Evidence map›Paper›PMID 40295857›Full record

ArticleInternational journal of obesity (2005)2025

Ultraviolet exposure of mice fed a high fat diet reduces weight gain and markers of liver disease progression.

Gareth Hazell, Marina Khazova, Hannah Mancey, Raymond Shek, Paul O'Mahoney

Abstract read
In one paragraph

Article in International journal of obesity (2005), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

1 citing paper in PubMed.

  1. Article
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

5 authors.

Gareth HazellUK Health Security Agency, Chilton, Didcot, OX11 0RQ, UK. gareth.hazell@ukhsa.gov.uk.ORCID 0009-0004-2613-9833
Marina KhazovaUK Health Security Agency, Chilton, Didcot, OX11 0RQ, UK.
Hannah ManceyUK Health Security Agency, Chilton, Didcot, OX11 0RQ, UK.
Raymond ShekUK Health Security Agency, Chilton, Didcot, OX11 0RQ, UK.
Paul O'MahoneyUK Health Security Agency, Chilton, Didcot, OX11 0RQ, UK.ORCID 0000-0003-3221-5105

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundResearch suggests that ultraviolet (UV) exposure of mice placed on a high fat diet can reduce incidence of metabolic disease. However, current research had primarily focused on male mice with UV outside level of terrestrial sunlight.

objectivesHere we attempt to address this imbalance, with a pilot study presented wherein female mice C57Bl6 mice are included, with UV exposure at level comparable to low dose (non-burning) sunlight exposure.

methods2% UV-B and 98% UV-At a dose of 1.83 J/cm

resultsNon-significant trends are observed for weight amelioration in UV exposed mice across both sexes at study endpoint, whereas in the liver, a reduction of lipid droplet size due to UV exposure is observed. Assessment of vitamin D status at study endpoint shows that the high fat diet increases 25(OH)D level in both sexes, more so in female mice, with further non-significant rises due to UV exposure.

conclusionsThis study supports previous evidence that non-vitamin D mediated pathways may be responsible for the outcomes reported in this study. The UV exposures used in this study also resulted in minimal damage to ex vivo skin or in vitro cells, as assessed by cyclobutene-pyrimidine dimers (CPD's) (characteristic signature mutations induced by UV), and double stranded breaks, further demonstrating the potential benefit of such exposures. This study supports and builds on current evidence that non-vitamin D pathways mediated through UV exposure may be beneficial in slowing weight gain and liver disease progression.

Indexed as

Diet, High-FatLiver DiseasesUltraviolet RaysWeight GainAnimalsBiomarkersDisease ProgressionFemaleMaleMiceMice, Inbred C57BLPilot ProjectsBiomarkers

Identifiers

PMID40295857
PMCPMC12283362

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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.