Cited by 35Skin Protection and Agingmelanin and skin pigmentationDermatologic Treatments and Research

High-dose squalene ingestion increases type I procollagen and decreases ultraviolet-induced DNA damage in human skin in vivo but is associated with transient adverse effects

Cho, S., Choi, C.-W., Lee, D. H., Won, C.-H., Kim, S. M., Lee, S., Lee, M.-J., Chung, J. H.·2009·Clinical and Experimental Dermatology

Abstract

BACKGROUND: Evidence for beneficial effects of squalene on ultraviolet (UV)-induced photoageing of the skin is lacking. AIM: To investigate whether squalene supplementation improves signs and molecular markers of photoageing in human skin in vivo. METHODS: In total, 40 female volunteers aged > 50 years received two different doses [13.5 g/day (low-dose group) and 27 g/day (high-dose group)] of squalene for 90 days. At baseline and at the completion of the study, facial wrinkles were measured using skin replicas. Skin samples were taken to compare type I procollagen and matrix metalloproteinase 1 mRNA levels by real-time reverse-transcriptase PCR, and for type I procollagen immunostaining. Skin samples were also taken 24 h after 2 x minimal erythema dose (MED) of UV irradiation before and after squalene intake to assess UV-induced thymine dimer formation and keratinocytic apoptosis. RESULTS: In total, 37 subjects completed the trial. Transient loose stool was experienced by 35% of volunteers in the low-dose group and 55% in the high-dose group. Facial wrinkles decreased significantly (P < 0.05) in the high-dose group, while procollagen type I mRNA levels and MED increased significantly in the low-dose group. Procollagen immunostaining tended to increase in both groups. Facial erythema decreased and pigmentation increased significantly in both groups. UV-induced keratinocytic apoptosis and thymine dimer staining were substantially reduced in both groups. CONCLUSIONS: Daily ingestion of 13.5 or 27 g of squalene per day resulted in antiageing effects in photoaged skin. However, in view of the frequent incidence of loose stool experienced by the subjects, the risk-benefit ratio of high-dose squalene supplementation is too high to recommend it for treating skin ageing.

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Crossref · 10.1111/j.1365-2230.2008.03133.x

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  • In a clinical study, oral supplementation with squalene substantially increased procollagen levels and reduced facial wrinkles and erythema, keratinocytic apoptosis, and thymine dimer levels in facial skin.

    “In a clinical study, oral supplementation with squalene substantially increased procollagen levels and reduced facial wrinkles and erythema, keratinocytic apoptosis, and thymine dimer levels in facial skin [131].”

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Authors
Cho, S., Choi, C.-W., Lee, D. H., Won, C.-H., Kim, S. M., Lee, S., Lee, M.-J., & Chung, J. H.
Affiliations
Seoul National University (KR)
Corresponding author
Chung, J. H.
Venue
Clinical and Experimental Dermatology
Published
2009-06
Volume
34
Issue
4
Pages
500-508
ISSN
  • 0307-6938 (ISSN-L)
  • 1365-2230
OpenAlex
W2009166805
Cited by
35
References
21
Citations by year
2026: 1 · 2025: 1 · 2024: 4 · 2023: 4 · 2022: 1 · 2021: 2 · 2020: 4 · 2019: 3 · 2018: 2 · 2017: 1 · 2016: 2 · 2015: 1 · 2014: 6 · 2013: 1
FWCI
0.83
Type
journal article
Language
en
Open access
closed
Locations
  • Clinical and Experimental Dermatology (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Health Sciences › Medicine › Dermatology › Skin Protection and Aging
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › melanin and skin pigmentation
  • Health Sciences › Medicine › Dermatology › Dermatologic Treatments and Research
Keywords
squalene, dietary supplementation, photoaging, skin aging, type I procollagen, MMP-1, ultraviolet radiation, thymine dimers, keratinocyte apoptosis, facial wrinkles, facial erythema, skin pigmentation, gastrointestinal adverse effects, risk-benefit ratio
MeSH terms
Aged, Diarrhea, DNA Damage, Female, Humans, Middle Aged, Skin Pigmentation, Squalene, Ultraviolet Rays, Skin Aging, Treatment Outcome, Dietary Supplements, Matrix Metalloproteinase 1, Collagen Type I, Steatorrhea

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