# Higher levels of D2R and D3R in the frontal–striatal regions are associated with reduced perseverative reward seeking after opioid abstinence

**Authors:** Yingying Li, Xigeng Zheng, Cong Gao, Shao Li, Zhengkui Liu, Meixuan Lv, Fei Xiao, Yunjing Bai

PMC · DOI: 10.3389/fnbeh.2025.1552055 · Frontiers in Behavioral Neuroscience · 2025-06-02

## TL;DR

Higher dopamine receptor levels in certain brain regions may help reduce reward-seeking behaviors after opioid abstinence.

## Contribution

This study reveals how D2R and D3R levels in frontal-striatal regions correlate with reduced perseverative reward seeking after opioid use.

## Key findings

- Morphine-treated rats with high D2R in the ventral striatum showed lower approaching behaviors.
- D3R levels in the dorsal striatum differed between high- and low-responding morphine-treated rats.
- D3R levels in the mPFC showed an inverted U-shaped relationship with reward-seeking behaviors.

## Abstract

The lower levels of dopamine D2 receptor (D2R) in the striatum and the heightened levels of dopamine D2 receptor (D3R) in the midbrain have been linked to impulsive behavior and risky decision-making associated with drug dependence. While D3R has been considered a potential target for treating drug dependence, the connection between D3R in the prefrontal-striatal regions and maladaptive drug-related behaviors remains poorly understood.

This study utilized two high-cost tasks to investigate perseverative reward seeking, specifically conflict-based approaching behavior and persistent responding behavior under a progesterone receptor (PR) procedure. Additionally, D2R and D3R levels in the medial prefrontal cortex (mPFC) and striatum were examined through Western blotting.

After each task, male rats were divided into two subpopulations: high-approaching vs. low-approaching and high-responding vs. low-responding. Rats treated with morphine (MOR) exhibited a 3 fold increase in the likelihood of developing high-approaching or high-responding behaviors compared to drug-naïve rats. D2R expression was higher in the ventral striatum of morphine-treated, low-approaching rats than high-approaching rats, negatively correlating with approaching behaviors within the morphine-exposed group. After six consecutive PR sessions, D3R levels in the dorsal striatum differed significantly between morphine-treated, low-responding rats and morphine-treated, high-responding rats, negatively correlating with responding behaviors within the morphine-exposed group. An intriguing finding was the non-linear relationships, resembling an inverted U shape, observed between the level of D3R in the mPFC and reward-seeking behaviors, as revealed by both tasks.

The elevated or relatively higher levels of D2R and D3R in the frontal-striatal regions may serve as protective factors for individuals abstaining from opioids, enabling them to control their reward-seeking behavior better.

## Linked entities

- **Proteins:** DRD2 (dopamine receptor D2), D3R (temporal expression: late), PGR (progesterone receptor)
- **Chemicals:** morphine (PubChem CID 5288826)
- **Species:** Rattus norvegicus (taxon 10116)

## Full-text entities

- **Genes:** Pgr (progesterone receptor) [NCBI Gene 25154]
- **Diseases:** drug dependence (MESH:D019966), impulsive behavior (MESH:D010554)
- **Chemicals:** MOR (MESH:D009020)
- **Species:** Rattus norvegicus (brown rat, species) [taxon 10116]

## Full text

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## Figures

11 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12171296/full.md

## References

109 references — full list in the complete paper: https://tomesphere.com/paper/PMC12171296/full.md

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Source: https://tomesphere.com/paper/PMC12171296