Differential effects of 670 and 830 nm red near infrared irradiation therapy: a comparative study of optic nerve injury, retinal degeneration, traumatic brain and spinal cord injury

dc.contributor.authorGiacci, Marcus K.
dc.contributor.authorWheeler, Lachlan
dc.contributor.authorLovett, Sarah
dc.contributor.authorDishington, Emma
dc.contributor.authorMajda, Bernadette
dc.contributor.authorBartlett, Carole A.
dc.contributor.authorThornton, Emma
dc.contributor.authorHarford-Wright, Elizabeth
dc.contributor.authorLeonard, Anna
dc.contributor.authorVink, Robert
dc.contributor.authorHarvey, Alan R.
dc.contributor.authorProvis, Jan
dc.contributor.authorDunlop, Sarah A.
dc.contributor.authorHart, Nathan S.
dc.contributor.authorHodgetts, Stuart
dc.contributor.authorNatoli, Riccardo
dc.contributor.authorVan Den Heuvel, Corinna
dc.contributor.authorFitzgerald, Melinda
dc.date.accessioned2015-10-21T23:26:04Z
dc.date.available2015-10-21T23:26:04Z
dc.date.issued2014-08-08
dc.date.updated2015-12-08T10:30:01Z
dc.description.abstractRed/near-infrared irradiation therapy (R/NIR-IT) delivered by laser or light-emitting diode (LED) has improved functional outcomes in a range of CNS injuries. However, translation of R/NIR-IT to the clinic for treatment of neurotrauma has been hampered by lack of comparative information regarding the degree of penetration of the delivered irradiation to the injury site and the optimal treatment parameters for different CNS injuries. We compared the treatment efficacy of R/NIR-IT at 670 nm and 830 nm, provided by narrow-band LED arrays adjusted to produce equal irradiance, in four in vivo rat models of CNS injury: partial optic nerve transection, light-induced retinal degeneration, traumatic brain injury (TBI) and spinal cord injury (SCI). The number of photons of 670 nm or 830 nm light reaching the SCI injury site was 6.6% and 11.3% of emitted light respectively. Treatment of rats with 670 nm R/NIR-IT following partial optic nerve transection significantly increased the number of visual responses at 7 days after injury (P ≤ 0.05); 830 nm R/NIR-IT was partially effective. 670 nm R/NIR-IT also significantly reduced reactive species and both 670 nm and 830 nm R/NIR-IT reduced hydroxynonenal immunoreactivity (P ≤ 0.05) in this model. Pre-treatment of light-induced retinal degeneration with 670 nm R/NIR-IT significantly reduced the number of Tunel+ cells and 8-hydroxyguanosine immunoreactivity (P ≤ 0.05); outcomes in 830 nm R/NIR-IT treated animals were not significantly different to controls. Treatment of fluid-percussion TBI with 670 nm or 830 nm R/NIR-IT did not result in improvements in motor or sensory function or lesion size at 7 days (P>0.05). Similarly, treatment of contusive SCI with 670 nm or 830 nm R/NIR-IT did not result in significant improvements in functional recovery or reduced cyst size at 28 days (P>0.05). Outcomes from this comparative study indicate that it will be necessary to optimise delivery devices, wavelength, intensity and duration of R/NIR-IT individually for different CNS injury types.
dc.description.sponsorshipThis work was supported by the Neurotrauma Research Program (Western Australia) (http://www.nrp.org.au/). This project is funded through the Road Trauma Trust Account, but does not reflect views or recommendations of the Road Safety Council. NSH was funded by The University of Western Australia and The Western Australian State Government as part of a Western Australian Premiers Fellowship to Prof. Shaun Collin.en_AU
dc.format15 pages
dc.identifier.issn1932-6203en_AU
dc.identifier.urihttp://hdl.handle.net/1885/16017
dc.publisherPublic Library of Science
dc.rights© 2014 Giacci 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.subjectred/near-infrared irradiation therapy (R/NIR-IT)
dc.subjectlight-emitting diode (LED)
dc.subjectcentral nervous system (CNS) injury
dc.subjecttreatment
dc.subjectneurotrauma
dc.subjectcomparative information
dc.subjectoptimal treatment parameters
dc.subjectdegree of penetration
dc.subjectirradiation
dc.subjectinjury site
dc.subject670 nm and 830 nm
dc.subjectvivo rat models
dc.titleDifferential effects of 670 and 830 nm red near infrared irradiation therapy: a comparative study of optic nerve injury, retinal degeneration, traumatic brain and spinal cord injury
dc.typeJournal article
dcterms.dateAccepted2014-07-10
local.bibliographicCitation.issue8en_AU
local.bibliographicCitation.lastpage15
local.bibliographicCitation.startpagee104565en_AU
local.contributor.affiliationGiacci, Markus K, The University of Western Australia, Australiaen_AU
local.contributor.affiliationWheeler, Lachlan, The University of Western Australia, Australiaen_AU
local.contributor.affiliationLovett, Sarah, The University of Western Australia, Australiaen_AU
local.contributor.affiliationDishington, Emma, The University of Western Australia, Australiaen_AU
local.contributor.affiliationMajda, Bernadette, University of Western Australia, Australiaen_AU
local.contributor.affiliationBartlett, Carole A, The University of Western Australia, Australiaen_AU
local.contributor.affiliationThornton, Emma, The University of Adelaide,, Australiaen_AU
local.contributor.affiliationHarford-Wright, Elizabeth, The University of Adelaide , Australiaen_AU
local.contributor.affiliationLeonard, Anna, The University of Adelaide, Australiaen_AU
local.contributor.affiliationVink, Robert, The University of Adelaide, Australiaen_AU
local.contributor.affiliationHarvey, A.R., University of Western Australia, Australiaen_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.affiliationDunlop, Sarah Alison, University of Western Australia, Australiaen_AU
local.contributor.affiliationHart, Nathan, University of Western Australia, Australiaen_AU
local.contributor.affiliationHodgetts, Stuart, The University of Western Australia, Australiaen_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.affiliationVan Den Heuvel, Corinna, The University of Adelaide, Australiaen_AU
local.contributor.affiliationFitzgerald, Melinda, The University of Western Australia, Australiaen_AU
local.contributor.authoruidu4118802en_AU
local.description.notesImported from ARIESen_AU
local.identifier.absfor111301en_AU
local.identifier.absfor110903en_AU
local.identifier.ariespublicationu4693331xPUB140en_AU
local.identifier.citationvolume9en_AU
local.identifier.doi10.1371/journal.pone.0104565en_AU
local.identifier.essn1932-6203en_AU
local.identifier.scopusID2-s2.0-84905640324
local.identifier.thomsonID000343231900072
local.publisher.urlhttps://www.plos.org/en_AU
local.type.statusPublished Versionen_AU

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