# From Chronic Inflammation to Remodeling: Anthocyanins in the Context of Asthma Management

**Authors:** Madiha Ajaz, Indu Singh, Lada Vugic, Rati Jani, Ayesha Zahid, Natalie Shilton

PMC · DOI: 10.3390/ph19020323 · 2026-02-15

## TL;DR

This paper explores how anthocyanins, natural compounds with anti-inflammatory properties, may help manage asthma by potentially reducing inflammation and airway remodeling.

## Contribution

The paper highlights anthocyanins' potential to target the PAI-1 pathway in asthma, a novel angle for managing the disease.

## Key findings

- Anthocyanins reduce asthma-related inflammatory cytokines and chemokines in preclinical models.
- Higher anthocyanin intake is epidemiologically linked to lower asthma risk and better lung function.
- Anthocyanins may reduce PAI-1 levels in other chronic conditions, suggesting relevance to asthma.

## Abstract

Asthma is a prevalent chronic disease posing substantial health and economic challenges globally. Its progression involves key hallmarks such as inflammation and airway remodeling, mediated by multiple inflammatory biomarkers and pathways. Despite the availability of potent therapeutic options, many patients continue to suffer from uncontrolled asthma. The plasminogen activator inhibitor-1 (PAI-1) signaling pathway is critical in asthma exacerbation and remodeling, with elevated PAI-1 levels linked to disease progression. Anthocyanins (ACNs), potent antioxidants and anti-inflammatory compounds, have shown promise in asthma management. Epidemiological studies associate higher ACN intake with a lower risk of asthma and improved lung function. Preclinical models further demonstrate ACNs’ effectiveness in reducing asthma-related inflammatory cytokines, chemokines, and signaling pathways. Additionally, a human trial suggests ACNs can improve symptom control and lung function. While no direct evidence links ACNs to PAI-1 reduction in asthma, studies in other chronic conditions show ACNs reduce PAI-1 levels, supporting their potential role in asthma. This suggests a promising avenue for exploring their effects on airway remodeling. The lack of robust human studies remains a gap. Future research should focus on establishing direct evidence of ACNs’ impact on PAI-1 levels and remodeling in asthma, providing novel insights into managing asthma as an adjunct.

## Linked entities

- **Proteins:** SERPINE1 (serpin family E member 1)
- **Chemicals:** anthocyanins (PubChem CID 145858)
- **Diseases:** asthma (MONDO:0004979)

## Full-text entities

- **Genes:** CCL5 (C-C motif chemokine ligand 5) [NCBI Gene 6352] {aka D17S136E, RANTES, SCYA5, SIS-delta, SISd, TCP228}, Il6 (interleukin 6) [NCBI Gene 16193] {aka Il-6}, Il18 (interleukin 18) [NCBI Gene 16173] {aka Igif, Il-18}, SIRT1 (sirtuin 1) [NCBI Gene 23411] {aka SIR2, SIR2L1, SIR2alpha}, CCL11 (C-C motif chemokine ligand 11) [NCBI Gene 6356] {aka SCYA11}, CCL26 (C-C motif chemokine ligand 26) [NCBI Gene 10344] {aka IMAC, MIP-4a, MIP-4alpha, SCYA26, TSC-1}, IL33 (interleukin 33) [NCBI Gene 90865] {aka C9orf26, DVS27, IL1F11, NF-HEV, NFEHEV}, TP53 (tumor protein p53) [NCBI Gene 7157] {aka BCC7, BMFS5, LFS1, P53, TRP53}, Chil3 (chitinase-like 3) [NCBI Gene 12655] {aka Chi3l3, ECF-L, Ym1}, SMAD4 (SMAD family member 4) [NCBI Gene 4089] {aka DPC4, JIP, MADH4, MYHRS}, PLAU (plasminogen activator, urokinase) [NCBI Gene 5328] {aka ATF, BDPLT5, QPD, UPA, URK, u-PA}, Vcam1 (vascular cell adhesion molecule 1) [NCBI Gene 22329] {aka CD106, Vcam-1}, Retnla (resistin like alpha) [NCBI Gene 57262] {aka 1810019L16Rik, Fizz-1, Fizz1, HIMF, RELM-alpha, RELMa}, FOXP3 (forkhead box P3) [NCBI Gene 50943] {aka AIID, DIETER, IPEX, JM2, PIDX, XPID}, 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}, ACTA1 (actin alpha 1, skeletal muscle) [NCBI Gene 58] {aka ACTA, ASMA, CFTD, CFTD1, CFTDM, CMYO2A}, TRIM63 (tripartite motif containing 63) [NCBI Gene 84676] {aka CMH31, IRF, MURF1, MURF2, RNF28, SMRZ}, Il13 (interleukin 13) [NCBI Gene 16163] {aka Il-13}, STAT6 (signal transducer and activator of transcription 6) [NCBI Gene 6778] {aka D12S1644, HIES6, IL-4-STAT, STAT6B, STAT6C}, Plau (plasminogen activator, urokinase) [NCBI Gene 18792] {aka u-PA, uPA}, Icam1 (intercellular adhesion molecule 1) [NCBI Gene 15894] {aka CD54, Icam-1, Ly-47, MALA-2}, Vegfa (vascular endothelial growth factor A) [NCBI Gene 22339] {aka L-VEGF, Vegf, Vpf}, Crp (C-reactive protein, pentraxin-related) [NCBI Gene 12944], CRYGC (crystallin gamma C) [NCBI Gene 1420] {aka CCL, CRYG3, CTRCT2}, Il1b (interleukin 1 beta) [NCBI Gene 16176] {aka IL-1beta, Il-1b}, Il5 (interleukin 5) [NCBI Gene 16191] {aka Il-5}, Gata3 (GATA binding protein 3) [NCBI Gene 14462] {aka Gata-3, jal}, PLG (plasminogen) [NCBI Gene 5340] {aka HAE4}, RORC (RAR related orphan receptor C) [NCBI Gene 6097] {aka IMD42, NR1F3, RORG, RZR-GAMMA, RZRG, TOR}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, Ccl2 (C-C motif chemokine ligand 2) [NCBI Gene 20296] {aka HC11, JE, MCAF, MCP-1, MCP1, SMC-CF}, IGHE (immunoglobulin heavy constant epsilon) [NCBI Gene 3497] {aka IgE}, GATA3 (GATA binding protein 3) [NCBI Gene 2625] {aka HDR, HDRS}, PTGDR2 (prostaglandin D2 receptor 2) [NCBI Gene 11251] {aka CD294, CRTH2, DL1R, DP2, GPR44}, Stat6 (signal transducer and activator of transcription 6) [NCBI Gene 20852], Cxcl10 (C-X-C motif chemokine ligand 10) [NCBI Gene 15945] {aka C7, CRG-2, INP10, IP-10, IP10, Ifi10}, Cat (catalase) [NCBI Gene 12359] {aka 2210418N07, Cas-1, Cas1, Cs-1}, Ccl4 (C-C motif chemokine ligand 4) [NCBI Gene 20303] {aka AT744.1, Act-2, MIP-1B, Mip1b, Scya4}, TSLP (thymic stromal lymphopoietin) [NCBI Gene 85480], IL4 (interleukin 4) [NCBI Gene 3565] {aka BCGF-1, BCGF1, BSF-1, BSF1, IL-4}, SERPINE1 (serpin family E member 1) [NCBI Gene 5054] {aka PAI, PAI-1, PAI1, PLANH1}, Jak1 (Janus kinase 1) [NCBI Gene 16451] {aka BAP004, C130039L05Rik}, IFNG (interferon gamma) [NCBI Gene 3458] {aka IFG, IFI, IMD69}, PLAT (plasminogen activator, tissue type) [NCBI Gene 5327] {aka T-PA, TPA}, JUNB (JunB proto-oncogene, AP-1 transcription factor subunit) [NCBI Gene 3726] {aka AP-1}, PIK3CB (phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta) [NCBI Gene 5291] {aka P110BETA, PI3K, PI3KBETA, PIK3C1}, IL13 (interleukin 13) [NCBI Gene 3596] {aka IL-13, P600}, IL5 (interleukin 5) [NCBI Gene 3567] {aka EDF, IL-5, TRF}, Il10 (interleukin 10) [NCBI Gene 16153] {aka CSIF, If2a, Il-10}, TBX21 (T-box transcription factor 21) [NCBI Gene 30009] {aka IMD88, T-PET, T-bet, TBET, TBLYM}, NFE2L2 (NFE2 like bZIP transcription factor 2) [NCBI Gene 4780] {aka IMDDHH, NRF2, Nrf-2}, ELN (elastin) [NCBI Gene 2006] {aka ADCL1, SVAS, WBS, WS}, Il4 (interleukin 4) [NCBI Gene 16189] {aka BSF-1, Il-4}, TGFB1 (transforming growth factor beta 1) [NCBI Gene 7040] {aka CAEND1, CED, DPD1, IBDIMDE, LAP, TGF-beta1}, CAT (catalase) [NCBI Gene 847], CX3CL1 (C-X3-C motif chemokine ligand 1) [NCBI Gene 6376] {aka ABCD-3, C3Xkine, CXC3, CXC3C, NTN, NTT}, CASP1 (caspase 1) [NCBI Gene 834] {aka ICE, IL1BC, P45}, Arg1 (arginase, liver) [NCBI Gene 11846] {aka AI, Arg-1, PGIF}, Serpinb2 (serine (or cysteine) peptidase inhibitor, clade B, member 2) [NCBI Gene 18788] {aka PAI-2, Planh2, ovalbumin}
- **Diseases:** airway obstruction (MESH:D000402), renal ischemia (MESH:D007511), overweight (MESH:D050177), obesity (MESH:D009765), impaired pulmonary function (OMIM:608852), Asthma (MESH:D001249), swelling (MESH:D004487), cancer (MESH:D009369), diabetes (MESH:D003920), breathing difficulties (MESH:D004417), asthmatic (MESH:D013224), pain (MESH:D010146), fibrosis (MESH:D005355), ) inflammation (MESH:D007249), injury to (MESH:D014947), chronic (MESH:D002908), immune dysregulation (OMIM:614878), -2 (MESH:D020803), pulmonary fibrosis (MESH:D011658), wheezing (MESH:D012135), type 2 diabetes (MESH:D003924), hypercholesterolemic (MESH:D006938), cough (MESH:D003371), colitis (MESH:D003092), infections (MESH:D007239), inflammatory compounds (MESH:D005597)
- **Chemicals:** coumarin (MESH:C030123), phenolic acids (MESH:C017616), flavonols (MESH:D044948), carbon (MESH:D002244), 2,2-Diphenyl-1-picrylhydrazyl (MESH:C004931), salicylic acid (MESH:D020156), oxygen (MESH:D010100), flavone (MESH:C043562), sugar (MESH:D000073893), histamine (MESH:D006632), pelargonidin (MESH:C066957), metal (MESH:D008670), flavan-3-ol (MESH:C404987), saponins (MESH:D012503), reactive oxygen species (MESH:D017382), Calcium (MESH:D002118), flavonoid (MESH:D005419), cyanidin-3-O-glucoside (MESH:C462279), glucose (MESH:D005947), ACN (MESH:D000872), flavones (MESH:D047309), petunidin (MESH:C473206), ABTS+ (MESH:C002502), lipid (MESH:D008055), GSH (MESH:D005978), methyl ether (MESH:D008738), polyphenol (MESH:D059808), MDA (MESH:D008315), peonidin (MESH:C473205), Cyanidin (MESH:C017154), flavanones (MESH:D044950), proanthocyanidins (MESH:D044945), quercetin-3-O-glucoside (MESH:C016527), Delphinidin (MESH:C017185), malvidin (MESH:C065861), GAGs (MESH:D006025), Superoxide anion (MESH:D013481), ICS (-)
- **Species:** Berberis aquifolium (hollyleaf barberry, species) [taxon 203270], Cordyline fruticosa (good luck plant, species) [taxon 39501], Mus musculus (house mouse, species) [taxon 10090], Viola odorata (species) [taxon 97441], Oryza sativa (Asian cultivated rice, species) [taxon 4530], Solanum tuberosum (potatoes, species) [taxon 4113], Homo sapiens (human, species) [taxon 9606]
- **Mutations:** P13K
- **Cell lines:** A549 — Homo sapiens (Human), Lung adenocarcinoma, Cancer cell line (CVCL_0023), mast cell line-1 — Mus musculus (Mouse), Spontaneously immortalized cell line (CVCL_Y654), basal epithelial cell — Homo sapiens (Human), Telomerase immortalized cell line (CVCL_T028), HMC-1 — Homo sapiens (Human), Mast cell leukemia, Cancer cell line (CVCL_0003)

## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12943696/full.md

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Source: https://tomesphere.com/paper/PMC12943696