Optimizing Light Flash Sequence Duration to Shift Human Circadian Phase
Unlike light input for forming images, non-image-forming retinal pathways are optimized to convey information about the total light environment, integrating this information over time and space. In a variety of species, discontinuous light sequences (flashes) can be effective stimuli, notably impact...
| 发表在: | Biology |
|---|---|
| Main Authors: | , , |
| 格式: | 文件 |
| 语言: | 英语 |
| 出版: |
MDPI AG
2022-12-01
|
| 主题: | |
| 在线阅读: | https://www.mdpi.com/2079-7737/11/12/1807 |
| _version_ | 1850476079655944192 |
|---|---|
| author | Daniel S. Joyce Manuel Spitschan Jamie M. Zeitzer |
| author_facet | Daniel S. Joyce Manuel Spitschan Jamie M. Zeitzer |
| author_sort | Daniel S. Joyce |
| collection | DOAJ |
| container_title | Biology |
| description | Unlike light input for forming images, non-image-forming retinal pathways are optimized to convey information about the total light environment, integrating this information over time and space. In a variety of species, discontinuous light sequences (flashes) can be effective stimuli, notably impacting circadian entrainment. In this study, we examined the extent to which this temporal integration can occur. A group of healthy, young (<i>n</i> = 20) individuals took part in a series of 16-day protocols in which we examined the impact of different lengths of light flash sequences on circadian timing. We find a significant phase change of −0.70 h in response to flashes that did not differ by duration; a 15-min sequence could engender as much change in circadian timing as 3.5-h sequences. Acute suppression of melatonin was also observed during short (15-min) exposures, but not in exposures over one hour in length. Our data are consistent with the theory that responses to light flashes are mediated by the extrinsic, rod/cone pathway, and saturate the response of this pathway within 15 min. Further excitation leads to no greater change in circadian timing and an inability to acutely suppress melatonin, indicating that this pathway may be in a refractory state following this brief light stimulation. |
| format | Article |
| id | doaj-art-e2c1dcc3e02c42b795293c9d5ed9d7c5 |
| institution | Directory of Open Access Journals |
| issn | 2079-7737 |
| language | English |
| publishDate | 2022-12-01 |
| publisher | MDPI AG |
| record_format | Article |
| spelling | doaj-art-e2c1dcc3e02c42b795293c9d5ed9d7c52025-08-19T22:39:42ZengMDPI AGBiology2079-77372022-12-011112180710.3390/biology11121807Optimizing Light Flash Sequence Duration to Shift Human Circadian PhaseDaniel S. Joyce0Manuel Spitschan1Jamie M. Zeitzer2Department of Psychiatry and Behavioral Sciences, Stanford University, Stanford, CA 94305, USADepartment of Psychiatry and Behavioral Sciences, Stanford University, Stanford, CA 94305, USADepartment of Psychiatry and Behavioral Sciences, Stanford University, Stanford, CA 94305, USAUnlike light input for forming images, non-image-forming retinal pathways are optimized to convey information about the total light environment, integrating this information over time and space. In a variety of species, discontinuous light sequences (flashes) can be effective stimuli, notably impacting circadian entrainment. In this study, we examined the extent to which this temporal integration can occur. A group of healthy, young (<i>n</i> = 20) individuals took part in a series of 16-day protocols in which we examined the impact of different lengths of light flash sequences on circadian timing. We find a significant phase change of −0.70 h in response to flashes that did not differ by duration; a 15-min sequence could engender as much change in circadian timing as 3.5-h sequences. Acute suppression of melatonin was also observed during short (15-min) exposures, but not in exposures over one hour in length. Our data are consistent with the theory that responses to light flashes are mediated by the extrinsic, rod/cone pathway, and saturate the response of this pathway within 15 min. Further excitation leads to no greater change in circadian timing and an inability to acutely suppress melatonin, indicating that this pathway may be in a refractory state following this brief light stimulation.https://www.mdpi.com/2079-7737/11/12/1807circadian rhythmlightmelatoninsleepdim light melatonin onsetflash |
| spellingShingle | Daniel S. Joyce Manuel Spitschan Jamie M. Zeitzer Optimizing Light Flash Sequence Duration to Shift Human Circadian Phase circadian rhythm light melatonin sleep dim light melatonin onset flash |
| title | Optimizing Light Flash Sequence Duration to Shift Human Circadian Phase |
| title_full | Optimizing Light Flash Sequence Duration to Shift Human Circadian Phase |
| title_fullStr | Optimizing Light Flash Sequence Duration to Shift Human Circadian Phase |
| title_full_unstemmed | Optimizing Light Flash Sequence Duration to Shift Human Circadian Phase |
| title_short | Optimizing Light Flash Sequence Duration to Shift Human Circadian Phase |
| title_sort | optimizing light flash sequence duration to shift human circadian phase |
| topic | circadian rhythm light melatonin sleep dim light melatonin onset flash |
| url | https://www.mdpi.com/2079-7737/11/12/1807 |
| work_keys_str_mv | AT danielsjoyce optimizinglightflashsequencedurationtoshifthumancircadianphase AT manuelspitschan optimizinglightflashsequencedurationtoshifthumancircadianphase AT jamiemzeitzer optimizinglightflashsequencedurationtoshifthumancircadianphase |
