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Título: Relationship between human pupillary light reflex and circadian system status
Fecha de publicación: 16-sep-2016
Editorial: Public Library of Science
Cita bibliográfica: PLoS ONE, 2016, Vol. 11, Issue 9 : e0162476
ISSN: Electronic: 1932-6203
Palabras clave: Chronobiology
Light
Sleep
Wrist
Circadian rhythms
Photoreceptors
Pupil
Circadian oscillators
Resumen: Intrinsically photosensitive retinal ganglion cells (ipRGCs), whose photopigment melanopsin has a peak of sensitivity in the short wavelength range of the spectrum, constitute a common light input pathway to the olivary pretectal nucleus (OPN), the pupillary light reflex (PLR) regulatory centre, and to the suprachiasmatic nuclei (SCN), the major pacemaker of the circadian system. Thus, evaluating PLR under short wavelength light (λmax 500 nm) and creating an integrated PLR parameter, as a possible tool to indirectly assess the status of the circadian system, becomes of interest. Nine monochromatic, photon-matched light stimuli (300 s), in 10 nm increments from λmax 420 to 500 nm were administered to 15 healthy young participants (8 females), analyzing: i) the PLR; ii) wrist temperature (WT) and motor activity rhythms (WA), iii) light exposure (L) pattern and iv) diurnal preference (HorneÖstberg), sleep quality (Pittsburgh) and daytime sleepiness (Epworth). Linear correlations between the different PLR parameters and circadian status index obtained from WT, WA and L recordings and scores from questionnaires were calculated. In summary, we found markers of robust circadian rhythms, namely high stability, reduced fragmentation, high amplitude, phase advance and low internal desynchronization, were correlated with a reduced PLR to 460–490 nm wavelengths. Integrated circadian (CSI) and PLR (cp-PLR) parameters are proposed, that also showed an inverse correlation. These results demonstrate, for the first time, the existence of a close relationship between the circadian system robustness and the pupillary reflex response, two non-visual functions primarily under melanopsin-ipRGC input.
Autor/es principal/es: Bonmati-Carrión, María Ángeles
Hild, Konstanze
Isherwood, Cheryl
Sweeney, Stephen J.
Revell, Victoria L.
Skene, Debra J.
Rol, Maria Ángeles
Madrid, Juan Antonio
Versión del editor: https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0162476
URI: http://hdl.handle.net/10201/149528
DOI: https://doi.org/10.1371/journal.pone.0162476
Tipo de documento: info:eu-repo/semantics/article
Número páginas / Extensión: 21
Derechos: info:eu-repo/semantics/openAccess
Atribución 4.0 Internacional
Descripción: © 2016 Bonmati-Carrion et al. This manuscript version is made available under the CC-BY 4.0 license http://creativecommons.org/licenses/by/4.0/ This document is the Published Manuscript version of a Published Work that appeared in final form in PLoS ONE. To access the final edited and published work see https://doi.org/10.1371/journal.pone.0162476
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