# From Sea to Sight: Fucoidan Protects Against Oxidative Damage in Porcine Retina Organ Culture

**Authors:** Leonie Deppe, Philipp Dörschmann, H. Burkhard Dick, Alexa Klettner, Stephanie C. Joachim

PMC · DOI: 10.3390/md24030088 · Marine Drugs · 2026-02-24

## TL;DR

This study shows that fucoidan, a compound from algae, protects retinal cells from oxidative damage in a lab model, suggesting it could be a potential treatment for glaucoma.

## Contribution

The study demonstrates fucoidan's protective effects against oxidative stress in retinal ganglion cells using a porcine retina organ culture model.

## Key findings

- Fucoidan prevented retinal ganglion cell loss and reduced oxidative stress markers in the model.
- Fucoidan mitigated glial activation and microglia/macrophage infiltration caused by hydrogen peroxide.
- Fucoidan restored anti-oxidative gene expression and reduced apoptotic and ferroptotic signaling.

## Abstract

Degeneration of retinal ganglion cells (RGCs) is a hallmark of glaucoma. As RGCs are vulnerable to oxidative imbalance, anti-oxidative strategies are of significant interest as novel therapeutic targets. Fucoidans, bioactive compounds derived from algae, are known to be anti-oxidative. Hence, we investigated if fucoidans have protective effects in a retina organ culture model. Porcine explants were pre-treated with fucoidan (Fucus vesiculosus; FVs) for 0.5 h (10 or 50 µg/mL). Afterwards, damage was induced through H2O2 (500 µM; 3 h). Four groups were investigated: control, H2O2, 10 FVs + H2O2, and 50 FVs + H2O2. RGCs, glial cells, hypoxic/oxidative, apoptotic, and ferroptotic markers were examined by immunohistology, RT-qPCR, and a caspase assay. H2O2 led to lower RGC numbers and RBPMS expression levels while FVs prevented this degeneration. An upregulation of glial expressions and more microglia/macrophages were observed in H2O2 samples, mitigated by FVs. Anti-oxidative genes increased during stress but normalized with FVs. Apoptotic signaling increased while GPX4 mRNA expression decreased with H2O2, both restored by FVs. Consequently, RGC loss was prevented through the attenuation of glial activation, inhibition of hypoxic/oxidative stress, and anti-ferroptotic/apoptotic action mediated by FVs. Advancing glaucoma research, this study emphasizes the therapeutic potential of FVs and offers new directions for future research.

## Linked entities

- **Genes:** RBPMS (RNA binding protein, mRNA processing factor) [NCBI Gene 11030], GPX4 (glutathione peroxidase 4) [NCBI Gene 2879]
- **Chemicals:** H2O2 (PubChem CID 784)
- **Diseases:** glaucoma (MONDO:0005041)
- **Species:** Sus scrofa (taxon 9823)

## Full-text entities

- **Genes:** JUNB (JunB proto-oncogene, AP-1 transcription factor subunit) [NCBI Gene 3726] {aka AP-1}, MAPK1 (mitogen-activated protein kinase 1) [NCBI Gene 5594] {aka ERK, ERK-2, ERK2, ERT1, MAPK2, NS13}, Gpx4 (glutathione peroxidase 4) [NCBI Gene 625249] {aka GPx-4, GSHPx-4, PHGPx, mtPHGPx, snGPx}, HIF1A (hypoxia inducible factor 1 subunit alpha) [NCBI Gene 3091] {aka HIF-1-alpha, HIF-1A, HIF-1alpha, HIF1, HIF1-ALPHA, MOP1}, MAPK14 (mitogen-activated protein kinase 14) [NCBI Gene 1432] {aka CSBP, CSBP1, CSBP2, CSPB1, EXIP, Mxi2}, Nfe2l2 (nuclear factor, erythroid derived 2, like 2) [NCBI Gene 18024] {aka Nrf2}, Hmox1 (heme oxygenase 1) [NCBI Gene 15368] {aka D8Wsu38e, HO-1, HO1, Hemox, Hmox, Hsp32}, H3-3A (H3.3 histone A) [NCBI Gene 3020] {aka BRYLIB1, H3.3A, H3F3, H3F3A}, NFKB1 (nuclear factor kappa B subunit 1) [NCBI Gene 4790] {aka CVID12, EBP-1, KBF1, NF-kB, NF-kB1, NF-kappa-B1}, AKT1 (AKT serine/threonine kinase 1) [NCBI Gene 207] {aka AKT, PKB, PKB-ALPHA, PRKBA, RAC, RAC-ALPHA}, Tnf (tumor necrosis factor) [NCBI Gene 21926] {aka DIF, TNF-a, TNF-alpha, TNFSF2, TNFalpha, Tnfa}, Sod2 (superoxide dismutase 2, mitochondrial) [NCBI Gene 20656] {aka MnSOD, Sod-2}, NOS2 (nitric oxide synthase 2) [NCBI Gene 4843] {aka HEP-NOS, INOS, NOS, NOS2A}, Ifng (interferon gamma) [NCBI Gene 15978] {aka IFN-g, If2f, Ifg}, Cat (catalase) [NCBI Gene 12359] {aka 2210418N07, Cas-1, Cas1, Cs-1}, PIK3CB (phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta) [NCBI Gene 5291] {aka P110BETA, PI3K, PI3KBETA, PIK3C1}, MTOR (mechanistic target of rapamycin kinase) [NCBI Gene 2475] {aka FRAP, FRAP1, FRAP2, RAFT1, RAPT1, SKS}, GAPDH (glyceraldehyde-3-phosphate dehydrogenase) [NCBI Gene 2597] {aka G3PD, GAPD, HEL-S-162eP}, Il6 (interleukin 6) [NCBI Gene 16193] {aka Il-6}
- **Diseases:** neuroinflammatory injury (MESH:D000090862), Parkinson's disease (MESH:D010300), deficiency of ATP (OMIM:614052), neurodegeneration (MESH:D019636), inflammatory cytokines (MESH:D000080424), ischemia (MESH:D007511), injury to (MESH:D014947), Glaucoma (MESH:D005901), Degeneration of retinal ganglion cells (MESH:D012162), corneal thinning (MESH:D013851), hypothermia (MESH:D007035), cardiotoxicity (MESH:D066126), Hypoxic (MESH:D002534), inflammation (MESH:D007249), Myopia (MESH:D009216), degeneration of the optic nerve (MESH:D009410), AMD (MESH:D008268), blindness (MESH:D001766), gliosis (MESH:D005911), RGC loss (MESH:D016388), Hypoxia (MESH:D000860)
- **Chemicals:** DAPI (MESH:C007293), alcohol (MESH:D000438), iron (MESH:D007501), doxorubicin (MESH:D004317), polysaccharide (MESH:D011134), rotenone (MESH:D012402), galactose (MESH:D005690), K (MESH:D011188), coenzyme Q10 (MESH:C024989), sulfate (MESH:D013431), polymers (MESH:D011108), xylose (MESH:D014994), 4',6'-Diamidin-2-phenylindol (-), streptomycin (MESH:D013307), SYBR Green I (MESH:C098022), L-fucose (MESH:D005643), L-glutamine (MESH:D005973), TritonX (MESH:D017830), O (MESH:D010100), CO2 (MESH:D002245), LPS (MESH:D008070), uronic acids (MESH:D014574), CoCl2 (MESH:C018021), glucose (MESH:D005947), N2 (MESH:D009584), mannose (MESH:D008358), sugars (MESH:D000073893), water (MESH:D014867), polyunsaturated fatty acids (MESH:D005231), ROS (MESH:D017382), lipid hydroperoxides (MESH:D008054), Fucoidan (MESH:C007789), glutathione (MESH:D005978), phospholipids (MESH:D010743), PBS (MESH:D007854), penicillin (MESH:D010406), H2O2 (MESH:D006861), FVs (MESH:C536525)
- **Species:** Fucus distichus (species) [taxon 3012], Homo sapiens (human, species) [taxon 9606], Fucus vesiculosus (species) [taxon 49266], Saccharina japonica (species) [taxon 88149], Mus musculus (house mouse, species) [taxon 10090], Severe acute respiratory syndrome coronavirus 2 (no rank) [taxon 2697049], Ascophyllum nodosum (species) [taxon 52969], Phaeophyceae (brown algae, class) [taxon 2870], Sus scrofa (pig, species) [taxon 9823], PX clade (clade) [taxon 569578], Rattus norvegicus (brown rat, species) [taxon 10116]
- **Cell lines:** ARPE-19 — Homo sapiens (Human), Spontaneously immortalized cell line (CVCL_0145), GCL-INL — Mus musculus (Mouse), Transformed cell line (CVCL_A1LI)

## Full text

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## Figures

8 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13028070/full.md

## References

103 references — full list in the complete paper: https://tomesphere.com/paper/PMC13028070/full.md

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Source: https://tomesphere.com/paper/PMC13028070