# Receptor variant-based changes in the role of PACAP in the nucleus accumbens during the transition to ethanol dependence

> **NIH NIH F31** · DREXEL UNIVERSITY · 2024 · $48,974

## Abstract

PROJECT SUMMARY
Stress-related systems undergo a change during the transition to ethanol dependence, such that activation,
which in a non-dependent state may leave unaffected or suppress intake, instead increases consumption. This
effect reversal often coincides with an upregulation in receptor gene expression for stress-related neuropeptides;
however, for the stress-related neuropeptide, pituitary adenylate cyclase-activating polypeptide (PACAP), the
changes instead appear to occur via a specific increase in receptor variant expression. Our study focuses
attention on the paraventricular nucleus of the thalamus (PVT), which has notably and selectively dense
expression of the less ubiquitous PACAP peptide isoform, PACAP-27, where it is expressed in a subpopulation
of glutamatergic neurons. In preliminary studies, we have found with a 20% ethanol intermittent access (IA)
model of binge drinking, that effects of PACAP+ cell manipulation in the PVT can change based on drinking
history. In PACAP-Cre mice drinking under the IA model for 6 weeks, Cre-dependent chemogenetic inhibition of
PACAP+ cells stimulated ethanol drinking in low drinkers but instead inhibited intake in high drinkers. With
preliminary evidence that these PACAP-27+ PVT neurons send dense projections to the nucleus accumbens
(NAc), we have also found in rats, which drink lower levels of ethanol than mice, that those drinking under the
IA model for 6 weeks respond to PACAP-27 injection into the NAc with a suppression of ethanol intake. Further,
rats with a longer IA drinking history (10 weeks) show a specific increase in gene expression in the NAc of the
HOP variant of the PACAP receptor (PAC1). We have confirmed with quantitative real-time (qRT-)PCR that the
HOP and SHORT variants are present in the NAc of mice. Building on our preliminary and published data, we
hypothesize that activation of PACAP-27+ cells that send afferents from the PVT to the NAc suppresses non-
dependent, binge-like ethanol intake, but increases intake in a dependent state (Aim 1); and this shift in
behavioral output occurs as the PACAP system becomes dysregulated resulting in a specific increase in PAC1
HOP receptor variant expression (Aim 2). To test this, Aim 1 investigates the effect of activation and inhibition
of the PVT→NAc PACAP pathway on ethanol intake before and after dependence, by using PACAP-Cre mice
and Cre-dependent excitatory and inhibitory DREADDs injected into the PVT paired with cannula guided
microinjections of CNO into the NAc shell. To determine the involvement of PAC1 receptor variants in the NAc
on ethanol intake, Aim 2 will measure PAC1 variant mRNA expression in the NAc of non-dependent and ethanol
dependent mice and also use specific interfering (si)RNA to knock down the PAC1 receptor variants in the NAc
of non-dependent and dependent mice. Together, these Aims will determine how the PACAP+ PVT→NAc
pathway affects ethanol drinking across states and how PAC1 variant populations in the ...

## Key facts

- **NIH application ID:** 10928161
- **Project number:** 5F31AA031427-02
- **Recipient organization:** DREXEL UNIVERSITY
- **Principal Investigator:** Brody Allen Carpenter
- **Activity code:** F31 (R01, R21, SBIR, etc.)
- **Funding institute:** NIH
- **Fiscal year:** 2024
- **Award amount:** $48,974
- **Award type:** 5
- **Project period:** 2023-09-01 → 2026-08-31

## Primary source

NIH RePORTER: https://reporter.nih.gov/project-details/10928161

## Citation

> US National Institutes of Health, RePORTER application 10928161, Receptor variant-based changes in the role of PACAP in the nucleus accumbens during the transition to ethanol dependence (5F31AA031427-02). Retrieved via AI Analytics 2026-05-26 from https://api.ai-analytics.org/grant/nih/10928161. Licensed CC0.

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