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Updated: May 17, 2025

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Assessment of Acute Wound Healing using the Dorsal Subcutaneous Polyvinyl Alcohol Sponge Implantation and Excisional Tail Skin Wound Models.
Published on: March 25, 2020
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Maresin-1 impairs cutaneous wound healing response
Reiko Hara1, Natsuko Saito-Sasaki1, Yu Sawada1
1Department of Dermatology, University of Occupational and Environmental Health, Kitakyushu, Fukuoka, Japan.
Immunohorizons
|April 2, 2025
Summary
Maresin-1, an anti-inflammatory compound, delays cutaneous wound healing by suppressing re-epithelization and keratinocyte migration. This occurs due to reduced tumor necrosis factor alpha in maresin-1 treated skin.
Area of Science:
- Biomedical Science
- Dermatology
- Inflammation Research
Background:
- Maresin-1 is a docosahexaenoic acid derivative known for potent anti-inflammatory effects.
- Inflammation is crucial for effective cutaneous wound healing.
- The role of maresin-1 in wound healing requires further investigation.
Purpose of the Study:
- To investigate the impact of maresin-1 on cutaneous wound healing.
- To elucidate the mechanisms by which maresin-1 affects wound repair.
Main Methods:
- Treatment of mouse skin wounds with maresin-1.
- Histological analysis of wound healing progression.
- Quantitative polymerase chain reaction (qPCR) to assess gene expression.
- Assessment of keratinocyte migration in vitro.
Main Results:
- Maresin-1 significantly delayed wound healing in the early phase (days 1-3).
- Histology showed suppressed re-epithelization in maresin-1 treated wounds.
- Maresin-1 decreased tumor necrosis factor alpha (TNF-α) expression in wounded skin.
- Reduced TNF-α indirectly inhibited keratinocyte migration, contributing to delayed healing.
Conclusions:
- Maresin-1 exerts an inhibitory effect on cutaneous wound healing.
- The delay in healing is mediated by maresin-1's suppression of TNF-α and subsequent keratinocyte migration.
- These findings highlight a potential negative impact of maresin-1 in contexts requiring robust wound repair.

