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光生物调控通过多巴胺信号级联反应抑制小鼠形觉剥夺性近视进展

李俊宇 郭好运 申琪

激光生物学报2026,Vol.35Issue(2):185-192,8.
激光生物学报2026,Vol.35Issue(2):185-192,8.DOI:10.3969/j.issn.1007-7146.2026.02.010

光生物调控通过多巴胺信号级联反应抑制小鼠形觉剥夺性近视进展

Photobiomodulation Attenuates Form-Deprivation Myopia Progression in Mice through a Dopamine-Signaling Cascade

李俊宇 1郭好运 1申琪1

作者信息

  • 1. 华南师范大学光电科学与工程学院,激光生命科学研究所暨激光生命科学教育部重点实验室,广州 510631||华南师范大学光电科学与工程学院,广东省激光生命科学重点实验室,广州 510631
  • 折叠

摘要

Abstract

Photobiomodulation therapy(PBMT)has emerged as a promising non-pharmacological physical intervention for myopia control.However,the optimal irradiation parameters and the underlying mechanisms remain to be further clarified.In this study,a form-deprivation myopia(FDM)mouse model was established,and 650 nm PBMT protocols with different power densities were applied to systematically evaluate the inhibitory effect of PBMT on myopia-associated axial elongation.Changes in dopamine(DA)and nitric oxide(NO)levels in the retina were quantified,and the efficacy and safety of long-term PBMT were further assessed.In addition,ex vivo cell experiments were performed to investigate downstream molecular responses to DA.The results showed that PBMT significantly suppressed abnormal axial elongation in FDM mice(P<0.05),with the most prominent effect observed at a power density of 0.25 mW/cm2.PBMT also markedly increased DA and NO secretion in the retinal(P<0.05)in a dose-dependent manner.Long-term PBMT stably inhibited axial elongation during myopia development without significantly affecting axial length in normal mice,suggesting a favorable safety profile.Furthermore,DA upregulated cellular FBJ osteosarcoma oncogene(c-Fos)expression and promoted tissue inhibitor of metalloproteinases(TIMP2)gene expression in retinal pigment epithelial cells,and these effects were attenuated by D1R inhibition,indicating that the DA-D1R-mediated c-Fos/TIMP2 pathway may contribute to PBMT-induced suppression of axial elongation.Collectively,these findings demonstrate that PBMT effectively alleviates myopia progression in FDM mice,potentially by activating retinal DA/NO signaling and modulating molecular networks associated with tissue remodeling,thereby providing experimental evidence for parameter optimization and mechanistic exploration of red-light-based myopia interventions.

关键词

光生物调控治疗/多巴胺/近视/巩膜/视网膜色素上皮细胞

Key words

photobiomodulation therapy/dopamine/myopia/sclera/retinal pigment epithelium

分类

生物科学

引用本文复制引用

李俊宇,郭好运,申琪..光生物调控通过多巴胺信号级联反应抑制小鼠形觉剥夺性近视进展[J].激光生物学报,2026,35(2):185-192,8.

基金项目

国家自然科学基金资助项目(62305119) (62305119)

广东省自然科学基金资助项目(2023A1515011489,2025A1515011522) (2023A1515011489,2025A1515011522)

广东省科学技术协会资助项目(SKXRC2025015). (SKXRC2025015)

激光生物学报

1007-7146

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