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dc.contributor.authorThomas, Chloe N
dc.contributor.authorCourtie, Ella
dc.contributor.authorBernardo-Colón, Alexandra
dc.contributor.authorEssex, Gareth
dc.contributor.authorRex, Tonia S
dc.contributor.authorAhmed, Zubair
dc.contributor.authorBlanch, Richard J
dc.date.accessioned2024-11-21T15:27:30Z
dc.date.available2024-11-21T15:27:30Z
dc.date.issued2020-06-06
dc.identifier.citationThomas CN, Courtie E, Bernardo-Colón A, Essex G, Rex TS, Ahmed Z, Blanch RJ. Assessment of necroptosis in the retina in a repeated primary ocular blast injury mouse model. Exp Eye Res. 2020 Aug;197:108102. doi: 10.1016/j.exer.2020.108102. Epub 2020 Jun 6en_US
dc.identifier.issn0014-4835
dc.identifier.eissn1096-0007
dc.identifier.doi10.1016/j.exer.2020.108102
dc.identifier.pmid32522477
dc.identifier.urihttp://hdl.handle.net/20.500.14200/6575
dc.description.abstractPrimary blast injury (caused by the initial rapid increase in pressure following an explosive blast) to the retina and optic nerve (ON) causes progressive visual loss and neurodegeneration. Military personnel are exposed to multiple low-overpressure blast waves, which may be in quick succession, such as during breacher training or in combat. We investigated the necroptotic cell death pathway in the retina in a mouse repeated primary ocular blast injury (rPBI) model using immunohistochemistry. We further evaluated whether intravitreal injections of a potent necroptosis inhibitor, Necrostatin-1s (Nec-1s), protects the retina and ON axons by retinal ganglion cells (RGC) counts, ON axonal counting and optical coherence tomography (OCT) analysis of vitreous haze. Receptor interacting protein kinase (RIPK) 3, increased in the inner plexiform layer 2 days post injury (dpi) and persisted until 14 dpi, whilst RIPK1 protein expression did not change after injury. The number of degenerating ON axons was increased at 28 dpi but there was no evidence of a reduction in the number of intact ON axons or RNA-binding protein with multiple splicing (RBPMS)+ RGC in the retina by 28 dpi in animals not receiving any intravitreal injections. But, when intravitreal injections (vehicle or Nec-1s) were given there was a significant reduction in RBPMS+ RGC numbers, suggesting that rPBI with intraocular injections is damaging to RGC. There were fewer RGC lost after Nec-1s than vehicle injection, but there was no effect of Nec-1s or vehicle treatment on the number of degenerating axons. OCT analysis demonstrated no effect of rPBI on vitreous haze, but intravitreal injection combined with rPBI increased vitreous haze (P = 0.004). Whilst necroptosis may be an active cell death signalling pathway after rPBI, its inhibition did not prevent cell death, and intravitreal injections in combination with rPBI increased vitreous inflammation and reduced RBPMS+en_US
dc.language.isoenen_US
dc.publisherAcademic Pressen_US
dc.relation.urlhttps://www.sciencedirect.com/journal/experimental-eye-researchen_US
dc.rightsCopyright © 2020 Elsevier Ltd. All rights reserved.
dc.subjectNeurologyen_US
dc.titleAssessment of necroptosis in the retina in a repeated primary ocular blast injury mouse model.en_US
dc.typeArticleen_US
dc.source.journaltitleExperimental Eye Researchen_US
dc.source.volume197
dc.source.beginpage108102
dc.source.endpage
dc.source.countryUnited States
dc.source.countryUnited States
dc.source.countryUnited States
dc.source.countryUnited States
dc.source.countryUnited States
dc.source.countryEngland
rioxxterms.versionNAen_US
dc.contributor.trustauthorBlanch, Richard J
dc.contributor.departmentOphthalmologyen_US
dc.contributor.roleMedical and Dentalen_US
oa.grant.openaccessnaen_US


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