# Limbic glutamatergic circuits in ethanol self-administration

> **NIH NIH P60** · UNIV OF NORTH CAROLINA CHAPEL HILL · 2021 · $267,908

## Abstract

Project Summary/Abstract
Research Component 1. Alcohol addiction is a dynamic multiphasic disorder that is characterized, in part, by
repeated binge/intoxication episodes where the powerful positive reinforcing effects of the drug predominate.
Although multiple neural systems regulate alcohol reinforcement, we have shown that repetitive binge
episodes engage glutamatergic α-amino-3-hydroxy-5-methyl-4-isooxazole receptor (AMPAR) mechanisms of
synaptic plasticity in brain reward pathways. Specifically, binge-like operant alcohol self-administration (SA) is
associated with a shift toward GluA2-lacking Ca2+-permeable (CP-AMPAR) activity (increased GluA1-S831
phosphorylation and reduced GluA2 protein expression) in the basolateral amygdala (BLA). Preliminary
optogenetic data show that these alcohol-induced adaptations are associated with increased AMPAR synaptic
activity in nucleus accumbens core (AcbC) neurons receiving projections from BLA; thus, strongly implicating
the BLAAcbC neural circuit. We have also shown that amygdala AMPAR activity is required for the positive
reinforcing effects of alcohol, and activation of amygdala AMPARs promotes escalated operant alcohol SA.
This convergence of molecular, physiological, and bi-directional behavioral data support the overall hypothesis
that: CP-AMPAR activity in the BLAAcbC pathway functionally regulates the positive reinforcing
effects of alcohol. We propose to test this hypothesis in three separate but integrated aims using male and
female C57Bl/6J mice. First, molecular studies are proposed to evaluate AMPAR subunit protein expression
(GluA1 and GluA2) and phosphorylation (pGluA1-S831 and S845) in amygdala and accumbens subregions to
determine if alcohol SA produces a shift toward GluA2-lacking CP-AMPAR activity in this reward pathway.
Magnetic resonance imaging (MRI) will also be coupled with an optogenetic strategy to identify specific BLA
projections that are altered by alcohol SA. Second, to assess alcohol-induced adaptations in CP-AMPAR
synaptic activity, we will evaluate synaptic properties of BLA neurons projecting to AcbC, and use optogenetics
to test BLAAcbC circuit function in M/F C57BL/6J mice. We predict increased CP-AMPAR signaling in BLA
and BLAAcbC circuit of alcohol SA mice. Third, site-specific pharmacological studies will determine if CP-
AMPAR activity in the BLA or AcbC is necessary for alcohol reinforcement and/or sufficient for escalated
binge-like SA. A site-specific AAV approach will express a dominant negative form of the AMPAR GluA1
subunit (GluA1ct) to determine if activity dependent GluA1 membrane trafficking in the BLA or AcbC regulates
the reinforcing effects of alcohol. These studies will elucidate novel molecular mechanism(s) of alcohol’s
reinforcing effects, which has potential to lead to new therapeutic strategies for treating behavioral pathologies
associated with alcohol addiction. The overall goal of the UNC ARC is to increase understanding of molecular
and c...

## Key facts

- **NIH application ID:** 10078815
- **Project number:** 5P60AA011605-24
- **Recipient organization:** UNIV OF NORTH CAROLINA CHAPEL HILL
- **Principal Investigator:** Clyde W Hodge
- **Activity code:** P60 (R01, R21, SBIR, etc.)
- **Funding institute:** NIH
- **Fiscal year:** 2021
- **Award amount:** $267,908
- **Award type:** 5
- **Project period:** — → —

## Primary source

NIH RePORTER: https://reporter.nih.gov/project-details/10078815

## Citation

> US National Institutes of Health, RePORTER application 10078815, Limbic glutamatergic circuits in ethanol self-administration (5P60AA011605-24). Retrieved via AI Analytics 2026-05-22 from https://api.ai-analytics.org/grant/nih/10078815. Licensed CC0.

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