Effects of circadian rhythm disruption on retinal physiopathology: Considerations from a consensus of experts.


Journal

European journal of ophthalmology
ISSN: 1724-6016
Titre abrégé: Eur J Ophthalmol
Pays: United States
ID NLM: 9110772

Informations de publication

Date de publication:
Sep 2022
Historique:
pubmed: 4 6 2022
medline: 13 8 2022
entrez: 3 6 2022
Statut: ppublish

Résumé

The circadian rhythms originate within the organism and synchronize with cyclic fluctuations in the external environment. It has been demonstrated that part of the human genome is under control of the circadian clock and that a synchronizer that helps to maintain daily rhythms is Melatonin, a neuro-hormone primarily synthesized by the pineal gland during the night. The chronic disruption of circadian rhythm has been linked to many conditions such as obesity, metabolic syndrome, type 2 diabetes, cancer, and neurodegenerative diseases. Studies in the mice showed that the disruption of the retinal circadian rhythm increases the decline during the aging of photoreceptors, accelerating age-related disruption of cone cell structure, function, and viability and that the melatonin receptor deletion seems to influence the health of retinal cells, speeding up their aging. In conclusion, preserving the circadian rhythms could be to add to the prevention and treatment of age-related degenerative retinal diseases, and although additional studies are needed, melatonin could be a valid support to favor this "chronoprotection action".

Identifiants

pubmed: 35656746
doi: 10.1177/11206721221106149
pmc: PMC9373193
doi:

Substances chimiques

Melatonin JL5DK93RCL

Types de publication

Editorial

Langues

eng

Sous-ensembles de citation

IM

Pagination

2489-2493

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Auteurs

M Parravano (M)

61870IRCCS-Fondazione Bietti, Rome, Italy.

C M Eandi (CM)

Department of Surgical Sciences, University of Torino, Torino, Italy.
Fondation Asile des Aveugles, Jules Gonin Eye Hospital, University of Lausanne, Lausanne, Switzerland.
Macula Onlus Foundation, Genoa, Italy.

M Figus (M)

Department of Surgical, Medical and Molecular Pathology and Critical Care Medicine, 9310University of Pisa, Pisa, Italy.

M Lupidi (M)

Macula Onlus Foundation, Genoa, Italy.
Eye Clinic, Department of Experimental and Clinical Medicine, Marche Polytechnic University, Ancona, Italy.

F Menchini (F)

Department of Medicine-Ophthalmology, University of Udine, Udine, Italy.

M Nicolo (M)

Macula Onlus Foundation, Genoa, Italy.
Department of Neurosciences, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health (DiNOGMI), 9302University of Genoa, Genoa, Italy.
IRCCS Ospedale Policlinico San Martino, University Eye Clinic of Genoa, Genoa, Italy.

V Parisi (V)

61870IRCCS-Fondazione Bietti, Rome, Italy.

L Toto (L)

Ophthalmic Clinic, Department of Medicine and Science of Ageing, University "G. 9301d'Annunzio" of Chieti-Pescara, Chieti, Italy.

F Viola (F)

Foundation IRCCS Cà Grande Ospedale Maggiore Policlinico, 9304University of Milan, Milan, Italy.

S Vujosevic (S)

Department of Biomedical, Surgical and Dental Sciences University of Milan, Milan, Italy.
Eye Clinic, IRCCS MultiMedica, Milan, Italy.

G Querques (G)

Department of Ophthalmology, IRCCS Ospedale San Raffaele, University Vita-Salute, Milan, Italy.

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Classifications MeSH