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The impact of sleep deprivation and nighttime light exposure on clock gene expression in humans
AIM: To examine the effect of acute sleep deprivation under light conditions on the expression of two key clock genes, hPer2 and hBmal1, in peripheral blood mononuclear cells (PBMC) and on plasma melatonin and cortisol levels. METHODS: Blood samples were drawn from 6 healthy individuals at 4-hour in...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Croatian Medical Schools
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3195968/ https://www.ncbi.nlm.nih.gov/pubmed/21990077 http://dx.doi.org/10.3325/cmj.2011.52.594 |
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author | Kavčič, Pavel Rojc, Bojan Dolenc-Grošelj, Leja Claustrat, Bruno Fujs, Kristina Poljak, Mario |
author_facet | Kavčič, Pavel Rojc, Bojan Dolenc-Grošelj, Leja Claustrat, Bruno Fujs, Kristina Poljak, Mario |
author_sort | Kavčič, Pavel |
collection | PubMed |
description | AIM: To examine the effect of acute sleep deprivation under light conditions on the expression of two key clock genes, hPer2 and hBmal1, in peripheral blood mononuclear cells (PBMC) and on plasma melatonin and cortisol levels. METHODS: Blood samples were drawn from 6 healthy individuals at 4-hour intervals for three consecutive nights, including a night of total sleep deprivation (second night). The study was conducted in April-June 2006 at the University Medical Centre Ljubljana. RESULTS: We found a significant diurnal variation in hPer2 and hBmal1 expression levels under baseline (P < 0.001, F = 19.7, df = 30 for hPer2 and P < 0.001, F = 17.6, df = 30 for hBmal1) and sleep-deprived conditions (P < 0.001, F = 9.2, df = 30 for hPer2 and P < 0.001, F = 13.2, df = 30 for hBmal1). Statistical analysis with the single cosinor method revealed circadian variation of hPer2 under baseline and of hBmal1 under baseline and sleep-deprived conditions. The peak expression of hPer2 was at 13:55 ± 1:15 hours under baseline conditions and of hBmal1 at 16:08 ± 1:18 hours under baseline and at 17:13 ± 1:35 hours under sleep-deprived conditions. Individual cosinor analysis of hPer2 revealed a loss of circadian rhythm in 3 participants and a phase shift in 2 participants under sleep-deprived conditions. The plasma melatonin and cortisol rhythms confirmed a conventional alignment of the central circadian pacemaker to the habitual sleep/wake schedule. CONCLUSION: Our results suggest that 40-hour acute sleep deprivation under light conditions may affect the expression of hPer2 in PBMCs. |
format | Online Article Text |
id | pubmed-3195968 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Croatian Medical Schools |
record_format | MEDLINE/PubMed |
spelling | pubmed-31959682011-10-19 The impact of sleep deprivation and nighttime light exposure on clock gene expression in humans Kavčič, Pavel Rojc, Bojan Dolenc-Grošelj, Leja Claustrat, Bruno Fujs, Kristina Poljak, Mario Croat Med J Clinical Science AIM: To examine the effect of acute sleep deprivation under light conditions on the expression of two key clock genes, hPer2 and hBmal1, in peripheral blood mononuclear cells (PBMC) and on plasma melatonin and cortisol levels. METHODS: Blood samples were drawn from 6 healthy individuals at 4-hour intervals for three consecutive nights, including a night of total sleep deprivation (second night). The study was conducted in April-June 2006 at the University Medical Centre Ljubljana. RESULTS: We found a significant diurnal variation in hPer2 and hBmal1 expression levels under baseline (P < 0.001, F = 19.7, df = 30 for hPer2 and P < 0.001, F = 17.6, df = 30 for hBmal1) and sleep-deprived conditions (P < 0.001, F = 9.2, df = 30 for hPer2 and P < 0.001, F = 13.2, df = 30 for hBmal1). Statistical analysis with the single cosinor method revealed circadian variation of hPer2 under baseline and of hBmal1 under baseline and sleep-deprived conditions. The peak expression of hPer2 was at 13:55 ± 1:15 hours under baseline conditions and of hBmal1 at 16:08 ± 1:18 hours under baseline and at 17:13 ± 1:35 hours under sleep-deprived conditions. Individual cosinor analysis of hPer2 revealed a loss of circadian rhythm in 3 participants and a phase shift in 2 participants under sleep-deprived conditions. The plasma melatonin and cortisol rhythms confirmed a conventional alignment of the central circadian pacemaker to the habitual sleep/wake schedule. CONCLUSION: Our results suggest that 40-hour acute sleep deprivation under light conditions may affect the expression of hPer2 in PBMCs. Croatian Medical Schools 2011-10 /pmc/articles/PMC3195968/ /pubmed/21990077 http://dx.doi.org/10.3325/cmj.2011.52.594 Text en Copyright © 2011 by the Croatian Medical Journal. All rights reserved. http://creativecommons.org/licenses/by/2.5/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Clinical Science Kavčič, Pavel Rojc, Bojan Dolenc-Grošelj, Leja Claustrat, Bruno Fujs, Kristina Poljak, Mario The impact of sleep deprivation and nighttime light exposure on clock gene expression in humans |
title | The impact of sleep deprivation and nighttime light exposure on clock gene expression in humans |
title_full | The impact of sleep deprivation and nighttime light exposure on clock gene expression in humans |
title_fullStr | The impact of sleep deprivation and nighttime light exposure on clock gene expression in humans |
title_full_unstemmed | The impact of sleep deprivation and nighttime light exposure on clock gene expression in humans |
title_short | The impact of sleep deprivation and nighttime light exposure on clock gene expression in humans |
title_sort | impact of sleep deprivation and nighttime light exposure on clock gene expression in humans |
topic | Clinical Science |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3195968/ https://www.ncbi.nlm.nih.gov/pubmed/21990077 http://dx.doi.org/10.3325/cmj.2011.52.594 |
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