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Topical Brimonidine or Intravitreal BDNF, CNTF, or bFGF Protect Cones Against Phototoxicity

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dc.contributor.author Valiente-Soriano, Francisco-Javier
dc.contributor.author Ortin-Martínez, Arturo
dc.contributor.author Di-Pierdomenico, Johnny
dc.contributor.author García-Ayuso, Diego
dc.contributor.author Gallego-Ortega, Alejandro
dc.contributor.author Miralles-de-Imperial-Ollero, Juan-A
dc.contributor.author Jiménez-López, Manuel
dc.contributor.author Villegas-Pérez, María-Paz
dc.contributor.author Wheeler, Larry-A
dc.contributor.author Vidal-Sanz, Manuel
dc.date.accessioned 2026-02-12T11:25:57Z
dc.date.available 2026-02-12T11:25:57Z
dc.date.issued 2019-11
dc.identifier.citation Valiente-Soriano FJ, Ortín-Martínez A, Di Pierdomenico J, García-Ayuso D, Gallego-Ortega A, Miralles De Imperial-Ollero JA, et al. Topical Brimonidine or Intravitreal BDNF, CNTF, or bFGF Protect Cones Against Phototoxicity. Trans Vis Sci Tech. 17 de diciembre de 2019;8(6):36.
dc.identifier.issn 2164-2591
dc.identifier.uri https://sms.carm.es/ricsmur/handle/123456789/24112
dc.description.abstract PURPOSE: To develop a focal photoreceptor degeneration model by blue light-emitting diode (LED)-induced phototoxicity (LIP) and investigate the protective effects of topical brimonidine (BMD) or intravitreal brain-derived neurotrophic factor (BDNF), ciliary neurotrophic factor (CNTF), or basic fibroblast growth factor (bFGF). METHODS: In anesthetized, dark-adapted, adult female Swiss mice, the left eye was dilated and exposed to blue light (10 seconds, 200 lux). After LIP, full-field electroretinograms (ERG) and spectral-domain optical coherence tomography (SD-OCT) were obtained longitudinally, and reactive-Iba-1(+)monocytic cells, TUNEL(+) cells and S-opsin(+) cone outer segments were examined up to 7 days. Left eyes were treated topically with BMD (1%) or vehicle, before or right after LIP, or intravitreally with BDNF (2.5 ?g), CNTF (0.2 ?g), bFGF (0.5 ?g), or corresponding vehicle right after LIP. At 7 days, S-opsin(+) cone outer segments were counted within predetermined fixed-size areas (PFA) centered on the lesion in both flattened retinas. RESULTS: SD-OCT showed a circular region in the superior-temporal left retina with progressive thinning (207.9 ± 5.6 ?m to 160.7 ± 6.8 ?m [7 days], n = 8), increasing TUNEL(+) cells (peak at 3 days), decreasing S-opsin(+) cone outer segments, and strong microglia activation. ERGs were normal by 3 days. Total S-opsin(+) cones in the PFA for LIP-treated and fellow-retinas were 2330 ± 262 and 5601 ± 583 (n = 8), respectively. All neuroprotectants (n = 7-11), including topical BMD pre- or post-LIP, or intravitreal BDNF, CNTF, and bFGF, showed significantly greater S-opsin(+) cone survival than their corresponding vehicle-treated groups. CONCLUSIONS: LIP is a reliable, quantifiable focal photoreceptor degeneration model. Topical BMD or intravitreal BDNF, CNTF, or bFGF protect against LIP-induced cone-photoreceptor loss. TRANSLATIONAL RELEVANCE: Topical BMD or intravitreal BDNF, CNTF, or bFGF protect cones against phototoxicity.
dc.language.iso eng
dc.publisher ASSOC RESEARCH VISION OPHTHALMOLOGY INC
dc.rights Atribución/Reconocimiento-NoComercial-SinDerivados 4.0 Internaciona
dc.rights.uri http://creativecommons.org/licenses/by-nc-nd/4.0/ *
dc.title Topical Brimonidine or Intravitreal BDNF, CNTF, or bFGF Protect Cones Against Phototoxicity
dc.type info:eu-repo/semantics/article
dc.identifier.pmid 31890348
dc.relation.publisherversion https://tvst.arvojournals.org/article.aspx?articleid=2757559
dc.type.version info:eu-repo/semantics/publishedVersion
dc.identifier.doi 10.1167/tvst.8.6.36
dc.journal.title Translational Vision Science & Technology


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