# In Vitro Evaluation of the Inhibitory Effects of Linarin on Histamine‐Induced Expression of Proinflammatory Cytokines, Mucin 5AC, and Aquaporin 5 in Human Nasal and Bronchial Epithelial Cells

**Authors:** Xin‐Jing Mi, Jie Wang, Jian‐Qiang Qi

PMC · DOI: 10.1002/kjm2.70114 · The Kaohsiung Journal of Medical Sciences · 2025-09-25

## TL;DR

This study shows that linarin, a plant compound, can reduce inflammation and mucus production in cells related to allergic rhinitis and asthma.

## Contribution

The study demonstrates linarin's inhibitory effects on histamine-induced inflammation and mucus changes in nasal and bronchial cells.

## Key findings

- Linarin reduced histamine-induced expression of proinflammatory cytokines like IL-6, IL-8, and MCP-1.
- Linarin reversed histamine-induced MUC5AC upregulation and AQP5 downregulation in epithelial cells.
- Linarin inhibited NF-κB and MAPK pathways, which are key in inflammatory responses.

## Abstract

Allergic rhinitis and asthma are two prevalent chronic allergic conditions in children. Linarin, a glycosylated flavonoid derived from various plants, exhibits a wide range of biological activities. This study aimed to investigate the therapeutic potential of linarin against allergic rhinitis and asthma. In vitro models of allergic rhinitis and asthma were established using human nasal epithelial cells (hNECs) and human bronchial epithelial cells (BEAS‐2B), respectively. Linarin treatment inhibited histamine‐induced increases in the expression levels of p‐p65 and p‐IκBα in whole‐cell lysates, as well as p65 in nuclear lysates. The histamine‐induced activation of MAPK pathways was suppressed by linarin, as evidenced by reduced phosphorylation ratios of ERK (pERK/ERK), JNK (pJNK/JNK), and p38 (pp38/p38). ELISA results further revealed that linarin attenuated histamine‐induced secretion of proinflammatory cytokines, including IL‐6, IL‐8, and MCP‐1. Western blot and RT‐PCR analyses showed that linarin reversed histamine‐induced MUC5AC upregulation and AQP5 downregulation. Notably, the inhibitory effects of linarin were potentiated in the presence of specific inhibitors targeting NF‐κB (PDTC), ERK (U0126), p38 (SB203580), and JNK (SP600125). Collectively, these findings demonstrate that linarin suppresses histamine‐induced proinflammatory cytokine secretion, MUC5AC upregulation, and AQP5 downregulation in human nasal and bronchial epithelial cells. These effects are mediated through the inhibition of the NF‐κB and MAPK pathways. Thus, linarin may serve as a promising therapeutic agent for the treatment of allergic rhinitis and asthma.

## Linked entities

- **Genes:** Lcp1 (lymphocyte cytosolic protein 1) [NCBI Gene 18826], RELA (RELA proto-oncogene, NF-kB subunit) [NCBI Gene 5970], EPHB2 (EPH receptor B2) [NCBI Gene 2048], MAPK8 (mitogen-activated protein kinase 8) [NCBI Gene 5599], CRK (CRK proto-oncogene, adaptor protein) [NCBI Gene 1398], MUC5AC (mucin 5AC, oligomeric mucus/gel-forming) [NCBI Gene 4586], AQP5 (aquaporin 5) [NCBI Gene 362]
- **Chemicals:** Linarin (PubChem CID 5317025), histamine (PubChem CID 774), PDTC (PubChem CID 10176668), U0126 (PubChem CID 3006531), SB203580 (PubChem CID 176155), SP600125 (PubChem CID 8515), IL-6 (PubChem CID 165368475), IL-8 (PubChem CID 169410440)
- **Diseases:** allergic rhinitis (MONDO:0011786), asthma (MONDO:0004979)
- **Species:** Homo sapiens (taxon 9606)

## Full-text entities

- **Genes:** MAPK8 (mitogen-activated protein kinase 8) [NCBI Gene 5599] {aka JNK, JNK-46, JNK1, JNK1A2, JNK21B1/2, PRKM8}, NFKBIA (NFKB inhibitor alpha) [NCBI Gene 4792] {aka EDAID2, IKBA, MAD-3, NFKBI}, MUC5AC (mucin 5AC, oligomeric mucus/gel-forming) [NCBI Gene 4586] {aka MUC5, TBM, leB, mucin}, RELA (RELA proto-oncogene, NF-kB subunit) [NCBI Gene 5970] {aka AIF3BL3, CMCU, NFKB3, p65}, MAPK14 (mitogen-activated protein kinase 14) [NCBI Gene 1432] {aka CSBP, CSBP1, CSBP2, CSPB1, EXIP, Mxi2}, NFKB1 (nuclear factor kappa B subunit 1) [NCBI Gene 4790] {aka CVID12, EBP-1, KBF1, NF-kB, NF-kB1, NF-kappa-B1}, CXCL8 (C-X-C motif chemokine ligand 8) [NCBI Gene 3576] {aka GCP-1, GCP1, IL8, LECT, LUCT, LYNAP}, CCL2 (C-C motif chemokine ligand 2) [NCBI Gene 6347] {aka GDCF-2, HC11, HSMCR30, MCAF, MCP-1, MCP1}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, EIF2AK3 (eukaryotic translation initiation factor 2 alpha kinase 3) [NCBI Gene 9451] {aka PEK, PERK, WRS}, MAPK1 (mitogen-activated protein kinase 1) [NCBI Gene 5594] {aka ERK, ERK-2, ERK2, ERT1, MAPK2, NS13}, AQP5 (aquaporin 5) [NCBI Gene 362] {aka AQP-5, PPKB}
- **Diseases:** asthma (MESH:D001249), allergic conditions (MESH:D004342), Allergic rhinitis (MESH:D065631)
- **Chemicals:** Linarin (MESH:C008282), Histamine (MESH:D006632), SP600125 (MESH:C432165), SB203580 (MESH:C093642), U0126 (MESH:C113580), PDTC (MESH:C066229), flavonoid (MESH:D005419)
- **Species:** Homo sapiens (human, species) [taxon 9606]
- **Cell lines:** BEAS-2B — Homo sapiens (Human), Transformed cell line (CVCL_0168), hNECs — Sus scrofa (Pig), Transformed cell line (CVCL_A2GJ)

## Full text

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## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12955925/full.md

## References

40 references — full list in the complete paper: https://tomesphere.com/paper/PMC12955925/full.md

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Source: https://tomesphere.com/paper/PMC12955925