Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/119664
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dc.contributorSchool of Optometryen_US
dc.contributorResearch Centre for SHARP Visionen_US
dc.contributorDepartment of Industrial and Systems Engineeringen_US
dc.creatorYu, Fen_US
dc.creatorChoy, KYen_US
dc.creatorBian, Jen_US
dc.creatorShan, SSWen_US
dc.creatorTo, CHen_US
dc.creatorLi, KKen_US
dc.creatorLin, Jen_US
dc.creatorHuang, Jen_US
dc.creatorWang, Ben_US
dc.creatorTse, DYYen_US
dc.creatorChun, RKMen_US
dc.creatorLam, TCen_US
dc.date.accessioned2026-07-03T07:14:50Z-
dc.date.available2026-07-03T07:14:50Z-
dc.identifier.issn1661-6596en_US
dc.identifier.urihttp://hdl.handle.net/10397/119664-
dc.language.isoenen_US
dc.publisherMDPI AGen_US
dc.rightsCopyright: © 2026 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).en_US
dc.rightsThe following publication Yu, F., Choy, K.-Y., Bian, J., Shan, S. S.-W., To, C.-H., Li, K.-K., Lin, J., Huang, J., Wang, B., Tse, D. Y.-Y., Chun, R. K.-M., & Lam, T. C. (2026). Potential Inhibitory Effect of LED-Sourced Red Light Therapy on Ocular Growth in Normal and Myopic Chicks. International Journal of Molecular Sciences, 27(12), 5427 is available at https://doi.org/10.3390/ijms27125427.en_US
dc.subjectChicken_US
dc.subjectLEDen_US
dc.subjectLens-induced myopiaen_US
dc.subjectMyopia controlen_US
dc.subjectRed lighten_US
dc.titlePotential inhibitory effect of LED-sourced red light therapy on ocular growth in normal and myopic chicksen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.volume27en_US
dc.identifier.issue12en_US
dc.identifier.doi10.3390/ijms27125427en_US
dcterms.abstractRepeated low-level red light (RLRL) has been reported to control myopia progression clinically. Given safety concerns with laser sources, light-emitting diodes (LED)-sourced red light represents a promising alternative. This study investigated the effects of LED-sourced red light (RL) on cellular response in vitro and ocular growth in normal and lens-induced myopic chicks. In vitro, the mouse photoreceptor 661W cell line was exposed to 625 and 664 nm LED-sourced RL (3 min, twice daily) for 3 days, and cytochrome c oxidase (CCO) activity and cell viability were assessed. In vivo, chicks were randomly assigned to normal visual conditions or monocular ?5D lens-induced myopia (LIM). Treatment groups received 664 nm LED-sourced RL (30 min, twice daily) at low, moderate, or high intensities for 10 days. In vitro, LED-sourced RL at 664 nm more effectively activated CCO and enhanced cell viability in 661W cells than RL at 625 nm and white light. In vivo, low-intensity RL exposure of 10 days significantly inhibited vitreous chamber depth (VCD) and axial length (AL) elongation compared to the normal light group (p < 0.05) in normally growing chicks but showed no significant effect in LIM eyes. By contrast, moderate- and high-intensity RL exposure for 10 days attenuated myopia progression in LIM eyes, as reflected by slower VCD and AL elongation and less myopic shift, compared to the normal light group (all p < 0.05). Notably, high-intensity RL also protected the untouched fellow eyes of the LIM chick models against myopic shift and excessive elongation. LED-sourced RL at 664 nm was effective in activating CCO, reducing apoptosis, and promoting cell viability. In chick models, it can also inhibit ocular growth in both normally growing and ?5D lens-induced myopic chicks.en_US
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationInternational journal of molecular sciences, June 2026, v. 27, no. 12, 5427en_US
dcterms.isPartOfInternational journal of molecular sciencesen_US
dcterms.issued2026-06-
dc.identifier.eissn1422-0067en_US
dc.identifier.artn5427en_US
dc.description.validate202607 bcchen_US
dc.description.oaVersion of Recorden_US
dc.identifier.FolderNumbera4608-
dc.identifier.SubFormID53316-
dc.description.fundingSourceRGCen_US
dc.description.fundingSourceOthersen_US
dc.description.fundingTextThis work was supported by GRF (15104819 and 15103022), RCSV Grant (P0039545 and P0045863), RGC grant (R5032-18 and C5031-22G), UGC-ZEZ1, RMGS (P0045696), PolyU Start-up Fund for RAPs (P0044607 and P0035514), PolyU Start-up Fund for AP (P0055266), Basic Research Program of Jiangsu (BK20231222), InnoHK initiative of the Innovation and Technology Commission of the Hong Kong Special Administrative Region Government.en_US
dc.description.pubStatusPublisheden_US
dc.description.oaCategoryCCen_US
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