Cargando…

Photobiomodulation Mitigates Diabetes-Induced Retinopathy by Direct and Indirect Mechanisms: Evidence from Intervention Studies in Pigmented Mice

OBJECTIVE: Daily application of far-red light from the onset of diabetes mitigated diabetes-induced abnormalities in retinas of albino rats. Here, we test the hypothesis that photobiomodulation (PBM) is effective in diabetic, pigmented mice, even when delayed until weeks after onset of diabetes. Dir...

Descripción completa

Detalles Bibliográficos
Autores principales: Saliba, Alexandra, Du, Yunpeng, Liu, Haitao, Patel, Shyam, Roberts, Robin, Berkowitz, Bruce A., Kern, Timothy S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4591336/
https://www.ncbi.nlm.nih.gov/pubmed/26426815
http://dx.doi.org/10.1371/journal.pone.0139003
_version_ 1782393062187597824
author Saliba, Alexandra
Du, Yunpeng
Liu, Haitao
Patel, Shyam
Roberts, Robin
Berkowitz, Bruce A.
Kern, Timothy S.
author_facet Saliba, Alexandra
Du, Yunpeng
Liu, Haitao
Patel, Shyam
Roberts, Robin
Berkowitz, Bruce A.
Kern, Timothy S.
author_sort Saliba, Alexandra
collection PubMed
description OBJECTIVE: Daily application of far-red light from the onset of diabetes mitigated diabetes-induced abnormalities in retinas of albino rats. Here, we test the hypothesis that photobiomodulation (PBM) is effective in diabetic, pigmented mice, even when delayed until weeks after onset of diabetes. Direct and indirect effects of PBM on the retina also were studied. METHODS: Diabetes was induced in C57Bl/6J mice using streptozotocin. Some diabetics were exposed to PBM therapy (4 min/day; 670 nm) daily. In one study, mice were diabetic for 4 weeks before initiation of PBM for an additional 10 weeks. Retinal oxidative stress, inflammation, and retinal function were measured. In some mice, heads were covered with a lead shield during PBM to prevent direct illumination of the eye, or animals were treated with an inhibitor of heme oxygenase-1. In a second study, PBM was initiated immediately after onset of diabetes, and administered daily for 2 months. These mice were examined using manganese-enhanced MRI to assess effects of PBM on transretinal calcium channel function in vivo. RESULTS: PBM intervention improved diabetes-induced changes in superoxide generation, leukostasis, expression of ICAM-1, and visual performance. PBM acted in part remotely from the retina because the beneficial effects were achieved even with the head shielded from the light therapy, and because leukocyte-mediated cytotoxicity of retinal endothelial cells was less in diabetics treated with PBM. SnPP+PBM significantly reduced iNOS expression compared to PBM alone, but significantly exacerbated leukostasis. In study 2, PBM largely mitigated diabetes-induced retinal calcium channel dysfunction in all retinal layers. CONCLUSIONS: PBM induces retinal protection against abnormalities induced by diabetes in pigmented animals, and even as an intervention. Beneficial effects on the retina likely are mediated by both direct and indirect mechanisms. PBM is a novel non-pharmacologic treatment strategy to inhibit early changes of diabetic retinopathy.
format Online
Article
Text
id pubmed-4591336
institution National Center for Biotechnology Information
language English
publishDate 2015
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-45913362015-10-09 Photobiomodulation Mitigates Diabetes-Induced Retinopathy by Direct and Indirect Mechanisms: Evidence from Intervention Studies in Pigmented Mice Saliba, Alexandra Du, Yunpeng Liu, Haitao Patel, Shyam Roberts, Robin Berkowitz, Bruce A. Kern, Timothy S. PLoS One Research Article OBJECTIVE: Daily application of far-red light from the onset of diabetes mitigated diabetes-induced abnormalities in retinas of albino rats. Here, we test the hypothesis that photobiomodulation (PBM) is effective in diabetic, pigmented mice, even when delayed until weeks after onset of diabetes. Direct and indirect effects of PBM on the retina also were studied. METHODS: Diabetes was induced in C57Bl/6J mice using streptozotocin. Some diabetics were exposed to PBM therapy (4 min/day; 670 nm) daily. In one study, mice were diabetic for 4 weeks before initiation of PBM for an additional 10 weeks. Retinal oxidative stress, inflammation, and retinal function were measured. In some mice, heads were covered with a lead shield during PBM to prevent direct illumination of the eye, or animals were treated with an inhibitor of heme oxygenase-1. In a second study, PBM was initiated immediately after onset of diabetes, and administered daily for 2 months. These mice were examined using manganese-enhanced MRI to assess effects of PBM on transretinal calcium channel function in vivo. RESULTS: PBM intervention improved diabetes-induced changes in superoxide generation, leukostasis, expression of ICAM-1, and visual performance. PBM acted in part remotely from the retina because the beneficial effects were achieved even with the head shielded from the light therapy, and because leukocyte-mediated cytotoxicity of retinal endothelial cells was less in diabetics treated with PBM. SnPP+PBM significantly reduced iNOS expression compared to PBM alone, but significantly exacerbated leukostasis. In study 2, PBM largely mitigated diabetes-induced retinal calcium channel dysfunction in all retinal layers. CONCLUSIONS: PBM induces retinal protection against abnormalities induced by diabetes in pigmented animals, and even as an intervention. Beneficial effects on the retina likely are mediated by both direct and indirect mechanisms. PBM is a novel non-pharmacologic treatment strategy to inhibit early changes of diabetic retinopathy. Public Library of Science 2015-10-01 /pmc/articles/PMC4591336/ /pubmed/26426815 http://dx.doi.org/10.1371/journal.pone.0139003 Text en © 2015 Saliba et al http://creativecommons.org/licenses/by/4.0/ 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 properly credited.
spellingShingle Research Article
Saliba, Alexandra
Du, Yunpeng
Liu, Haitao
Patel, Shyam
Roberts, Robin
Berkowitz, Bruce A.
Kern, Timothy S.
Photobiomodulation Mitigates Diabetes-Induced Retinopathy by Direct and Indirect Mechanisms: Evidence from Intervention Studies in Pigmented Mice
title Photobiomodulation Mitigates Diabetes-Induced Retinopathy by Direct and Indirect Mechanisms: Evidence from Intervention Studies in Pigmented Mice
title_full Photobiomodulation Mitigates Diabetes-Induced Retinopathy by Direct and Indirect Mechanisms: Evidence from Intervention Studies in Pigmented Mice
title_fullStr Photobiomodulation Mitigates Diabetes-Induced Retinopathy by Direct and Indirect Mechanisms: Evidence from Intervention Studies in Pigmented Mice
title_full_unstemmed Photobiomodulation Mitigates Diabetes-Induced Retinopathy by Direct and Indirect Mechanisms: Evidence from Intervention Studies in Pigmented Mice
title_short Photobiomodulation Mitigates Diabetes-Induced Retinopathy by Direct and Indirect Mechanisms: Evidence from Intervention Studies in Pigmented Mice
title_sort photobiomodulation mitigates diabetes-induced retinopathy by direct and indirect mechanisms: evidence from intervention studies in pigmented mice
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4591336/
https://www.ncbi.nlm.nih.gov/pubmed/26426815
http://dx.doi.org/10.1371/journal.pone.0139003
work_keys_str_mv AT salibaalexandra photobiomodulationmitigatesdiabetesinducedretinopathybydirectandindirectmechanismsevidencefrominterventionstudiesinpigmentedmice
AT duyunpeng photobiomodulationmitigatesdiabetesinducedretinopathybydirectandindirectmechanismsevidencefrominterventionstudiesinpigmentedmice
AT liuhaitao photobiomodulationmitigatesdiabetesinducedretinopathybydirectandindirectmechanismsevidencefrominterventionstudiesinpigmentedmice
AT patelshyam photobiomodulationmitigatesdiabetesinducedretinopathybydirectandindirectmechanismsevidencefrominterventionstudiesinpigmentedmice
AT robertsrobin photobiomodulationmitigatesdiabetesinducedretinopathybydirectandindirectmechanismsevidencefrominterventionstudiesinpigmentedmice
AT berkowitzbrucea photobiomodulationmitigatesdiabetesinducedretinopathybydirectandindirectmechanismsevidencefrominterventionstudiesinpigmentedmice
AT kerntimothys photobiomodulationmitigatesdiabetesinducedretinopathybydirectandindirectmechanismsevidencefrominterventionstudiesinpigmentedmice