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dc.contributor.author
Barrionuevo, Pablo Alejandro  
dc.contributor.author
Nicandro, Nathaniel  
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McAnany, J. Jason  
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Zele, Andrew J.  
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Gamlin, Paul  
dc.contributor.author
Cao, Dingcai  
dc.date.available
2017-01-26T19:38:08Z  
dc.date.issued
2014-02  
dc.identifier.citation
Barrionuevo, Pablo Alejandro; Nicandro, Nathaniel; McAnany, J. Jason; Zele, Andrew J.; Gamlin, Paul; et al.; Assessing Rod, Cone, and Melanopsin Contributions to Human Pupil Flicker Responses; Association for Research in Vision and Ophthalmology; Investigative Ophthalmology & Visual Science; 55; 2; 2-2014; 719-727  
dc.identifier.issn
0146-0404  
dc.identifier.uri
http://hdl.handle.net/11336/12007  
dc.description.abstract
Purpose: To determine the relative contributions of rods, cones and melanopsin to pupil responses in humans using temporal sinusoidal stimulation for light levels spanning the low mesopic to photopic range. Methods: A four-primary Ganzfeld photostimulator controlled flicker stimulations at seven light levels (-2.7 to 2 log cd/m2) and five frequencies (0.5 to 8Hz). Pupil diameter was measured using a high-resolution eyetracker. Three kinds of sinusoidal photoreceptor modulations were generated using silent substitution: 1) rod modulation, 2) cone modulation, and 3) combined rod and cone modulation in phase (Experiment 1) or phase shifted (Experiment 2) from a fixed rod phase. The melanopsin excitation was computed for each condition. A vector sum model was used to estimate the relative contribution of rods, cones and melanopsin to the pupil response. Results: From Experiment 1, the pupil frequency response peaked at 1Hz at two mesopic light levels for the three modulation conditions. Analyzing the rod-cone phase difference for the combined modulations (Experiment 2) identified a V-shaped response amplitude with a minimum between 135° and 180°. The pupil response phases increased as cone modulation phase increased. The pupil amplitude increased with increasing light level for cone and combined in-phase rod and cone modulation, but not for the rod modulation. Conclusions: These results demonstrate that cone- and rod-pathway contributions are more predominant than melanopsin contribution to the phasic pupil response. The combined rod, cone and melanopsin inputs to the phasic state of the pupil light reflex follow linear summation.  
dc.format
application/pdf  
dc.language.iso
eng  
dc.publisher
Association for Research in Vision and Ophthalmology  
dc.rights
info:eu-repo/semantics/openAccess  
dc.rights.uri
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/  
dc.subject
Melanopsin  
dc.subject
Flicker  
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Silent-Substitution  
dc.subject
Pupil Light Reflex  
dc.subject.classification
Neurociencias  
dc.subject.classification
Medicina Básica  
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CIENCIAS MÉDICAS Y DE LA SALUD  
dc.title
Assessing Rod, Cone, and Melanopsin Contributions to Human Pupil Flicker Responses  
dc.type
info:eu-repo/semantics/article  
dc.type
info:ar-repo/semantics/artículo  
dc.type
info:eu-repo/semantics/publishedVersion  
dc.date.updated
2017-01-24T18:32:04Z  
dc.identifier.eissn
1552-5783  
dc.journal.volume
55  
dc.journal.number
2  
dc.journal.pagination
719-727  
dc.journal.pais
Estados Unidos  
dc.journal.ciudad
Rockville  
dc.description.fil
Fil: Barrionuevo, Pablo Alejandro. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Tucuman. Instituto de Investigacion En Luz, Ambiente y Vision; Argentina. University Of Illinois; Estados Unidos  
dc.description.fil
Fil: Nicandro, Nathaniel. University Of Illinois; Estados Unidos  
dc.description.fil
Fil: McAnany, J. Jason. University Of Illinois; Estados Unidos  
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Fil: Zele, Andrew J.. University Of Queensland; Australia  
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Fil: Gamlin, Paul. University Of Alabama At Birmingahm; Estados Unidos  
dc.description.fil
Fil: Cao, Dingcai. University Of Illinois; Estados Unidos  
dc.journal.title
Investigative Ophthalmology & Visual Science  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/url/http://iovs.arvojournals.org/article.aspx?articleid=2189826  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1167/iovs.13-13252  
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info:eu-repo/semantics/altIdentifier/url/https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3915766/