# κ-opioid receptor: from analgesic target to neuroimmune hub

**Authors:** Qinsi Tan, Mengjin Zheng, Huaixin Xing

PMC · DOI: 10.3389/fphar.2025.1744231 · Frontiers in Pharmacology · 2026-01-07

## TL;DR

The κ-opioid receptor (KOR) is not only involved in pain relief but also plays a key role in regulating the immune system, offering new therapeutic possibilities.

## Contribution

This paper reviews how KOR functions as a neuroimmune hub and explores new drug strategies to harness its benefits while avoiding side effects.

## Key findings

- KOR modulates immune responses by inhibiting pro-inflammatory pathways like NF-κB and STAT3.
- Pharmacological targeting of KOR shows therapeutic potential in immune disorders like multiple sclerosis and atopic dermatitis.
- New drug designs aim to limit central nervous system side effects while preserving KOR's benefits.

## Abstract

Originally characterized as a classical mediator of analgesia, the κ-opioid receptor (KOR) has recently emerged as a pivotal regulator at the crossroads of the nervous and immune systems. Beyond its canonical role in nociceptive processing, a growing body of evidence reveals that KOR exerts profound immunomodulatory effects. The receptor is broadly expressed across diverse immune cell populations, including macrophages, microglia, and lymphocytes, where it contributes to immune homeostasis by attenuating the activity of key pro-inflammatory transcription factors, notably nuclear factor κB (NF-κB) and signal transducer and activator of transcription 3 (STAT3). These regulatory effects are mediated through both canonical G protein–coupled (Gαi/o) pathways and non-canonical β-arrestin–dependent cascades. Preclinical investigations have demonstrated that pharmacological modulation of KOR confers significant therapeutic benefits in a range of immune-related disorders, including atopic dermatitis, multiple sclerosis, and osteoarthritis. However, the clinical translation of traditional KOR agonists remains limited by dose-dependent central nervous system (CNS) adverse effects, such as dysphoria and hallucinations. In this review, we synthesize recent advances in elucidating the molecular and cellular mechanisms underlying KOR-mediated immunoregulation, highlight its therapeutic potential across diverse neuroimmune pathologies, and discuss innovative pharmacological strategies, such as peripherally restricted and signaling-biased ligands-designed to preserve beneficial immunomodulatory and analgesic properties while minimizing CNS liabilities. Collectively, these insights redefine KOR as a central node in neuroimmune communication and point toward the development of next-generation precision therapeutics targeting this axis.

## Linked entities

- **Genes:** OPRK1 (opioid receptor kappa 1) [NCBI Gene 4986], NFKB1 (nuclear factor kappa B subunit 1) [NCBI Gene 4790], STAT3 (signal transducer and activator of transcription 3) [NCBI Gene 6774]
- **Diseases:** atopic dermatitis (MONDO:0004980), multiple sclerosis (MONDO:0005301), osteoarthritis (MONDO:0005178)

## Full-text entities

- **Genes:** NFKB1 (nuclear factor kappa B subunit 1) [NCBI Gene 4790] {aka CVID12, EBP-1, KBF1, NF-kB, NF-kB1, NF-kappa-B1}, OPRK1 (opioid receptor kappa 1) [NCBI Gene 4986] {aka K-OR-1, KOP, KOR, KOR-1, KOR1, OPRK}, STAT3 (signal transducer and activator of transcription 3) [NCBI Gene 6774] {aka ADMIO, ADMIO1, APRF, HIES}, ARRB1 (arrestin beta 1) [NCBI Gene 408] {aka ARB1, ARR1}
- **Diseases:** atopic dermatitis (MESH:D003876), inflammatory (MESH:D007249), multiple sclerosis (MESH:D009103), dysphoria (MESH:D019052), osteoarthritis (MESH:D010003), analgesia (MESH:D000699), hallucinations (MESH:D006212)

## Full text

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## Figures

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## References

99 references — full list in the complete paper: https://tomesphere.com/paper/PMC12819717/full.md

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Source: https://tomesphere.com/paper/PMC12819717