Is lack of sleep capable of inducing DNA damage in aged skin?
V Kahan1, D A Ribeiro, F Egydio
1Departamentos de Psicobiologia, Universidade Federal de São Paulo, São Paulo, Brazil.
Abstract:
Skin naturally changes with age, becoming more fragile. Various stimuli can alter skin integrity. The aim of this study was to evaluate whether sleep deprivation affects the integrity of DNA in skin and exacerbates the effects of aging. Fifteen-month old female Hairless mice underwent 72 h of paradoxical sleep deprivation or 15 days of chronic sleep restriction. Punch biopsies of the skin were taken to evaluate DNA damage by single cell gel (comet) assay. Neither paradoxical sleep deprivation nor sleep restriction increased genetic damage, measured by tail movement and tail intensity values. Taken together, the findings are consistent with the notion that aging overrides the effect of sleep loss on the genetic damage in elderly mice.
Insights
Aging skin
Area of Science:
- Gerontology and Dermatology
Background:
- Skin integrity naturally declines with age, making it more susceptible to damage.
- Various external factors can compromise skin health and structure.
Purpose of the Study:
- To investigate the impact of sleep deprivation on skin DNA integrity.
- To determine if sleep loss worsens age-related skin damage.
Main Methods:
- Female Hairless mice (15 months old) were subjected to either 72 hours of paradoxical sleep deprivation or 15 days of chronic sleep restriction.
- Skin biopsies were analyzed for DNA damage using the single cell gel (comet) assay.
Main Results:
- Neither acute paradoxical sleep deprivation nor chronic sleep restriction resulted in increased DNA damage in the mice's skin.
- Measurements of tail movement and tail intensity in the comet assay showed no significant changes due to sleep manipulation.
Conclusions:
- In aged mice, the natural aging process appears to be a more dominant factor influencing skin DNA integrity than sleep deprivation.
- Sleep loss did not exacerbate genetic damage in the skin of elderly mice under the study conditions.
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