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Blue light blind-spot stimulation upregulates b-wave and pattern ERG activity in myopes

Upregulation of retinal dopaminergic activity may be a target treatment for myopia progression. This study aimed to explore the viability of inducing changes in retinal electrical activity with short-wavelength light targeting melanopsin-expressing retinal ganglion cells (ipRGCs) passing through the...

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Autores principales: Amorim-de-Sousa, Ana, Schilling, Tim, Fernandes, Paulo, Seshadri, Yeshwanth, Bahmani, Hamed, González-Méijome, José Manuel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8085027/
https://www.ncbi.nlm.nih.gov/pubmed/33927248
http://dx.doi.org/10.1038/s41598-021-88459-2
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author Amorim-de-Sousa, Ana
Schilling, Tim
Fernandes, Paulo
Seshadri, Yeshwanth
Bahmani, Hamed
González-Méijome, José Manuel
author_facet Amorim-de-Sousa, Ana
Schilling, Tim
Fernandes, Paulo
Seshadri, Yeshwanth
Bahmani, Hamed
González-Méijome, José Manuel
author_sort Amorim-de-Sousa, Ana
collection PubMed
description Upregulation of retinal dopaminergic activity may be a target treatment for myopia progression. This study aimed to explore the viability of inducing changes in retinal electrical activity with short-wavelength light targeting melanopsin-expressing retinal ganglion cells (ipRGCs) passing through the optic nerve head. Fifteen healthy non-myopic or myopic young adults were recruited and underwent stimulation with blue light using a virtual reality headset device. Amplitudes and implicit times from photopic 3.0 b-wave and pattern electroretinogram (PERG) were measured at baseline and 10 and 20 min after stimulation. Relative changes were compared between non-myopes and myopes. The ERG b-wave amplitude was significantly larger 20 min after blind-spot stimulation compared to baseline (p < 0.001) and 10 min (p < 0.001) post-stimulation. PERG amplitude P50-N95 also showed a significant main effect for ‘Time after stimulation’ (p < 0.050). Implicit times showed no differences following blind-spot stimulation. PERG and b-wave changes after blind-spot stimulation were stronger in myopes than non-myopes. It is possible to induce significant changes in retinal electrical activity by stimulating ipRGCs axons at the optic nerve head with blue light. The results suggest that the changes in retinal electrical activity are located at the inner plexiform layer and are likely to involve the dopaminergic system.
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spelling pubmed-80850272021-05-03 Blue light blind-spot stimulation upregulates b-wave and pattern ERG activity in myopes Amorim-de-Sousa, Ana Schilling, Tim Fernandes, Paulo Seshadri, Yeshwanth Bahmani, Hamed González-Méijome, José Manuel Sci Rep Article Upregulation of retinal dopaminergic activity may be a target treatment for myopia progression. This study aimed to explore the viability of inducing changes in retinal electrical activity with short-wavelength light targeting melanopsin-expressing retinal ganglion cells (ipRGCs) passing through the optic nerve head. Fifteen healthy non-myopic or myopic young adults were recruited and underwent stimulation with blue light using a virtual reality headset device. Amplitudes and implicit times from photopic 3.0 b-wave and pattern electroretinogram (PERG) were measured at baseline and 10 and 20 min after stimulation. Relative changes were compared between non-myopes and myopes. The ERG b-wave amplitude was significantly larger 20 min after blind-spot stimulation compared to baseline (p < 0.001) and 10 min (p < 0.001) post-stimulation. PERG amplitude P50-N95 also showed a significant main effect for ‘Time after stimulation’ (p < 0.050). Implicit times showed no differences following blind-spot stimulation. PERG and b-wave changes after blind-spot stimulation were stronger in myopes than non-myopes. It is possible to induce significant changes in retinal electrical activity by stimulating ipRGCs axons at the optic nerve head with blue light. The results suggest that the changes in retinal electrical activity are located at the inner plexiform layer and are likely to involve the dopaminergic system. Nature Publishing Group UK 2021-04-29 /pmc/articles/PMC8085027/ /pubmed/33927248 http://dx.doi.org/10.1038/s41598-021-88459-2 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Amorim-de-Sousa, Ana
Schilling, Tim
Fernandes, Paulo
Seshadri, Yeshwanth
Bahmani, Hamed
González-Méijome, José Manuel
Blue light blind-spot stimulation upregulates b-wave and pattern ERG activity in myopes
title Blue light blind-spot stimulation upregulates b-wave and pattern ERG activity in myopes
title_full Blue light blind-spot stimulation upregulates b-wave and pattern ERG activity in myopes
title_fullStr Blue light blind-spot stimulation upregulates b-wave and pattern ERG activity in myopes
title_full_unstemmed Blue light blind-spot stimulation upregulates b-wave and pattern ERG activity in myopes
title_short Blue light blind-spot stimulation upregulates b-wave and pattern ERG activity in myopes
title_sort blue light blind-spot stimulation upregulates b-wave and pattern erg activity in myopes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8085027/
https://www.ncbi.nlm.nih.gov/pubmed/33927248
http://dx.doi.org/10.1038/s41598-021-88459-2
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