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Modulation of recognition memory performance by light requires both melanopsin and classical photoreceptors
Acute light exposure exerts various effects on physiology and behaviour. Although the effects of light on brain network activity in humans are well demonstrated, the effects of light on cognitive performance are inconclusive, with the size, as well as direction, of the effect depending on the nature...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5204172/ https://www.ncbi.nlm.nih.gov/pubmed/28003454 http://dx.doi.org/10.1098/rspb.2016.2275 |
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author | Tam, Shu K. E. Hasan, Sibah Hughes, Steven Hankins, Mark W. Foster, Russell G. Bannerman, David M. Peirson, Stuart N. |
author_facet | Tam, Shu K. E. Hasan, Sibah Hughes, Steven Hankins, Mark W. Foster, Russell G. Bannerman, David M. Peirson, Stuart N. |
author_sort | Tam, Shu K. E. |
collection | PubMed |
description | Acute light exposure exerts various effects on physiology and behaviour. Although the effects of light on brain network activity in humans are well demonstrated, the effects of light on cognitive performance are inconclusive, with the size, as well as direction, of the effect depending on the nature of the task. Similarly, in nocturnal rodents, bright light can either facilitate or disrupt performance depending on the type of task employed. Crucially, it is unclear whether the effects of light on behavioural performance are mediated via the classical image-forming rods and cones or the melanopsin-expressing photosensitive retinal ganglion cells. Here, we investigate the modulatory effects of light on memory performance in mice using the spontaneous object recognition task. Importantly, we examine which photoreceptors are required to mediate the effects of light on memory performance. By using a cross-over design, we show that object recognition memory is disrupted when the test phase is conducted under a bright light (350 lux), regardless of the light level in the sample phase (10 or 350 lux), demonstrating that exposure to a bright light at the time of test, rather than at the time of encoding, impairs performance. Strikingly, the modulatory effect of light on memory performance is completely abolished in both melanopsin-deficient and rodless–coneless mice. Our findings provide direct evidence that melanopsin-driven and rod/cone-driven photoresponses are integrated in order to mediate the effect of light on memory performance. |
format | Online Article Text |
id | pubmed-5204172 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | The Royal Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-52041722017-01-05 Modulation of recognition memory performance by light requires both melanopsin and classical photoreceptors Tam, Shu K. E. Hasan, Sibah Hughes, Steven Hankins, Mark W. Foster, Russell G. Bannerman, David M. Peirson, Stuart N. Proc Biol Sci Research Articles Acute light exposure exerts various effects on physiology and behaviour. Although the effects of light on brain network activity in humans are well demonstrated, the effects of light on cognitive performance are inconclusive, with the size, as well as direction, of the effect depending on the nature of the task. Similarly, in nocturnal rodents, bright light can either facilitate or disrupt performance depending on the type of task employed. Crucially, it is unclear whether the effects of light on behavioural performance are mediated via the classical image-forming rods and cones or the melanopsin-expressing photosensitive retinal ganglion cells. Here, we investigate the modulatory effects of light on memory performance in mice using the spontaneous object recognition task. Importantly, we examine which photoreceptors are required to mediate the effects of light on memory performance. By using a cross-over design, we show that object recognition memory is disrupted when the test phase is conducted under a bright light (350 lux), regardless of the light level in the sample phase (10 or 350 lux), demonstrating that exposure to a bright light at the time of test, rather than at the time of encoding, impairs performance. Strikingly, the modulatory effect of light on memory performance is completely abolished in both melanopsin-deficient and rodless–coneless mice. Our findings provide direct evidence that melanopsin-driven and rod/cone-driven photoresponses are integrated in order to mediate the effect of light on memory performance. The Royal Society 2016-12-28 /pmc/articles/PMC5204172/ /pubmed/28003454 http://dx.doi.org/10.1098/rspb.2016.2275 Text en © 2016 The Authors. http://creativecommons.org/licenses/by/4.0/ Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/, which permits unrestricted use, provided the original author and source are credited. |
spellingShingle | Research Articles Tam, Shu K. E. Hasan, Sibah Hughes, Steven Hankins, Mark W. Foster, Russell G. Bannerman, David M. Peirson, Stuart N. Modulation of recognition memory performance by light requires both melanopsin and classical photoreceptors |
title | Modulation of recognition memory performance by light requires both melanopsin and classical photoreceptors |
title_full | Modulation of recognition memory performance by light requires both melanopsin and classical photoreceptors |
title_fullStr | Modulation of recognition memory performance by light requires both melanopsin and classical photoreceptors |
title_full_unstemmed | Modulation of recognition memory performance by light requires both melanopsin and classical photoreceptors |
title_short | Modulation of recognition memory performance by light requires both melanopsin and classical photoreceptors |
title_sort | modulation of recognition memory performance by light requires both melanopsin and classical photoreceptors |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5204172/ https://www.ncbi.nlm.nih.gov/pubmed/28003454 http://dx.doi.org/10.1098/rspb.2016.2275 |
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