Evidence map›Paper›PMID 39965555›Full record

ArticleSkin pharmacology and physiology2025

Skin Transcriptomic Analysis Reveals Altered Fatty Acid Metabolism Pathways in Mice Subjected to Sleep Fragmentation.

Da-Been Lee, Seung-Lim Yoo, June Seok Heo, Ja-Yun Lim, Sang Shin Pyo, Ji Sun Moon, Mi-Ran Lee, Jinkwan Kim, Suhng-Wook Kim, Dae-Wui Yoon

Abstract read
In one paragraph

Article in Skin pharmacology and physiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Da-Been LeeHealth Science Research Center, College of Health Science, Korea University, Seoul, Republic of Korea.
Seung-Lim YooSleep Medicine Institute, Jungwon University, Goesan, Republic of Korea.
June Seok HeoCell Therapy Center, Severance Hospital, Seoul, Republic of Korea.
Ja-Yun LimCarbohydrate Bioproduct Research Center, Sejong University, Seoul, Republic of Korea.
Sang Shin PyoDepartment of Biomedical Laboratory Science, Shinhan University, Uijeongbu-si, Republic of Korea.
Ji Sun MoonDepartment of Medical Beauty Care, Jungwon University, Goesan, Republic of Korea.
Mi-Ran LeeDepartment of Biomedical Laboratory Science, Jungwon University, Goesan, Republic of Korea.
Jinkwan KimSleep Medicine Institute, Jungwon University, Goesan, Republic of Korea.
Suhng-Wook KimHealth Science Research Center, College of Health Science, Korea University, Seoul, Republic of Korea.
Dae-Wui YoonSleep Medicine Institute, Jungwon University, Goesan, Republic of Korea.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionSleep fragmentation (SF) is a hallmark of sleep disorders and has been associated with systemic health issues, but its specific impact on skin health remains unclear. This study aimed to investigate whether SF impairs skin barrier function and identify the biological pathways involved in SF-induced skin damage.

methodsTwenty-four 6-week-old male BALB/c mice were divided into home cage control (HC) and SF groups. SF was induced using a commercially available SF chamber. Skin barrier function was assessed by measuring transepidermal water loss (TEWL) at 4 and 8 weeks. Epidermal thickness and dermal collagen density were also measured. Total RNA sequencing (RNA-Seq) and bioinformatics analysis were conducted to identify the affected pathways.

resultsTEWL was significantly higher in the SF group than in the HC group at 8 weeks. Epidermal thickness and dermal collagen density were significantly lower in the SF group than in the HC group. In the SF group, 133 differentially expressed genes were identified, of which 14 were upregulated and 119 were downregulated. RNA-Seq and bioinformatics analysis revealed an altered fatty acid metabolism pathway in the skin of mice subjected to chronic SF. This was validated through quantitative real-time polymerase chain reaction.

conclusionSF caused physiological and histological changes in the skin, altering the fatty acid metabolism pathway. The role of this pathway in SF-induced skin damage requires further exploration.

Indexed as

Fatty AcidsSkinSleep DeprivationTranscriptomeAnimalsCollagenGene Expression ProfilingMaleMiceMice, Inbred BALB CWater Loss, InsensibleCollagenFatty AcidsFatty acid metabolismRNA sequencingSkin barrier functionSleep fragmentation

Identifiers

PMID39965555
PMCPMC12136610

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.