Evidence map›Paper›PMID 29311335›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2018

Melanopsin- and L-cone-induced pupil constriction is inhibited by S- and M-cones in humans.

Tom Woelders, Thomas Leenheers, Marijke C M Gordijn, Roelof A Hut, Domien G M Beersma, Emma J Wams

Erratum issuedOpen access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
4.9field-weighted citation impact, top 4% 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

41 citing papers in PubMed, 84 citations in OpenAlex.

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  11. Human-Centric Lighting Research and Policy in the Melanopsin Age.Policy insights from the behavioral and brain sciences · 2023
    Article
  12. Article
  13. Circadian rhythm entrainment of the jewel wasp,Proceedings. Biological sciences · 2023
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  15. Review
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  19. The Effect of Refractive Error on Melanopsin-Driven Pupillary Responses.Investigative ophthalmology & visual science · 2020
    Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 1 institution in 1 country.

Tom WoeldersChronobiology Unit, Groningen Institute for Evolutionary Life Sciences, 9700CC Groningen, The Netherlands; t.woelders@rug.nl.
Thomas LeenheersChronobiology Unit, Groningen Institute for Evolutionary Life Sciences, 9700CC Groningen, The Netherlands.
Marijke C M GordijnChronobiology Unit, Groningen Institute for Evolutionary Life Sciences, 9700CC Groningen, The Netherlands.
Roelof A HutChronobiology Unit, Groningen Institute for Evolutionary Life Sciences, 9700CC Groningen, The Netherlands.
Domien G M BeersmaChronobiology Unit, Groningen Institute for Evolutionary Life Sciences, 9700CC Groningen, The Netherlands.
Emma J WamsChronobiology Unit, Groningen Institute for Evolutionary Life Sciences, 9700CC Groningen, The Netherlands.
University of Groningen · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The human retina contains five photoreceptor types: rods; short (S)-, mid (M)-, and long (L)-wavelength-sensitive cones; and melanopsin-expressing ganglion cells. Recently, it has been shown that selective increments in M-cone activation are paradoxically perceived as brightness decrements, as opposed to L-cone increments. Here we show that similar effects are also observed in the pupillary light response, whereby M-cone or S-cone increments lead to pupil dilation whereas L-cone or melanopic illuminance increments resulted in pupil constriction. Additionally, intermittent photoreceptor activation increased pupil constriction over a 30-min interval. Modulation of L-cone or melanopic illuminance within the 0.25-4-Hz frequency range resulted in more sustained pupillary constriction than light of constant intensity. Opposite results were found for S-cone and M-cone modulations (2 Hz), mirroring the dichotomy observed in the transient responses. The transient and sustained pupillary light responses therefore suggest that S- and M-cones provide inhibitory input to the pupillary control system when selectively activated, whereas L-cones and melanopsin response fulfill an excitatory role. These findings provide insight into functional networks in the human retina and the effect of color-coding in nonvisual responses to light, and imply that nonvisual and visual brightness discrimination may share a common pathway that starts in the retina.

Indexed as

AdultFemaleHumansMalePupilRetinal Cone Photoreceptor CellsVisual PerceptionYoung Adultconeshuman pupillary light responseipRGCmelanopsinsilent substitution

Identifiers

PMID29311335
PMCPMC5789936
OpenAlexW2783769528

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.