and reflect the nature of the response (e.g., move left or right). When
response selection signals are in conflict with each other (e.g., when neurons that signal leftward and rightward
are simultaneously active), ‘conflict detection’ signals are thought to report the degree of conflict which in turn
allows the development of the correct response selection signal, and activates executive control systems
responsible for conflict adaptation. ‘Conflict adaptation’ refers to the ability to slow behavior after experiencing
an error and/ or a high conflict situation. We have shown that neurons in dorsal medial striatum (DMS) strongly
encode response selections, while neurons in lateral orbitofrontal cortex (OFC) seem to contribute to conflict
adaptation signals. Finally, we have shown that neurons in anterior cingulate cortex (ACC) detect response
conflict prior to the stop change reaction time (SCRT; point at which behavior cannot be inhibited), which is
critical for the resolution of conflict during ongoing behavior. While many studies have suggested that ACC is
important for inhibitory control, few studies have examined whether signals generated by ACC during periods
of high conflict have behaviorally significant effects on downstream regions like DMS and OFC. In AIM 1 we
propose to investigate whether accurate response selections in DMS rely on the conflict detection signals in
ACC. We propose to do this by temporarily silencing neurons in ACC, and examining whether this alters
behavior as well as neural activity in the DMS during response conflict. To further assess this circuit, in a
separate experiment, we propose to optogenetically stimulate neurons in ACC while recording from neurons in
DMS to test whether enhanced conflict detection leads to faster and more accurate response selection. In AIM
2 we propose to investigate the importance of ACC conflict detection in the generation of conflict adaptation
signals in OFC. We predict that disruption of conflict detection in ACC will lead to diminished conflict adaptation
signaling in OFC, and, in a second experiment, that optogenetic stimulation of neurons in the ACC will improve
conflict adaptation signals and enhance behavioral accuracy on high conflict trials. Collectively, these findings
will provide a new perspective on the circuitry supporting response inhibition.

## Key facts

- **NIH application ID:** 10188643
- **Project number:** 5F32MH117836-03
- **Recipient organization:** UNIV OF MARYLAND, COLLEGE PARK
- **Principal Investigator:** Adam T Brockett
- **Activity code:** F32 (R01, R21, SBIR, etc.)
- **Funding institute:** NIH
- **Fiscal year:** 2021
- **Award amount:** $68,562
- **Award type:** 5
- **Project period:** 2019-05-06 → 2022-05-05

## Primary source

NIH RePORTER: https://reporter.nih.gov/project-details/10188643

## Citation

> US National Institutes of Health, RePORTER application 10188643, Investigating the Role of ACC in the Regulation and Maintenance of Response Inhibition (5F32MH117836-03). Retrieved via AI Analytics 2026-05-23 from https://api.ai-analytics.org/grant/nih/10188643. Licensed CC0.

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