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      Review on age-related differences in non-visual effects of light: melatonin suppression, circadian phase shift and pupillary light reflex in children to older adults

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          Abstract

          Physiological effects of light exposure in humans are diverse. Among them, the circadian rhythm phase shift effect in order to maintain a 24-h cycle of the biological clock is referred to as non-visual effects of light collectively with melatonin suppression and pupillary light reflex. The non-visual effects of light may differ depending on age, and clarifying age-related differences in the non-visual effects of light is important for providing appropriate light environments for people of different ages. Therefore, in various research fields, including physiological anthropology, many studies on the effects of age on non-visual functions have been carried out in older people, children and adolescents by comparing the effects with young adults. However, whether the non-visual effects of light vary depending on age and, if so, what factors contribute to the differences have remained unclear. In this review, results of past and recent studies on age-related differences in the non-visual effects of light are presented and discussed in order to provide clues for answering the question of whether non-visual effects of light actually vary depending on age. Some studies, especially studies focusing on older people, have shown age-related differences in non-visual functions including differences in melatonin suppression, circadian phase shift and pupillary light reflex, while other studies have shown no differences. Studies showing age-related differences in the non-visual effects of light have suspected senile constriction and crystalline lens opacity as factors contributing to the differences, while studies showing no age-related differences have suspected the presence of a compensatory mechanism. Some studies in children and adolescents have shown that children’s non-visual functions may be highly sensitive to light, but the studies comparing with other age groups seem to have been limited. In order to study age-related differences in non-visual effects in detail, comparative studies should be conducted using subjects having a wide range of ages and with as much control as possible for intensity, wavelength component, duration, circadian timing, illumination method of light exposure, and other factors (mydriasis or non-mydriasis, cataracts or not in the older adults, etc.).

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          Most cited references115

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          Phototransduction by retinal ganglion cells that set the circadian clock.

          Light synchronizes mammalian circadian rhythms with environmental time by modulating retinal input to the circadian pacemaker-the suprachiasmatic nucleus (SCN) of the hypothalamus. Such photic entrainment requires neither rods nor cones, the only known retinal photoreceptors. Here, we show that retinal ganglion cells innervating the SCN are intrinsically photosensitive. Unlike other ganglion cells, they depolarized in response to light even when all synaptic input from rods and cones was blocked. The sensitivity, spectral tuning, and slow kinetics of this light response matched those of the photic entrainment mechanism, suggesting that these ganglion cells may be the primary photoreceptors for this system.
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            Loss of a circadian adrenal corticosterone rhythm following suprachiasmatic lesions in the rat.

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              Melanopsin-containing retinal ganglion cells: architecture, projections, and intrinsic photosensitivity.

              The primary circadian pacemaker, in the suprachiasmatic nucleus (SCN) of the mammalian brain, is photoentrained by light signals from the eyes through the retinohypothalamic tract. Retinal rod and cone cells are not required for photoentrainment. Recent evidence suggests that the entraining photoreceptors are retinal ganglion cells (RGCs) that project to the SCN. The visual pigment for this photoreceptor may be melanopsin, an opsin-like protein whose coding messenger RNA is found in a subset of mammalian RGCs. By cloning rat melanopsin and generating specific antibodies, we show that melanopsin is present in cell bodies, dendrites, and proximal axonal segments of a subset of rat RGCs. In mice heterozygous for tau-lacZ targeted to the melanopsin gene locus, beta-galactosidase-positive RGC axons projected to the SCN and other brain nuclei involved in circadian photoentrainment or the pupillary light reflex. Rat RGCs that exhibited intrinsic photosensitivity invariably expressed melanopsin. Hence, melanopsin is most likely the visual pigment of phototransducing RGCs that set the circadian clock and initiate other non-image-forming visual functions.
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                Author and article information

                Contributors
                higu-s@design.kyushu-u.ac.jp
                Journal
                J Physiol Anthropol
                J Physiol Anthropol
                Journal of Physiological Anthropology
                BioMed Central (London )
                1880-6791
                1880-6805
                24 June 2023
                24 June 2023
                2023
                : 42
                : 11
                Affiliations
                [1 ]GRID grid.54432.34, ISNI 0000 0001 0860 6072, Research Fellow of the Japan Society for the Promotion of Science, ; Kodaira, Japan
                [2 ]GRID grid.416859.7, ISNI 0000 0000 9832 2227, Department of Sleep-Wake Disorders, National Center of Neurology and Psychiatry, , National Institute of Mental Health, ; Kodaira, Japan
                [3 ]GRID grid.177174.3, ISNI 0000 0001 2242 4849, Department of Human Life Design and Science, Faculty of Design, , Kyushu University, ; Fukuoka, Japan
                Author information
                http://orcid.org/0000-0002-0347-7408
                http://orcid.org/0000-0001-7131-0792
                Article
                328
                10.1186/s40101-023-00328-1
                10290329
                37355647
                d53bc0bf-8613-49a3-847b-e5e369ce0ffc
                © The Author(s) 2023

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

                History
                : 6 January 2023
                : 15 June 2023
                Funding
                Funded by: JSPS KAKENHI
                Award ID: JP23H02569
                Award ID: JP23K14278
                Award ID: JP20H01659
                Award Recipient :
                Categories
                Review
                Custom metadata
                © The Japan Society of Physiological Anthropology 2023

                Anthropology
                aging,non-image forming effect,older adults,children,light,crystalline lens,pupil,melatonin,circadian rhythm,pupillary light reflex

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