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Updated: Feb 6, 2026

Studying Chronic Exposure of Mice to Ultraviolet B Radiation
Published on: August 19, 2025
Anti-Photoaging Effects of Low Molecular-Weight Fucoidan on Ultraviolet B-Irradiated Mice
Young-In Kim1,2, Won-Seok Oh3, Phil Hyun Song4
1Department of Veterinary Internal Medicine, College of Veterinary Medicine, Kyungpook National University, Daegu 41566, Korea. kimyoungin@kpclab.co.kr.
Abstract:
Ultraviolet (UV) B exposure induces DNA damage and production of reactive oxygen species (ROS), which causes skin photoaging through signaling pathways of inflammation and modulation of extracellular matrix remodeling proteins, collagens, and matrix metalloproteinase (MMP). As low molecular-weight fucoidan (LMF) has potential antioxidant and anti-inflammatory properties, we examined the protective effects of LMF against UVB-induced photoaging. A UVB-irradiated mouse model was topically treated with myricetin or LMF at 2.0, 1.0 and 0.2 mg/cm² (LMF2.0, LMF1.0 and LMF0.2, respectively) once a day for 15 weeks. Wrinkle formation, inflammation, oxidative stress, MMP expression, and apoptosis in the treated regions were compared with those in a distilled water-treated photoaging model (UVB control). LMF treatments, particularly LMF2.0 and LMF1.0, significantly inhibited the wrinkle formation, skin edema, and neutrophil recruitment into the photo-damaged lesions, compared with those in the UVB control. While LMF decreased interleukin (IL)-1β release, it increased IL-10. The LMF treatment inhibited the oxidative stresses (malondialdehyde and superoxide anion) and enhanced endogenous antioxidants (glutathione). Additionally, LMF reduced the mRNA expression of MMP-1, 9, and 13. The histopathological analyses revealed the anti-photoaging effects of LMF exerted via its antioxidant, anti-apoptotic, and MMP-9-inhibiting effects. These suggest that LMF can be used as a skin-protective remedy for photoaging.
Insights
Low molecular-weight fucoidan (LMF) effectively protects skin from UV damage. LMF reduces wrinkles, inflammation, and oxidative stress, acting as a potent antioxidant and anti-inflammatory agent for photoaging prevention.
Area of Science:
- Dermatology
- Biochemistry
- Marine Biotechnology
Background:
- Ultraviolet (UV) B radiation causes skin photoaging via DNA damage, reactive oxygen species (ROS), inflammation, and extracellular matrix degradation.
- Low molecular-weight fucoidan (LMF) exhibits known antioxidant and anti-inflammatory properties.
- Understanding LMF's protective mechanisms against UVB-induced skin damage is crucial.
Purpose of the Study:
- To investigate the protective effects of LMF against UVB-induced photoaging in a mouse model.
- To evaluate LMF's impact on wrinkle formation, inflammation, oxidative stress, matrix metalloproteinase (MMP) expression, and apoptosis.
Main Methods:
- A UVB-irradiated mouse model was topically treated with varying concentrations of LMF (0.2, 1.0, and 2.0 mg/cm²) daily for 15 weeks.
- Evaluated parameters included wrinkle formation, skin edema, inflammatory markers (IL-1β, IL-10), oxidative stress markers (malondialdehyde, superoxide anion, glutathione), MMP mRNA expression (MMP-1, 9, 13), and apoptosis.
- Histopathological analyses were performed to assess anti-photoaging effects.
Main Results:
- LMF treatments, particularly at 1.0 and 2.0 mg/cm², significantly reduced wrinkle formation, skin edema, and neutrophil infiltration.
- LMF modulated inflammatory cytokines, decreasing IL-1β and increasing IL-10.
- LMF inhibited oxidative stress, reduced malondialdehyde and superoxide anion levels, and enhanced glutathione, while decreasing MMP-1, 9, and 13 mRNA expression.
Conclusions:
- LMF demonstrates significant anti-photoaging effects by mitigating UVB-induced skin damage.
- Its protective mechanisms involve potent antioxidant, anti-inflammatory, anti-apoptotic, and MMP-inhibiting activities.
- LMF shows promise as a topical agent for preventing and treating skin photoaging.
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