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Dim light in the evening causes coordinated realignment of circadian rhythms, sleep, and short-term memory
Light provides the primary signal for entraining circadian rhythms to the day/night cycle. In addition to rods and cones, the retina contains a small population of photosensitive retinal ganglion cells (pRGCs) expressing the photopigment melanopsin (OPN4). Concerns have been raised that exposure to...
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Published in: | Proceedings of the National Academy of Sciences - PNAS 2021-09, Vol.118 (39), p.1-12 |
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creator | Tam, Shu K. E. Brown, Laurence A. Wilson, Tatiana S. Tir, Selma Fisk, Angus S. Pothecary, Carina A. van der Vinne, Vincent Foster, Russell G. Vyazovskiy, Vladyslav V. Bannerman, David M. Harrington, Mary E. Peirson, Stuart N. |
description | Light provides the primary signal for entraining circadian rhythms to the day/night cycle. In addition to rods and cones, the retina contains a small population of photosensitive retinal ganglion cells (pRGCs) expressing the photopigment melanopsin (OPN4). Concerns have been raised that exposure to dim artificial lighting in the evening (DLE) may perturb circadian rhythms and sleep patterns, and OPN4 is presumed to mediate these effects. Here, we examine the effects of 4-h, 20-lux DLE on circadian physiology and behavior in mice and the role of OPN4 in these responses. We show that 2 wk of DLE induces a phase delay of ∼2 to 3 h in mice, comparable to that reported in humans. DLE-induced phase shifts are unaffected in Opn4
−/− mice, indicating that rods and cones are capable of driving these responses in the absence of melanopsin. DLE delays molecular clock rhythms in the heart, liver, adrenal gland, and dorsal hippocampus. It also reverses short-term recognition memory performance, which is associated with changes in preceding sleep history. In addition, DLE modifies patterns of hypothalamic and cortical cFos signals, a molecular correlate of recent neuronal activity. Together, our data show that DLE causes coordinated realignment of circadian rhythms, sleep patterns, and short-term memory process in mice. These effects are particularly relevant as DLE conditions―due to artificial light exposure―are experienced by the majority of the populace on a daily basis. |
doi_str_mv | 10.1073/pnas.2101591118 |
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−/− mice, indicating that rods and cones are capable of driving these responses in the absence of melanopsin. DLE delays molecular clock rhythms in the heart, liver, adrenal gland, and dorsal hippocampus. It also reverses short-term recognition memory performance, which is associated with changes in preceding sleep history. In addition, DLE modifies patterns of hypothalamic and cortical cFos signals, a molecular correlate of recent neuronal activity. Together, our data show that DLE causes coordinated realignment of circadian rhythms, sleep patterns, and short-term memory process in mice. These effects are particularly relevant as DLE conditions―due to artificial light exposure―are experienced by the majority of the populace on a daily basis.</description><identifier>ISSN: 0027-8424</identifier><identifier>EISSN: 1091-6490</identifier><identifier>DOI: 10.1073/pnas.2101591118</identifier><identifier>PMID: 34556572</identifier><language>eng</language><publisher>Washington: National Academy of Sciences</publisher><subject>Adrenal glands ; Biological Sciences ; Circadian rhythm ; Circadian rhythms ; Cognitive ability ; Cones ; Exposure ; Hypothalamus ; Melanopsin ; Photosensitivity ; Realignment ; Retina ; Retinal ganglion cells ; Rods ; Short term memory ; Sleep</subject><ispartof>Proceedings of the National Academy of Sciences - PNAS, 2021-09, Vol.118 (39), p.1-12</ispartof><rights>Copyright National Academy of Sciences Sep 28, 2021</rights><rights>Copyright © 2021 the Author(s). Published by PNAS. 2021</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c466t-a4955d4bcae2d71d2146c47ad3755e1630a36e6b2405e537125c851df10e7023</citedby><cites>FETCH-LOGICAL-c466t-a4955d4bcae2d71d2146c47ad3755e1630a36e6b2405e537125c851df10e7023</cites><orcidid>0000-0001-8116-4100 ; 0000-0003-2266-6455 ; 0000-0001-5469-4544 ; 0000-0002-4336-6681 ; 0000-0003-3653-834X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/27075868$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/27075868$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793,58238,58471</link.rule.ids></links><search><creatorcontrib>Tam, Shu K. E.</creatorcontrib><creatorcontrib>Brown, Laurence A.</creatorcontrib><creatorcontrib>Wilson, Tatiana S.</creatorcontrib><creatorcontrib>Tir, Selma</creatorcontrib><creatorcontrib>Fisk, Angus S.</creatorcontrib><creatorcontrib>Pothecary, Carina A.</creatorcontrib><creatorcontrib>van der Vinne, Vincent</creatorcontrib><creatorcontrib>Foster, Russell G.</creatorcontrib><creatorcontrib>Vyazovskiy, Vladyslav V.</creatorcontrib><creatorcontrib>Bannerman, David M.</creatorcontrib><creatorcontrib>Harrington, Mary E.</creatorcontrib><creatorcontrib>Peirson, Stuart N.</creatorcontrib><title>Dim light in the evening causes coordinated realignment of circadian rhythms, sleep, and short-term memory</title><title>Proceedings of the National Academy of Sciences - PNAS</title><description>Light provides the primary signal for entraining circadian rhythms to the day/night cycle. In addition to rods and cones, the retina contains a small population of photosensitive retinal ganglion cells (pRGCs) expressing the photopigment melanopsin (OPN4). Concerns have been raised that exposure to dim artificial lighting in the evening (DLE) may perturb circadian rhythms and sleep patterns, and OPN4 is presumed to mediate these effects. Here, we examine the effects of 4-h, 20-lux DLE on circadian physiology and behavior in mice and the role of OPN4 in these responses. We show that 2 wk of DLE induces a phase delay of ∼2 to 3 h in mice, comparable to that reported in humans. DLE-induced phase shifts are unaffected in Opn4
−/− mice, indicating that rods and cones are capable of driving these responses in the absence of melanopsin. DLE delays molecular clock rhythms in the heart, liver, adrenal gland, and dorsal hippocampus. It also reverses short-term recognition memory performance, which is associated with changes in preceding sleep history. In addition, DLE modifies patterns of hypothalamic and cortical cFos signals, a molecular correlate of recent neuronal activity. Together, our data show that DLE causes coordinated realignment of circadian rhythms, sleep patterns, and short-term memory process in mice. These effects are particularly relevant as DLE conditions―due to artificial light exposure―are experienced by the majority of the populace on a daily basis.</description><subject>Adrenal glands</subject><subject>Biological Sciences</subject><subject>Circadian rhythm</subject><subject>Circadian rhythms</subject><subject>Cognitive ability</subject><subject>Cones</subject><subject>Exposure</subject><subject>Hypothalamus</subject><subject>Melanopsin</subject><subject>Photosensitivity</subject><subject>Realignment</subject><subject>Retina</subject><subject>Retinal ganglion cells</subject><subject>Rods</subject><subject>Short term memory</subject><subject>Sleep</subject><issn>0027-8424</issn><issn>1091-6490</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNpdkb1rHDEUxEVIiC-261QBQZoUXlvf0jYB43zYYEjjXuikd7c6dqWLpDXcf589zjgk1SvmN8M8BqGPlFxTovnNPrl6zSihsqeUmjdoRUlPOyV68hatCGG6M4KJM_Sh1h0hpJeGvEdnXEippGYrtPsWJzzG7dBwTLgNgOEZUkxb7N1coWKfcwkxuQYBF3ALmiZIDecN9rF4F6JLuAyHNkz1CtcRYH-FXQq4Drm0rkGZ8ARTLocL9G7jxgqXL_ccPf34_nR33z3--vlwd_vYeaFU65zopQxi7R2woGlgVCgvtAtcSwlUceK4ArVmgkiQXFMmvZE0bCgBTRg_R19Psft5PUHwS9niRrsvcXLlYLOL9l8lxcFu87M1whil-BLw5SWg5N8z1GanWD2Mo0uQ52qZ1EpJpZlY0M__obs8l7R8d6R6ynvKyELdnChfcq0FNq9lKLHHGe1xRvt3xsXx6eTY1ZbLK8400dIow_8A0_6Zsg</recordid><startdate>20210928</startdate><enddate>20210928</enddate><creator>Tam, Shu K. 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E.</au><au>Brown, Laurence A.</au><au>Wilson, Tatiana S.</au><au>Tir, Selma</au><au>Fisk, Angus S.</au><au>Pothecary, Carina A.</au><au>van der Vinne, Vincent</au><au>Foster, Russell G.</au><au>Vyazovskiy, Vladyslav V.</au><au>Bannerman, David M.</au><au>Harrington, Mary E.</au><au>Peirson, Stuart N.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Dim light in the evening causes coordinated realignment of circadian rhythms, sleep, and short-term memory</atitle><jtitle>Proceedings of the National Academy of Sciences - PNAS</jtitle><date>2021-09-28</date><risdate>2021</risdate><volume>118</volume><issue>39</issue><spage>1</spage><epage>12</epage><pages>1-12</pages><issn>0027-8424</issn><eissn>1091-6490</eissn><abstract>Light provides the primary signal for entraining circadian rhythms to the day/night cycle. In addition to rods and cones, the retina contains a small population of photosensitive retinal ganglion cells (pRGCs) expressing the photopigment melanopsin (OPN4). Concerns have been raised that exposure to dim artificial lighting in the evening (DLE) may perturb circadian rhythms and sleep patterns, and OPN4 is presumed to mediate these effects. Here, we examine the effects of 4-h, 20-lux DLE on circadian physiology and behavior in mice and the role of OPN4 in these responses. We show that 2 wk of DLE induces a phase delay of ∼2 to 3 h in mice, comparable to that reported in humans. DLE-induced phase shifts are unaffected in Opn4
−/− mice, indicating that rods and cones are capable of driving these responses in the absence of melanopsin. DLE delays molecular clock rhythms in the heart, liver, adrenal gland, and dorsal hippocampus. It also reverses short-term recognition memory performance, which is associated with changes in preceding sleep history. In addition, DLE modifies patterns of hypothalamic and cortical cFos signals, a molecular correlate of recent neuronal activity. Together, our data show that DLE causes coordinated realignment of circadian rhythms, sleep patterns, and short-term memory process in mice. These effects are particularly relevant as DLE conditions―due to artificial light exposure―are experienced by the majority of the populace on a daily basis.</abstract><cop>Washington</cop><pub>National Academy of Sciences</pub><pmid>34556572</pmid><doi>10.1073/pnas.2101591118</doi><tpages>12</tpages><orcidid>https://orcid.org/0000-0001-8116-4100</orcidid><orcidid>https://orcid.org/0000-0003-2266-6455</orcidid><orcidid>https://orcid.org/0000-0001-5469-4544</orcidid><orcidid>https://orcid.org/0000-0002-4336-6681</orcidid><orcidid>https://orcid.org/0000-0003-3653-834X</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Adrenal glands Biological Sciences Circadian rhythm Circadian rhythms Cognitive ability Cones Exposure Hypothalamus Melanopsin Photosensitivity Realignment Retina Retinal ganglion cells Rods Short term memory Sleep |
title | Dim light in the evening causes coordinated realignment of circadian rhythms, sleep, and short-term memory |
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