# Gastrin-releasing peptide signaling in the nucleus accumbens medial shell regulates neuronal excitability and motivation

**Authors:** Erin E. Aisenberg, Thomas L. Li, Hongli Wang, Atehsa A. Sahagun, Emilie M. Tu, Helen S. Bateup

PMC · DOI: 10.1038/s41467-025-64373-3 · Nature Communications · 2025-10-21

## TL;DR

This study shows that gastrin-releasing peptide signaling in a brain region called the nucleus accumbens affects neuron activity and motivation in mice.

## Contribution

The novel finding is that GRP signaling in the nucleus accumbens medial shell regulates neuronal excitability and motivation.

## Key findings

- GRP receptor is expressed in nucleus accumbens medial shell neurons targeted by VTA, hippocampus, and amygdala.
- NAc GRPR-positive cells include D2 receptor-expressing neurons with high intrinsic excitability.
- Deleting Grpr in the NAc increases motivation in mice, showing GRPR's role in regulating motivated behavior.

## Abstract

Neuropeptides are the largest class of neuromodulators. It has been shown that subpopulations of ventral tegmental area (VTA) dopamine neurons express mRNA for the neuropeptide Gastrin-releasing peptide (GRP); however, its functional relevance in mesolimbic circuits is unknown. Here we report that the GRP receptor (GRPR) is expressed in nucleus accumbens medial shell (NAc MSh) neurons, which are targeted by GRP-expressing inputs from the VTA, hippocampus, and amygdala. We show that NAc MSh GRPR-positive cells represent subpopulations of D2 receptor-expressing neurons, comprising both classical striatal projection neurons (SPNs) and eccentric SPNs. GRPR-expressing neurons have high intrinsic excitability and can be activated by GRP in vivo. NAc-specific deletion of Grpr in mice increases motivation in a progressive ratio test, demonstrating that GRPR regulates motivated behaviors. These experiments establish GRP/GRPR signaling as a potent modulator of mesolimbic circuits and advance our understanding of the diversity of cell types present in the NAc.

The nucleus accumbens (NAc) controls reward learning and motivated behaviors. Here, authors show that the neuropeptide gastrin-releasing peptide regulates the excitability of subpopulations of NAc neurons and modulates motivated behavior in mice.

## Linked entities

- **Genes:** GRPR (gastrin releasing peptide receptor) [NCBI Gene 2925]
- **Proteins:** GRP (gastrin releasing peptide), GRPR (gastrin releasing peptide receptor), DIO2 (iodothyronine deiodinase 2)
- **Species:** Mus musculus (taxon 10090)

## Full-text entities

- **Genes:** Grpr (gastrin releasing peptide receptor) [NCBI Gene 14829] {aka GRP-R}, Grp (gastrin releasing peptide) [NCBI Gene 225642] {aka BLP}, Drd2 (dopamine receptor D2) [NCBI Gene 13489] {aka D2R, Drd-2}
- **Chemicals:** dopamine (MESH:D004298)
- **Species:** Mus musculus (house mouse, species) [taxon 10090]

## Full text

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## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12540653/full.md

## References

6 references — full list in the complete paper: https://tomesphere.com/paper/PMC12540653/full.md

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Source: https://tomesphere.com/paper/PMC12540653