# Quercus acuta Acorn Bran Extract Enhances Wound Healing by Promoting Human Dermal Fibroblast Migration and Antioxidant Activity

**Authors:** So-An Lim, Tae Hyun Son, Hye-Lim Shin, Dongsoo Kim, Jun-Hyuck Yoon, Hwan-Gyu Kim, Hyunmo Choi, Shin-Hye Kim, Sik-Won Choi

PMC · DOI: 10.3390/ph19030481 · Pharmaceuticals · 2026-03-15

## TL;DR

A natural extract from Quercus acuta acorn bran improves wound healing by boosting cell activity and reducing oxidative stress.

## Contribution

The study demonstrates QAABE's novel ability to enhance fibroblast migration and antioxidant activity for wound healing.

## Key findings

- QAABE upregulates extracellular matrix markers like vimentin and VEGF in human dermal fibroblasts.
- QAABE shows ROS-scavenging activity and accelerates wound closure in a mouse model.
- QAABE reduces inflammatory responses during skin injury recovery.

## Abstract

Background/Objectives: Wound repair-associated processes and the antioxidant properties of natural products play critical roles in skin wound healing and barrier restoration. Wound healing is a complex process characterized by a series of interconnected events that facilitate the self-repair of the skin following injury. Methods: This study aimed to evaluate the effects of Quercus acuta acorn bran extract (QAABE) on wound healing using human dermal fibroblast (HDF) cell cultures treated with QAABE. Additionally, in vivo experiments were conducted using a mouse model of skin injury to assess the wound-healing potential of the extract. Results: The results indicated that QAABE enhanced wound healing in vitro by upregulating extracellular matrix-related markers, including vimentin, Col1a1, Col3a1, endothelin, fibronectin, and VEGF at the mRNA level, and increasing the protein expression of vimentin, COL1A1, endothelin, and α-SMA. QAABE also exhibited reactive oxygen species (ROS)-scavenging activity. In the mouse skin injury model, QAABE treatment accelerated wound closure and was associated with reduced inflammatory responses. Conclusions: These findings suggest that QAABE may promote wound-healing-related responses in both in vitro and in vivo models, supporting its potential as a candidate for further investigation in wound-healing research.

## Linked entities

- **Genes:** PRELID1 (PRELI domain containing 1) [NCBI Gene 737446], COL1A1 (collagen type I alpha 1 chain) [NCBI Gene 1277], COL3A1 (collagen type III alpha 1 chain) [NCBI Gene 1281], fn1.S (fibronectin 1 S homeolog) [NCBI Gene 397744], VEGFA (vascular endothelial growth factor A) [NCBI Gene 7422], COL1A1 (collagen type I alpha 1 chain) [NCBI Gene 1277], ACTA1 (actin alpha 1, skeletal muscle) [NCBI Gene 58]
- **Species:** Quercus acuta (taxon 157796), Mus musculus (taxon 10090)

## Full-text entities

- **Genes:** FN1 (fibronectin 1) [NCBI Gene 2335] {aka CIG, ED-B, FINC, FN, FNZ, GFND}, VIM (vimentin) [NCBI Gene 7431], ACTA1 (actin alpha 1, skeletal muscle) [NCBI Gene 58] {aka ACTA, ASMA, CFTD, CFTD1, CFTDM, CMYO2A}, COL3A1 (collagen type III alpha 1 chain) [NCBI Gene 1281] {aka EDS4A, EDSVASC, PMGEDSV}, COL1A1 (collagen type I alpha 1 chain) [NCBI Gene 1277] {aka CAFYD, EDSARTH1, EDSC, OI1, OI2, OI3}, VEGFA (vascular endothelial growth factor A) [NCBI Gene 7422] {aka L-VEGF, MVCD1, VEGF, VPF}
- **Diseases:** skin injury (MESH:D000069836), inflammatory (MESH:D007249)
- **Chemicals:** QAABE (-), ROS (MESH:D017382)
- **Species:** Mus musculus (house mouse, species) [taxon 10090], Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13029716/full.md

## References

35 references — full list in the complete paper: https://tomesphere.com/paper/PMC13029716/full.md

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Source: https://tomesphere.com/paper/PMC13029716