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Preliminary evidence that light through the eyelids can suppress melatonin and phase shift dim light melatonin onset
BACKGROUND: A previous study reported a method for measuring the spectral transmittance of individual human eyelids. A prototype light mask using narrow-band “green” light (λ(max) = 527 nm) was used to deliver light through closed eyelids in two within-subjects studies. The first study investigated...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3469368/ https://www.ncbi.nlm.nih.gov/pubmed/22564396 http://dx.doi.org/10.1186/1756-0500-5-221 |
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author | Figueiro, Mariana G Rea, Mark S |
author_facet | Figueiro, Mariana G Rea, Mark S |
author_sort | Figueiro, Mariana G |
collection | PubMed |
description | BACKGROUND: A previous study reported a method for measuring the spectral transmittance of individual human eyelids. A prototype light mask using narrow-band “green” light (λ(max) = 527 nm) was used to deliver light through closed eyelids in two within-subjects studies. The first study investigated whether an individual-specific light dose could suppress melatonin by 40% through the closed eyelid without disrupting sleep. The light doses were delivered at three times during the night: 1) beginning (while subjects were awake), 2) middle (during rapid eye movement (REM) sleep), and 3) end (during non-REM sleep). The second study investigated whether two individual-specific light doses expected to suppress melatonin by 30% and 60% and delivered through subjects’ closed eyelids before the time of their predicted minimum core body temperature would phase delay the timing of their dim light melatonin onset (DLMO). FINDINGS: Compared to a dark control night, light delivered through eyelids suppressed melatonin by 36% (p = 0.01) after 60-minute light exposure at the beginning, 45% (p = 0.01) at the middle, and 56% (p < 0.0001) at the end of the night. In the second study, compared to a dark control night, melatonin was suppressed by 25% (p = 0.03) and by 45% (p = 0.009) and circadian phase, as measured by DLMO, was delayed by 17 minutes (p = 0.03) and 71 minutes (ns) after 60-minute exposures to light levels 1 and 2, respectively. CONCLUSIONS: These studies demonstrate that individual-specific doses of light delivered through closed eyelids can suppress melatonin and phase shift DLMO and may be used to treat circadian sleep disorders. |
format | Online Article Text |
id | pubmed-3469368 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-34693682012-10-12 Preliminary evidence that light through the eyelids can suppress melatonin and phase shift dim light melatonin onset Figueiro, Mariana G Rea, Mark S BMC Res Notes Short Report BACKGROUND: A previous study reported a method for measuring the spectral transmittance of individual human eyelids. A prototype light mask using narrow-band “green” light (λ(max) = 527 nm) was used to deliver light through closed eyelids in two within-subjects studies. The first study investigated whether an individual-specific light dose could suppress melatonin by 40% through the closed eyelid without disrupting sleep. The light doses were delivered at three times during the night: 1) beginning (while subjects were awake), 2) middle (during rapid eye movement (REM) sleep), and 3) end (during non-REM sleep). The second study investigated whether two individual-specific light doses expected to suppress melatonin by 30% and 60% and delivered through subjects’ closed eyelids before the time of their predicted minimum core body temperature would phase delay the timing of their dim light melatonin onset (DLMO). FINDINGS: Compared to a dark control night, light delivered through eyelids suppressed melatonin by 36% (p = 0.01) after 60-minute light exposure at the beginning, 45% (p = 0.01) at the middle, and 56% (p < 0.0001) at the end of the night. In the second study, compared to a dark control night, melatonin was suppressed by 25% (p = 0.03) and by 45% (p = 0.009) and circadian phase, as measured by DLMO, was delayed by 17 minutes (p = 0.03) and 71 minutes (ns) after 60-minute exposures to light levels 1 and 2, respectively. CONCLUSIONS: These studies demonstrate that individual-specific doses of light delivered through closed eyelids can suppress melatonin and phase shift DLMO and may be used to treat circadian sleep disorders. BioMed Central 2012-05-07 /pmc/articles/PMC3469368/ /pubmed/22564396 http://dx.doi.org/10.1186/1756-0500-5-221 Text en Copyright ©2012 Figueiro and Rea; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Short Report Figueiro, Mariana G Rea, Mark S Preliminary evidence that light through the eyelids can suppress melatonin and phase shift dim light melatonin onset |
title | Preliminary evidence that light through the eyelids can suppress melatonin and phase shift dim light melatonin onset |
title_full | Preliminary evidence that light through the eyelids can suppress melatonin and phase shift dim light melatonin onset |
title_fullStr | Preliminary evidence that light through the eyelids can suppress melatonin and phase shift dim light melatonin onset |
title_full_unstemmed | Preliminary evidence that light through the eyelids can suppress melatonin and phase shift dim light melatonin onset |
title_short | Preliminary evidence that light through the eyelids can suppress melatonin and phase shift dim light melatonin onset |
title_sort | preliminary evidence that light through the eyelids can suppress melatonin and phase shift dim light melatonin onset |
topic | Short Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3469368/ https://www.ncbi.nlm.nih.gov/pubmed/22564396 http://dx.doi.org/10.1186/1756-0500-5-221 |
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