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Inner retinal oxygen metabolism in the 50/10 oxygen-induced retinopathy model
Retinopathy of prematurity (ROP) represents a major cause of childhood vision loss worldwide. The 50/10 oxygen-induced retinopathy (OIR) model mimics the findings of ROP, including peripheral vascular attenuation and neovascularization. The oxygen metabolism of the inner retina has not been previous...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4649746/ https://www.ncbi.nlm.nih.gov/pubmed/26576731 http://dx.doi.org/10.1038/srep16752 |
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author | Soetikno, Brian T. Yi, Ji Shah, Ronil Liu, Wenzhong Purta, Patryk Zhang, Hao F. Fawzi, Amani A. |
author_facet | Soetikno, Brian T. Yi, Ji Shah, Ronil Liu, Wenzhong Purta, Patryk Zhang, Hao F. Fawzi, Amani A. |
author_sort | Soetikno, Brian T. |
collection | PubMed |
description | Retinopathy of prematurity (ROP) represents a major cause of childhood vision loss worldwide. The 50/10 oxygen-induced retinopathy (OIR) model mimics the findings of ROP, including peripheral vascular attenuation and neovascularization. The oxygen metabolism of the inner retina has not been previously explored in this model. Using visible-light optical coherence tomography (vis-OCT), we measured the oxygen saturation of hemoglobin and blood flow within inner retinal vessels, enabling us to compute the inner retinal oxygen delivery (irDO(2)) and metabolic rate of oxygen (irMRO(2)). We compared these measurements between age-matched room-air controls and rats with 50/10 OIR on postnatal day 18. To account for a 61% decrease in the irDO(2) in the OIR group, we found an overall statistically significant decrease in retinal vascular density affecting the superficial and deep retinal vascular capillary networks in rats with OIR compared to controls. Furthermore, matching the reduced irDO(2), we found a 59% decrease in irMRO(2), which we correlated with a statistically significant reduction in retinal thickness in the OIR group, suggesting that the decreased irMRO(2) was due to decreased neuronal oxygen utilization. By exploring these biological and metabolic changes in great detail, our study provides an improved understanding of the pathophysiology of OIR model. |
format | Online Article Text |
id | pubmed-4649746 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-46497462015-11-23 Inner retinal oxygen metabolism in the 50/10 oxygen-induced retinopathy model Soetikno, Brian T. Yi, Ji Shah, Ronil Liu, Wenzhong Purta, Patryk Zhang, Hao F. Fawzi, Amani A. Sci Rep Article Retinopathy of prematurity (ROP) represents a major cause of childhood vision loss worldwide. The 50/10 oxygen-induced retinopathy (OIR) model mimics the findings of ROP, including peripheral vascular attenuation and neovascularization. The oxygen metabolism of the inner retina has not been previously explored in this model. Using visible-light optical coherence tomography (vis-OCT), we measured the oxygen saturation of hemoglobin and blood flow within inner retinal vessels, enabling us to compute the inner retinal oxygen delivery (irDO(2)) and metabolic rate of oxygen (irMRO(2)). We compared these measurements between age-matched room-air controls and rats with 50/10 OIR on postnatal day 18. To account for a 61% decrease in the irDO(2) in the OIR group, we found an overall statistically significant decrease in retinal vascular density affecting the superficial and deep retinal vascular capillary networks in rats with OIR compared to controls. Furthermore, matching the reduced irDO(2), we found a 59% decrease in irMRO(2), which we correlated with a statistically significant reduction in retinal thickness in the OIR group, suggesting that the decreased irMRO(2) was due to decreased neuronal oxygen utilization. By exploring these biological and metabolic changes in great detail, our study provides an improved understanding of the pathophysiology of OIR model. Nature Publishing Group 2015-11-18 /pmc/articles/PMC4649746/ /pubmed/26576731 http://dx.doi.org/10.1038/srep16752 Text en Copyright © 2015, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Soetikno, Brian T. Yi, Ji Shah, Ronil Liu, Wenzhong Purta, Patryk Zhang, Hao F. Fawzi, Amani A. Inner retinal oxygen metabolism in the 50/10 oxygen-induced retinopathy model |
title | Inner retinal oxygen metabolism in the 50/10 oxygen-induced retinopathy model |
title_full | Inner retinal oxygen metabolism in the 50/10 oxygen-induced retinopathy model |
title_fullStr | Inner retinal oxygen metabolism in the 50/10 oxygen-induced retinopathy model |
title_full_unstemmed | Inner retinal oxygen metabolism in the 50/10 oxygen-induced retinopathy model |
title_short | Inner retinal oxygen metabolism in the 50/10 oxygen-induced retinopathy model |
title_sort | inner retinal oxygen metabolism in the 50/10 oxygen-induced retinopathy model |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4649746/ https://www.ncbi.nlm.nih.gov/pubmed/26576731 http://dx.doi.org/10.1038/srep16752 |
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