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670nm Photobiomodulation as a Novel Protection against Retinopathy of Prematurity: Evidence from Oxygen Induced Retinopathy Models

dc.contributor.authorNatoli, Riccardo
dc.contributor.authorValter, Krisztina
dc.contributor.authorBarbosa, Marconi
dc.contributor.authorDahlstrom, Jane
dc.contributor.authorRutar, Matthew
dc.contributor.authorKent, Alison
dc.contributor.authorProvis, Jan
dc.date.accessioned2015-11-24T04:40:16Z
dc.date.available2015-11-24T04:40:16Z
dc.date.issued2013-08-08
dc.date.updated2015-12-11T08:24:55Z
dc.description.abstractINTRODUCTION To investigate the validity of using 670nm red light as a preventative treatment for Retinopathy of Prematurity in two animal models of oxygen-induced retinopathy (OIR). MATERIALS AND METHODS During and post exposure to hyperoxia, C57BL/6J mice or Sprague-Dawley rats were exposed to 670 nm light for 3 minutes a day (9J/cm²). Whole mounted retinas were investigated for evidence of vascular abnormalities, while sections of neural retina were used to quantify levels of cell death using the TUNEL technique. Organs were removed, weighed and independent histopathology examination performed. RESULTS 670 nm light reduced neovascularisation, vaso-obliteration and abnormal peripheral branching patterns of retinal vessels in OIR. The neural retina was also protected against OIR by 670 nm light exposure. OIR-exposed animals had severe lung pathology, including haemorrhage and oedema, that was significantly reduced in 670 nm+OIR light-exposed animals. There were no significance differences in the organ weights of animals in the 670 nm light-exposed animals, and no adverse effects of exposure to 670 nm light were detected. DISCUSSION Low levels of exposure to 670 nm light protects against OIR and lung damage associated with exposure to high levels of oxygen, and may prove to be a non-invasive and inexpensive preventative treatment for ROP and chronic lung disease associated with prematurity.
dc.description.sponsorshipAustralian Research Council Centres of Excellence Program Grant (CE0561903); Canberra Hospital Private Practice Fund. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.en_AU
dc.identifier.issn1932-6203en_AU
dc.identifier.urihttp://hdl.handle.net/1885/16651
dc.publisherPublic Library of Science
dc.relationhttp://purl.org/au-research/grants/arc/CE0561903
dc.rights© 2013 Natoli et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
dc.sourcePLoS ONE
dc.subjectanimals
dc.subjectlung
dc.subjectlung diseases
dc.subjectmice
dc.subjectmice, inbred c57bl
dc.subjectneovascularization, pathologic
dc.subjectoxygen
dc.subjectphototherapy
dc.subjectrats
dc.subjectrats, sprague-dawley
dc.subjectretina
dc.subjectretinal vessels
dc.subjectretinopathy of prematurity
dc.title670nm Photobiomodulation as a Novel Protection against Retinopathy of Prematurity: Evidence from Oxygen Induced Retinopathy Models
dc.typeJournal article
local.bibliographicCitation.issue8en_AU
local.bibliographicCitation.startpagee72135en_AU
local.contributor.affiliationNatoli, Riccardo, College of Medicine, Biology and Environment, CMBE John Curtin School of Medical Research, Eccles Institute of Neuroscience, The Australian National Universityen_AU
local.contributor.affiliationValter (Valter-Kocsi), Krisztina, College of Medicine, Biology and Environment, CMBE John Curtin School of Medical Research, Eccles Institute of Neuroscience, The Australian National Universityen_AU
local.contributor.affiliationBarbosa, Marconi, College of Medicine, Biology and Environment, CMBE Research School of Biology, Division of Biomedical Science and Biochemistry, The Australian National Universityen_AU
local.contributor.affiliationDahlstrom, Jane, College of Medicine, Biology and Environment, CMBE ANU Medical School, ANU Medical School, The Australian National Universityen_AU
local.contributor.affiliationRutar, Matthew, College of Medicine, Biology and Environment, CMBE John Curtin School of Medical Research, Eccles Institute of Neuroscience, The Australian National Universityen_AU
local.contributor.affiliationKent, Alison, College of Medicine, Biology and Environment, CMBE ANU Medical School, ANU Medical School, The Australian National Universityen_AU
local.contributor.affiliationProvis, Jan, College of Medicine, Biology and Environment, CMBE John Curtin School of Medical Research, Eccles Institute of Neuroscience, The Australian National Universityen_AU
local.contributor.authoruidNatoli, Riccardo, u4100537en_AU
local.description.notesImported from ARIESen_AU
local.identifier.absfor060399en_AU
local.identifier.absfor110316en_AU
local.identifier.absfor110900en_AU
local.identifier.ariespublicationf5625xPUB3790en_AU
local.identifier.citationvolume8en_AU
local.identifier.doi10.1371/journal.pone.0072135en_AU
local.identifier.essn1932-6203en_AU
local.identifier.scopusID2-s2.0-84881341951
local.identifier.thomsonID000323124000079
local.type.statusPublished Versionen_AU

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