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Retinal Oxygen Delivery, Metabolism and Extraction Fraction and Retinal Thickness Immediately Following an Interval of Ophthalmic Vessel Occlusion in Rats
Limited knowledge is currently available about alterations of retinal blood flow (F), oxygen delivery (DO(2)), oxygen metabolism (MO(2)), oxygen extraction fraction (OEF), or thickness after the ophthalmic blood vessels have been closed for a substantial interval and then reopened. We ligated the op...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6542852/ https://www.ncbi.nlm.nih.gov/pubmed/31147557 http://dx.doi.org/10.1038/s41598-019-44250-y |
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author | Blair, Norman P. Tan, Michael R. Felder, Anthony E. Shahidi, Mahnaz |
author_facet | Blair, Norman P. Tan, Michael R. Felder, Anthony E. Shahidi, Mahnaz |
author_sort | Blair, Norman P. |
collection | PubMed |
description | Limited knowledge is currently available about alterations of retinal blood flow (F), oxygen delivery (DO(2)), oxygen metabolism (MO(2)), oxygen extraction fraction (OEF), or thickness after the ophthalmic blood vessels have been closed for a substantial interval and then reopened. We ligated the ophthalmic vessels for 120 minutes in one eye of 17 rats, and measured these variables within 20 minutes after release of the ligature in the 10 rats which had immediate reflow. F, DO(2) and MO(2) were 5.2 ± 3.1 μL/min, 428 ± 271 nL O(2)/min, and 234 ± 133 nL O(2)/min, respectively, that is, to 58%, 46% and 60% of values obtained from normal fellow eyes (P < 0.004). OEF was 0.65 ± 0.23, 148% of normal (P = 0.03). Inner and total retinal thicknesses were 195 ± 24 and 293 ± 20 μm, respectively, 117% and 114% of normal, and inversely related to MO(2) (P ≤ 0.02). These results reflect how much energy is available to the retina immediately after an interval of nonperfusion for 120 minutes. Thus, they elucidate aspects of the pathophysiology of nonperfusion retinal injury and may improve therapy in patients with retinal artery or ophthalmic artery obstructions. |
format | Online Article Text |
id | pubmed-6542852 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-65428522019-06-07 Retinal Oxygen Delivery, Metabolism and Extraction Fraction and Retinal Thickness Immediately Following an Interval of Ophthalmic Vessel Occlusion in Rats Blair, Norman P. Tan, Michael R. Felder, Anthony E. Shahidi, Mahnaz Sci Rep Article Limited knowledge is currently available about alterations of retinal blood flow (F), oxygen delivery (DO(2)), oxygen metabolism (MO(2)), oxygen extraction fraction (OEF), or thickness after the ophthalmic blood vessels have been closed for a substantial interval and then reopened. We ligated the ophthalmic vessels for 120 minutes in one eye of 17 rats, and measured these variables within 20 minutes after release of the ligature in the 10 rats which had immediate reflow. F, DO(2) and MO(2) were 5.2 ± 3.1 μL/min, 428 ± 271 nL O(2)/min, and 234 ± 133 nL O(2)/min, respectively, that is, to 58%, 46% and 60% of values obtained from normal fellow eyes (P < 0.004). OEF was 0.65 ± 0.23, 148% of normal (P = 0.03). Inner and total retinal thicknesses were 195 ± 24 and 293 ± 20 μm, respectively, 117% and 114% of normal, and inversely related to MO(2) (P ≤ 0.02). These results reflect how much energy is available to the retina immediately after an interval of nonperfusion for 120 minutes. Thus, they elucidate aspects of the pathophysiology of nonperfusion retinal injury and may improve therapy in patients with retinal artery or ophthalmic artery obstructions. Nature Publishing Group UK 2019-05-30 /pmc/articles/PMC6542852/ /pubmed/31147557 http://dx.doi.org/10.1038/s41598-019-44250-y Text en © The Author(s) 2019 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Blair, Norman P. Tan, Michael R. Felder, Anthony E. Shahidi, Mahnaz Retinal Oxygen Delivery, Metabolism and Extraction Fraction and Retinal Thickness Immediately Following an Interval of Ophthalmic Vessel Occlusion in Rats |
title | Retinal Oxygen Delivery, Metabolism and Extraction Fraction and Retinal Thickness Immediately Following an Interval of Ophthalmic Vessel Occlusion in Rats |
title_full | Retinal Oxygen Delivery, Metabolism and Extraction Fraction and Retinal Thickness Immediately Following an Interval of Ophthalmic Vessel Occlusion in Rats |
title_fullStr | Retinal Oxygen Delivery, Metabolism and Extraction Fraction and Retinal Thickness Immediately Following an Interval of Ophthalmic Vessel Occlusion in Rats |
title_full_unstemmed | Retinal Oxygen Delivery, Metabolism and Extraction Fraction and Retinal Thickness Immediately Following an Interval of Ophthalmic Vessel Occlusion in Rats |
title_short | Retinal Oxygen Delivery, Metabolism and Extraction Fraction and Retinal Thickness Immediately Following an Interval of Ophthalmic Vessel Occlusion in Rats |
title_sort | retinal oxygen delivery, metabolism and extraction fraction and retinal thickness immediately following an interval of ophthalmic vessel occlusion in rats |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6542852/ https://www.ncbi.nlm.nih.gov/pubmed/31147557 http://dx.doi.org/10.1038/s41598-019-44250-y |
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