# Inhibition of mast cell activation by Jaranol-targeted Pirin ameliorates allergic responses in mouse allergic rhinitis

**Authors:** Yue Huang, Shuhua Su, Bo Duan, Yunfei Zhang, Zhengmin Xu

PMC · DOI: 10.1515/biol-2022-1030 · Open Life Sciences · 2025-03-28

## TL;DR

Jaranol, a compound from traditional herbs, reduces allergic rhinitis by inhibiting mast cell activity and inflammation in mice.

## Contribution

Jaranol's anti-inflammatory mechanism involves targeting Pirin to suppress mast cell function in allergic responses.

## Key findings

- Jaranol reduced nasal inflammation and mast cell numbers in an allergic rhinitis mouse model.
- Jaranol inhibited secretion of multiple inflammatory cytokines from mast cells.
- Jaranol suppressed mast cell proliferation, migration, and function by targeting Pirin expression.

## Abstract

Jaranol, a bioactive compound derived from various traditional medicinal herbs, has demonstrated significant anti-inflammatory properties. This study investigates its effects and possible mechanisms underlying its anti-inflammatory role in mast cells, as well as ovalbumin (OVA)-induced allergic rhinitis (AR) mice model. Forty mice were randomly divided into blank, AR, dexamethasone (positive control), and Jaranol groups (10 mg/ml), with 10 mice in each group. Jaranol was found to inhibit nasal mucosal inflammation and reduce mast cell numbers in AR models. It also inhibited the secretion of several inflammatory cytokines (IFN-γ, TNF-α, IL-1β, IL-6, MCP-1, and CXCR10) from mast cells, as well as mast cell proliferation and migration. Interestingly, Pirin was differentially expressed in blank, AR, and Jaranol groups. Further studies indicated that Jaranol inhibited inflammatory cytokine secretion from mast cells by mediating Pirin and also inhibited mast cell proliferation and migration. Moreover, it inhibited mast cell function by suppressing Pirin expression. These findings suggest that Jaranol exerts its therapeutic effects by inhibiting Pirin expression in mast cells, thereby reducing inflammation and histopathological changes associated with AR.

## Linked entities

- **Genes:** PRN (pirin) [NCBI Gene 825091]
- **Proteins:** IFNG (interferon gamma), TNF (tumor necrosis factor), IL1B (interleukin 1 beta), IL6 (interleukin 6), CCL2 (C-C motif chemokine ligand 2), LOC123027491 (C-X-C chemokine receptor type 2-like)
- **Chemicals:** Jaranol (PubChem CID 5318869), dexamethasone (PubChem CID 5743)
- **Diseases:** allergic rhinitis (MONDO:0011786)
- **Species:** Mus musculus (taxon 10090)

## Full-text entities

- **Genes:** Tnf (tumor necrosis factor) [NCBI Gene 21926] {aka DIF, TNF-a, TNF-alpha, TNFSF2, TNFalpha, Tnfa}, Il6 (interleukin 6) [NCBI Gene 16193] {aka Il-6}, Il1b (interleukin 1 beta) [NCBI Gene 16176] {aka IL-1beta, Il-1b}, Pir (pirin) [NCBI Gene 69656] {aka 2310042L19Rik, Pirnl}, Ifng (interferon gamma) [NCBI Gene 15978] {aka IFN-g, If2f, Ifg}, Serpinb1-ps1 (serine (or cysteine) peptidase inhibitor, clade B, member 1, pseudogene) [NCBI Gene 282665] {aka EID, ovalbumin}
- **Diseases:** inflammatory cytokines (MESH:D000080424), inflammation (MESH:D007249), AR (MESH:D065631)
- **Chemicals:** Jaranol (-), dexamethasone (MESH:D003907)
- **Species:** Mus musculus (house mouse, species) [taxon 10090]

## Full text

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## Figures

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Source: https://tomesphere.com/paper/PMC11964180