Evidence map›Paper›PMID 27276063›Full record

ArticlePLoS biology2016

Melanopsin Regulates Both Sleep-Promoting and Arousal-Promoting Responses to Light.

Violetta Pilorz, Shu K E Tam, Steven Hughes, Carina A Pothecary, Aarti Jagannath, Mark W Hankins, David M Bannerman, Stafford L Lightman, Vladyslav V Vyazovskiy, Patrick M Nolan and 2 more

Open access · goldAbstract read
In one paragraph

Article in PLoS biology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 97 papers.

0numbers the graph read from it
0cells of the map it votes in
97citing papers in PubMed
9.3field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

97 citing papers in PubMed, 169 citations in OpenAlex.

  1. A day sleep promoting role of phototransduction inNeurobiology of sleep and circadian rhythms · 2026
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37 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors at 3 institutions in 1 country.

Violetta PilorzSleep and Circadian Neuroscience Institute (SCNi), Nuffield Department of Clinical Neurosciences, Oxford Molecular Pathology Institute, Dunn School of Pathology, University of Oxford, Oxford, United Kingdom.ORCID 0000-0003-0474-8975
Shu K E TamSleep and Circadian Neuroscience Institute (SCNi), Nuffield Department of Clinical Neurosciences, Oxford Molecular Pathology Institute, Dunn School of Pathology, University of Oxford, Oxford, United Kingdom.
Steven HughesSleep and Circadian Neuroscience Institute (SCNi), Nuffield Department of Clinical Neurosciences, Oxford Molecular Pathology Institute, Dunn School of Pathology, University of Oxford, Oxford, United Kingdom.
Carina A PothecarySleep and Circadian Neuroscience Institute (SCNi), Nuffield Department of Clinical Neurosciences, Oxford Molecular Pathology Institute, Dunn School of Pathology, University of Oxford, Oxford, United Kingdom.ORCID 0000-0001-8759-9404
Aarti JagannathSleep and Circadian Neuroscience Institute (SCNi), Nuffield Department of Clinical Neurosciences, Oxford Molecular Pathology Institute, Dunn School of Pathology, University of Oxford, Oxford, United Kingdom.
Mark W HankinsSleep and Circadian Neuroscience Institute (SCNi), Nuffield Department of Clinical Neurosciences, Oxford Molecular Pathology Institute, Dunn School of Pathology, University of Oxford, Oxford, United Kingdom.
David M BannermanDepartment of Experimental Psychology, University of Oxford, Oxford, United Kingdom.
Stafford L LightmanHenry Wellcome Laboratories for Integrative Neuroscience and Endocrinology, University of Bristol, Bristol, United Kingdom.
Vladyslav V VyazovskiyDepartment of Physiology, Anatomy and Genetics, University of Oxford, Oxford, United Kingdom.
Patrick M NolanMRC Harwell, Harwell Science and Innovation Campus, Oxfordshire, United Kingdom.
Russell G FosterSleep and Circadian Neuroscience Institute (SCNi), Nuffield Department of Clinical Neurosciences, Oxford Molecular Pathology Institute, Dunn School of Pathology, University of Oxford, Oxford, United Kingdom.
Stuart N PeirsonSleep and Circadian Neuroscience Institute (SCNi), Nuffield Department of Clinical Neurosciences, Oxford Molecular Pathology Institute, Dunn School of Pathology, University of Oxford, Oxford, United Kingdom.
University of Oxford · GBMary Lyon Centre at MRC Harwell · GBUniversity of Bristol · GB

Funding

Biotechnology and Biological Sciences Research Council BB/I021086/1Medical Research Council MC_U142684173Wellcome TrustWellcome Trust 098461/Z/12/Z
6 · The paper itself

Abstract

Light plays a critical role in the regulation of numerous aspects of physiology and behaviour, including the entrainment of circadian rhythms and the regulation of sleep. These responses involve melanopsin (OPN4)-expressing photosensitive retinal ganglion cells (pRGCs) in addition to rods and cones. Nocturnal light exposure in rodents has been shown to result in rapid sleep induction, in which melanopsin plays a key role. However, studies have also shown that light exposure can result in elevated corticosterone, a response that is not compatible with sleep. To investigate these contradictory findings and to dissect the relative contribution of pRGCs and rods/cones, we assessed the effects of light of different wavelengths on behaviourally defined sleep. Here, we show that blue light (470 nm) causes behavioural arousal, elevating corticosterone and delaying sleep onset. By contrast, green light (530 nm) produces rapid sleep induction. Compared to wildtype mice, these responses are altered in melanopsin-deficient mice (Opn4-/-), resulting in enhanced sleep in response to blue light but delayed sleep induction in response to green or white light. We go on to show that blue light evokes higher Fos induction in the SCN compared to the sleep-promoting ventrolateral preoptic area (VLPO), whereas green light produced greater responses in the VLPO. Collectively, our data demonstrates that nocturnal light exposure can have either an arousal- or sleep-promoting effect, and that these responses are melanopsin-mediated via different neural pathways with different spectral sensitivities. These findings raise important questions relating to how artificial light may alter behaviour in both the work and domestic setting.

Indexed as

LightAnimalsArousalCorticosteroneGene ExpressionMelanopsinMice, Inbred C57BLMice, KnockoutModels, BiologicalPeriod Circadian ProteinsPhotoreceptor Cells, VertebratePreoptic AreaProto-Oncogene Proteins c-fosRetinal Ganglion CellsRod OpsinsSleepCorticosteroneMelanopsinPer1 protein, mousePer2 protein, mousePeriod Circadian ProteinsProto-Oncogene Proteins c-fosRod Opsins

Identifiers

PMID27276063
PMCPMC4898879
OpenAlexW2415509130

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.