Comparative Neurology of Circadian Photoreception: The Retinohypothalamic Tract (RHT) in Sighted and Naturally Blind Mammals

Publikation: Bidrag til tidsskriftReviewForskningfagfællebedømt

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Comparative Neurology of Circadian Photoreception : The Retinohypothalamic Tract (RHT) in Sighted and Naturally Blind Mammals. / Hannibal, Jens.

I: Frontiers in Neuroscience, Bind 15, 640113, 2021.

Publikation: Bidrag til tidsskriftReviewForskningfagfællebedømt

Harvard

Hannibal, J 2021, 'Comparative Neurology of Circadian Photoreception: The Retinohypothalamic Tract (RHT) in Sighted and Naturally Blind Mammals', Frontiers in Neuroscience, bind 15, 640113. https://doi.org/10.3389/fnins.2021.640113

APA

Hannibal, J. (2021). Comparative Neurology of Circadian Photoreception: The Retinohypothalamic Tract (RHT) in Sighted and Naturally Blind Mammals. Frontiers in Neuroscience, 15, [640113]. https://doi.org/10.3389/fnins.2021.640113

Vancouver

Hannibal J. Comparative Neurology of Circadian Photoreception: The Retinohypothalamic Tract (RHT) in Sighted and Naturally Blind Mammals. Frontiers in Neuroscience. 2021;15. 640113. https://doi.org/10.3389/fnins.2021.640113

Author

Hannibal, Jens. / Comparative Neurology of Circadian Photoreception : The Retinohypothalamic Tract (RHT) in Sighted and Naturally Blind Mammals. I: Frontiers in Neuroscience. 2021 ; Bind 15.

Bibtex

@article{89441300f449415b87956003575d8acd,
title = "Comparative Neurology of Circadian Photoreception: The Retinohypothalamic Tract (RHT) in Sighted and Naturally Blind Mammals",
abstract = "The mammalian eye contains two systems for light perception: an image detecting system constituted primarily of the classical photoreceptors, rods and cones, and a non-image forming system (NIF) constituted of a small group of intrinsically photosensitive retinal ganglion cells driven by melanopsin (mRGCs). The mRGCs receive input from the outer retina and NIF mediates light entrainment of circadian rhythms, masking behavior, light induced inhibition of nocturnal melatonin secretion, pupillary reflex (PLR), and affect the sleep/wake cycle. This review focuses on the mammalian NIF and its anatomy in the eye as well as its neuronal projection to the brain. This pathway is known as the retinohypothalamic tract (RHT). The development and functions of the NIF as well as the knowledge gained from studying gene modified mice is highlighted. Furthermore, the similarities of the NIF between sighted (nocturnal and diurnal rodent species, monkeys, humans) and naturally blind mammals (blind mole rats Spalax ehrenbergi and the Iberian mole, Talpa occidentalis) are discussed in relation to a changing world where increasing exposure to artificial light at night (ALAN) is becoming a challenge for humans and animals in the modern society.",
keywords = "circadian rhythms, entrainment, neurotransmitters, photoreceptors, pupil reflex",
author = "Jens Hannibal",
note = "Publisher Copyright: {\textcopyright} Copyright {\textcopyright} 2021 Hannibal.",
year = "2021",
doi = "10.3389/fnins.2021.640113",
language = "English",
volume = "15",
journal = "Frontiers in Neuroscience",
issn = "1662-4548",
publisher = "Frontiers Research Foundation",

}

RIS

TY - JOUR

T1 - Comparative Neurology of Circadian Photoreception

T2 - The Retinohypothalamic Tract (RHT) in Sighted and Naturally Blind Mammals

AU - Hannibal, Jens

N1 - Publisher Copyright: © Copyright © 2021 Hannibal.

PY - 2021

Y1 - 2021

N2 - The mammalian eye contains two systems for light perception: an image detecting system constituted primarily of the classical photoreceptors, rods and cones, and a non-image forming system (NIF) constituted of a small group of intrinsically photosensitive retinal ganglion cells driven by melanopsin (mRGCs). The mRGCs receive input from the outer retina and NIF mediates light entrainment of circadian rhythms, masking behavior, light induced inhibition of nocturnal melatonin secretion, pupillary reflex (PLR), and affect the sleep/wake cycle. This review focuses on the mammalian NIF and its anatomy in the eye as well as its neuronal projection to the brain. This pathway is known as the retinohypothalamic tract (RHT). The development and functions of the NIF as well as the knowledge gained from studying gene modified mice is highlighted. Furthermore, the similarities of the NIF between sighted (nocturnal and diurnal rodent species, monkeys, humans) and naturally blind mammals (blind mole rats Spalax ehrenbergi and the Iberian mole, Talpa occidentalis) are discussed in relation to a changing world where increasing exposure to artificial light at night (ALAN) is becoming a challenge for humans and animals in the modern society.

AB - The mammalian eye contains two systems for light perception: an image detecting system constituted primarily of the classical photoreceptors, rods and cones, and a non-image forming system (NIF) constituted of a small group of intrinsically photosensitive retinal ganglion cells driven by melanopsin (mRGCs). The mRGCs receive input from the outer retina and NIF mediates light entrainment of circadian rhythms, masking behavior, light induced inhibition of nocturnal melatonin secretion, pupillary reflex (PLR), and affect the sleep/wake cycle. This review focuses on the mammalian NIF and its anatomy in the eye as well as its neuronal projection to the brain. This pathway is known as the retinohypothalamic tract (RHT). The development and functions of the NIF as well as the knowledge gained from studying gene modified mice is highlighted. Furthermore, the similarities of the NIF between sighted (nocturnal and diurnal rodent species, monkeys, humans) and naturally blind mammals (blind mole rats Spalax ehrenbergi and the Iberian mole, Talpa occidentalis) are discussed in relation to a changing world where increasing exposure to artificial light at night (ALAN) is becoming a challenge for humans and animals in the modern society.

KW - circadian rhythms

KW - entrainment

KW - neurotransmitters

KW - photoreceptors

KW - pupil reflex

U2 - 10.3389/fnins.2021.640113

DO - 10.3389/fnins.2021.640113

M3 - Review

C2 - 34054403

AN - SCOPUS:85107034640

VL - 15

JO - Frontiers in Neuroscience

JF - Frontiers in Neuroscience

SN - 1662-4548

M1 - 640113

ER -

ID: 302058581