# Evaluating the effect of fucoidan-alginate combined dressing on wound healing in rats with full-thickness skin removed

**Authors:** Guifa Wang, Nan Zhang, Xiaochen Zhang, Zihan Guo, Man Liu, Meilan Xue, Hui Liang

PMC · DOI: 10.22038/ijbms.2025.86338.18650 · Iranian Journal of Basic Medical Sciences · 2025-01-01

## TL;DR

This study shows that fucoidan-alginate dressings improve wound healing in rats by reducing inflammation and boosting collagen production.

## Contribution

The study introduces a novel fucoidan-alginate dressing that enhances wound healing through the TGF-β1/Smad pathway in a rat model.

## Key findings

- 5% fucoidan-alginate dressings significantly reduced inflammation markers TNF-α and IL-1β.
- The 5% fucoidan group showed increased TGF-β1 levels and collagen synthesis.
- Dressings activated the TGF-β1/Smad signaling pathway to promote wound healing.

## Abstract

This study aims to investigate the effects of fucoidan-alginate combined dressings on wound healing in rats with full-thickness skin defects and to explore the underlying mechanisms.

Male SD rats were divided into three groups (n=15): Control, 2% fucoidan, and 5% fucoidan. Full-thickness skin wounds were created on each rat. Fucoidan-alginate dressings were prepared by applying 20 mg/ml and 50 mg/ml fucoidan solutions to alginate dressings (2×2 cm), resulting in 2% and 5% (w/v) fucoidan-alginate combined dressings, respectively. The control group utilized alginate dressings. Wound healing was assessed through various methods, including wound area measurement, histopathological analysis, white blood cell counts, ELISA for TNF-α and IL-1β, Masson’s trichrome staining for collagen, immunohistochemistry for TGF-β1, and western blotting for TGF-β1 and Smad-related proteins.

The results revealed that wound healing was significantly more effective in rats treated with 5% fucoidan-alginate combined dressings. Compared to the control group (P<0.01) and the 2% FUC group (P<0.05), the 5% FUC group exhibited reduced inflammatory cell infiltration and lower levels of TNF-α and IL-1β. Moreover, in comparison to the control group, the 5% FUC group demonstrated a significant up-regulation in the mean density of TGF-β1 (P<0.01) and significantly elevated protein expression levels of Col I, α-SMA, and p-Smad2/3 (P<0.01). Additionally, a notable amount of collagen production was observed.

The findings suggested that fucoidan-alginate dressings promote wound healing, reduce inflammation, and enhance collagen synthesis in rats, likely via the TGF-β1/Smad signaling pathway.

## Linked entities

- **Proteins:** TGFB1 (transforming growth factor beta 1), ACTA1 (actin alpha 1, skeletal muscle)
- **Chemicals:** alginate (PubChem CID 5102882)
- **Species:** Rattus norvegicus (taxon 10116)

## Full-text entities

- **Genes:** Tgfb1 (transforming growth factor, beta 1) [NCBI Gene 59086] {aka Tgfb}, Tnf (tumor necrosis factor) [NCBI Gene 24835] {aka RATTNF, TNF-alpha, Tnfa}, Il1b (interleukin 1 beta) [NCBI Gene 24494] {aka IL-1F2}
- **Diseases:** skin defects (MESH:D012868), inflammation (MESH:D007249)
- **Chemicals:** FUC (-), Fucoidan (MESH:C007789), alginate (MESH:D000464)
- **Species:** Rattus norvegicus (brown rat, species) [taxon 10116]

## Full text

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## Figures

10 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12571181/full.md

## References

51 references — full list in the complete paper: https://tomesphere.com/paper/PMC12571181/full.md

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Source: https://tomesphere.com/paper/PMC12571181