A five-Primary photostimulator suitable for studying intrinsically photosensitive retinal ganglion cell functions in humans

Autores
Cao, Dingcai; Nicandro, Nathaniel; Barrionuevo, Pablo Alejandro
Año de publicación
2015
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
Intrinsically photosensitive retinal ganglion cells (ipRGCs) can respond to light directly through self-contained photopigment, melanopsin. IpRGCs also receive inputs from rods and cones. Thus, studying ipRGC functions requires a novel photostimulating method that can account for all of the photoreceptor inputs. Here, we introduce an inexpensive LED-based five-primary photostimulator that can control the excitations of rods, S-, M-, L-cones and melanopsin-containing ipRGCs in humans at constant background photoreceptor excitation levels, a critical requirement for studying the adaptation behavior of ipRGCs with rod, cone or melanopsin input. We describe the theory and technical aspects (including optics, electronics, software and calibration) of the five-primary photostimulator. Then we present two preliminary studies using the photostimulator we have implemented to measure melanopsin-mediated pupil responses and temporal contrast sensitivity function (TCSF). The results showed that the S-cone input to pupil responses was antagonistic to the L-, M- or melanopsin inputs, consistent with an S-OFF and (L+M)-ON response property of primate ipRGCs (Dacey et al., 2005). In addition, the melanopsin-mediated TCSF had a distinctive pattern compared with L+M or S-cone mediated TCSF. Other than control individual photoreceptor excitation independently, the five-primary photostimulator has the flexibility in presenting stimuli modulating any combination of photoreceptor excitations, which allows to study the mechanisms by which ipRGCs combine various photoreceptor inputs.
Fil: Cao, Dingcai. University Of Illinois; Estados Unidos
Fil: Nicandro, Nathaniel. University Of Illinois; Estados Unidos
Fil: Barrionuevo, Pablo Alejandro. University Of Illinois; Estados Unidos. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina
Materia
Five-Primary
Photoreceptors
Melanopsin
Nivel de accesibilidad
acceso abierto
Condiciones de uso
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
Repositorio
CONICET Digital (CONICET)
Institución
Consejo Nacional de Investigaciones Científicas y Técnicas
OAI Identificador
oai:ri.conicet.gov.ar:11336/10617

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network_acronym_str CONICETDig
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network_name_str CONICET Digital (CONICET)
spelling A five-Primary photostimulator suitable for studying intrinsically photosensitive retinal ganglion cell functions in humansCao, DingcaiNicandro, NathanielBarrionuevo, Pablo AlejandroFive-PrimaryPhotoreceptorsMelanopsinhttps://purl.org/becyt/ford/1.3https://purl.org/becyt/ford/1https://purl.org/becyt/ford/2.6https://purl.org/becyt/ford/2Intrinsically photosensitive retinal ganglion cells (ipRGCs) can respond to light directly through self-contained photopigment, melanopsin. IpRGCs also receive inputs from rods and cones. Thus, studying ipRGC functions requires a novel photostimulating method that can account for all of the photoreceptor inputs. Here, we introduce an inexpensive LED-based five-primary photostimulator that can control the excitations of rods, S-, M-, L-cones and melanopsin-containing ipRGCs in humans at constant background photoreceptor excitation levels, a critical requirement for studying the adaptation behavior of ipRGCs with rod, cone or melanopsin input. We describe the theory and technical aspects (including optics, electronics, software and calibration) of the five-primary photostimulator. Then we present two preliminary studies using the photostimulator we have implemented to measure melanopsin-mediated pupil responses and temporal contrast sensitivity function (TCSF). The results showed that the S-cone input to pupil responses was antagonistic to the L-, M- or melanopsin inputs, consistent with an S-OFF and (L+M)-ON response property of primate ipRGCs (Dacey et al., 2005). In addition, the melanopsin-mediated TCSF had a distinctive pattern compared with L+M or S-cone mediated TCSF. Other than control individual photoreceptor excitation independently, the five-primary photostimulator has the flexibility in presenting stimuli modulating any combination of photoreceptor excitations, which allows to study the mechanisms by which ipRGCs combine various photoreceptor inputs.Fil: Cao, Dingcai. University Of Illinois; Estados UnidosFil: Nicandro, Nathaniel. University Of Illinois; Estados UnidosFil: Barrionuevo, Pablo Alejandro. University Of Illinois; Estados Unidos. Consejo Nacional de Investigaciones Científicas y Técnicas; ArgentinaAssociation for Research in Vision and Ophthalmology2015-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/10617Cao, Dingcai; Nicandro, Nathaniel; Barrionuevo, Pablo Alejandro; A five-Primary photostimulator suitable for studying intrinsically photosensitive retinal ganglion cell functions in humans; Association for Research in Vision and Ophthalmology; Journal of Vision; 15; 27; 1-2015; 1-131534-7362enginfo:eu-repo/semantics/altIdentifier/url/http://jov.arvojournals.org/article.aspx?articleid=2213232info:eu-repo/semantics/altIdentifier/doi/10.1167/15.1.27info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-17T11:13:42Zoai:ri.conicet.gov.ar:11336/10617instacron:CONICETInstitucionalhttp://ri.conicet.gov.ar/Organismo científico-tecnológicoNo correspondehttp://ri.conicet.gov.ar/oai/requestdasensio@conicet.gov.ar; lcarlino@conicet.gov.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:34982025-09-17 11:13:43.029CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse
dc.title.none.fl_str_mv A five-Primary photostimulator suitable for studying intrinsically photosensitive retinal ganglion cell functions in humans
title A five-Primary photostimulator suitable for studying intrinsically photosensitive retinal ganglion cell functions in humans
spellingShingle A five-Primary photostimulator suitable for studying intrinsically photosensitive retinal ganglion cell functions in humans
Cao, Dingcai
Five-Primary
Photoreceptors
Melanopsin
title_short A five-Primary photostimulator suitable for studying intrinsically photosensitive retinal ganglion cell functions in humans
title_full A five-Primary photostimulator suitable for studying intrinsically photosensitive retinal ganglion cell functions in humans
title_fullStr A five-Primary photostimulator suitable for studying intrinsically photosensitive retinal ganglion cell functions in humans
title_full_unstemmed A five-Primary photostimulator suitable for studying intrinsically photosensitive retinal ganglion cell functions in humans
title_sort A five-Primary photostimulator suitable for studying intrinsically photosensitive retinal ganglion cell functions in humans
dc.creator.none.fl_str_mv Cao, Dingcai
Nicandro, Nathaniel
Barrionuevo, Pablo Alejandro
author Cao, Dingcai
author_facet Cao, Dingcai
Nicandro, Nathaniel
Barrionuevo, Pablo Alejandro
author_role author
author2 Nicandro, Nathaniel
Barrionuevo, Pablo Alejandro
author2_role author
author
dc.subject.none.fl_str_mv Five-Primary
Photoreceptors
Melanopsin
topic Five-Primary
Photoreceptors
Melanopsin
purl_subject.fl_str_mv https://purl.org/becyt/ford/1.3
https://purl.org/becyt/ford/1
https://purl.org/becyt/ford/2.6
https://purl.org/becyt/ford/2
dc.description.none.fl_txt_mv Intrinsically photosensitive retinal ganglion cells (ipRGCs) can respond to light directly through self-contained photopigment, melanopsin. IpRGCs also receive inputs from rods and cones. Thus, studying ipRGC functions requires a novel photostimulating method that can account for all of the photoreceptor inputs. Here, we introduce an inexpensive LED-based five-primary photostimulator that can control the excitations of rods, S-, M-, L-cones and melanopsin-containing ipRGCs in humans at constant background photoreceptor excitation levels, a critical requirement for studying the adaptation behavior of ipRGCs with rod, cone or melanopsin input. We describe the theory and technical aspects (including optics, electronics, software and calibration) of the five-primary photostimulator. Then we present two preliminary studies using the photostimulator we have implemented to measure melanopsin-mediated pupil responses and temporal contrast sensitivity function (TCSF). The results showed that the S-cone input to pupil responses was antagonistic to the L-, M- or melanopsin inputs, consistent with an S-OFF and (L+M)-ON response property of primate ipRGCs (Dacey et al., 2005). In addition, the melanopsin-mediated TCSF had a distinctive pattern compared with L+M or S-cone mediated TCSF. Other than control individual photoreceptor excitation independently, the five-primary photostimulator has the flexibility in presenting stimuli modulating any combination of photoreceptor excitations, which allows to study the mechanisms by which ipRGCs combine various photoreceptor inputs.
Fil: Cao, Dingcai. University Of Illinois; Estados Unidos
Fil: Nicandro, Nathaniel. University Of Illinois; Estados Unidos
Fil: Barrionuevo, Pablo Alejandro. University Of Illinois; Estados Unidos. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina
description Intrinsically photosensitive retinal ganglion cells (ipRGCs) can respond to light directly through self-contained photopigment, melanopsin. IpRGCs also receive inputs from rods and cones. Thus, studying ipRGC functions requires a novel photostimulating method that can account for all of the photoreceptor inputs. Here, we introduce an inexpensive LED-based five-primary photostimulator that can control the excitations of rods, S-, M-, L-cones and melanopsin-containing ipRGCs in humans at constant background photoreceptor excitation levels, a critical requirement for studying the adaptation behavior of ipRGCs with rod, cone or melanopsin input. We describe the theory and technical aspects (including optics, electronics, software and calibration) of the five-primary photostimulator. Then we present two preliminary studies using the photostimulator we have implemented to measure melanopsin-mediated pupil responses and temporal contrast sensitivity function (TCSF). The results showed that the S-cone input to pupil responses was antagonistic to the L-, M- or melanopsin inputs, consistent with an S-OFF and (L+M)-ON response property of primate ipRGCs (Dacey et al., 2005). In addition, the melanopsin-mediated TCSF had a distinctive pattern compared with L+M or S-cone mediated TCSF. Other than control individual photoreceptor excitation independently, the five-primary photostimulator has the flexibility in presenting stimuli modulating any combination of photoreceptor excitations, which allows to study the mechanisms by which ipRGCs combine various photoreceptor inputs.
publishDate 2015
dc.date.none.fl_str_mv 2015-01
dc.type.none.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
http://purl.org/coar/resource_type/c_6501
info:ar-repo/semantics/articulo
format article
status_str publishedVersion
dc.identifier.none.fl_str_mv http://hdl.handle.net/11336/10617
Cao, Dingcai; Nicandro, Nathaniel; Barrionuevo, Pablo Alejandro; A five-Primary photostimulator suitable for studying intrinsically photosensitive retinal ganglion cell functions in humans; Association for Research in Vision and Ophthalmology; Journal of Vision; 15; 27; 1-2015; 1-13
1534-7362
url http://hdl.handle.net/11336/10617
identifier_str_mv Cao, Dingcai; Nicandro, Nathaniel; Barrionuevo, Pablo Alejandro; A five-Primary photostimulator suitable for studying intrinsically photosensitive retinal ganglion cell functions in humans; Association for Research in Vision and Ophthalmology; Journal of Vision; 15; 27; 1-2015; 1-13
1534-7362
dc.language.none.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv info:eu-repo/semantics/altIdentifier/url/http://jov.arvojournals.org/article.aspx?articleid=2213232
info:eu-repo/semantics/altIdentifier/doi/10.1167/15.1.27
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
eu_rights_str_mv openAccess
rights_invalid_str_mv https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
dc.format.none.fl_str_mv application/pdf
application/pdf
dc.publisher.none.fl_str_mv Association for Research in Vision and Ophthalmology
publisher.none.fl_str_mv Association for Research in Vision and Ophthalmology
dc.source.none.fl_str_mv reponame:CONICET Digital (CONICET)
instname:Consejo Nacional de Investigaciones Científicas y Técnicas
reponame_str CONICET Digital (CONICET)
collection CONICET Digital (CONICET)
instname_str Consejo Nacional de Investigaciones Científicas y Técnicas
repository.name.fl_str_mv CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicas
repository.mail.fl_str_mv dasensio@conicet.gov.ar; lcarlino@conicet.gov.ar
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score 13.006326