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Injectable Phosphorescence-based Oxygen Biosensors Identify Post Ischemic Reactive Hyperoxia
Novel injectable biosensors were used to measure interstitial oxygenation before, during, and after transient ischemia. It is well known that reactive hyperemia occurs following a period of ischemia. However, increased blood flow does not necessarily mean increased oxygen tension in the tissue. Ther...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5558004/ https://www.ncbi.nlm.nih.gov/pubmed/28811566 http://dx.doi.org/10.1038/s41598-017-08490-0 |
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author | Chien, Jennifer S. Mohammed, Mahmoud Eldik, Hysem Ibrahim, Mohamed M. Martinez, Jeremy Nichols, Scott P. Wisniewski, Natalie Klitzman, Bruce |
author_facet | Chien, Jennifer S. Mohammed, Mahmoud Eldik, Hysem Ibrahim, Mohamed M. Martinez, Jeremy Nichols, Scott P. Wisniewski, Natalie Klitzman, Bruce |
author_sort | Chien, Jennifer S. |
collection | PubMed |
description | Novel injectable biosensors were used to measure interstitial oxygenation before, during, and after transient ischemia. It is well known that reactive hyperemia occurs following a period of ischemia. However, increased blood flow does not necessarily mean increased oxygen tension in the tissue. Therefore, the purpose of this study was to test the hypothesis that tissue reactive hyperoxia occurs following release of hind-limb tourniquet occlusions. Rats were injected with bilateral hind-limb biosensors and were simultaneously subjected to a unilateral femoral vessel ligation. After approximately one and three months, the rats underwent a series of oxygenation challenges, including transient hind-limb tourniquet occlusion. Along with the biosensors, near infrared spectroscopy was used to measure percent oxyhemoglobin in capillaries and laser Doppler flowmetry was used to measure blood flow. Post-occlusion reactive hyperemia was observed. It was accompanied by tissue reactive hyperoxia, affirming that the post-occlusion oxygen supply must have exceeded the expected increased oxygen consumption. The measurement of the physiologic phenomenon of reactive hyperoxia could prove clinically beneficial for both diagnosis and optimizing therapy. |
format | Online Article Text |
id | pubmed-5558004 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-55580042017-08-18 Injectable Phosphorescence-based Oxygen Biosensors Identify Post Ischemic Reactive Hyperoxia Chien, Jennifer S. Mohammed, Mahmoud Eldik, Hysem Ibrahim, Mohamed M. Martinez, Jeremy Nichols, Scott P. Wisniewski, Natalie Klitzman, Bruce Sci Rep Article Novel injectable biosensors were used to measure interstitial oxygenation before, during, and after transient ischemia. It is well known that reactive hyperemia occurs following a period of ischemia. However, increased blood flow does not necessarily mean increased oxygen tension in the tissue. Therefore, the purpose of this study was to test the hypothesis that tissue reactive hyperoxia occurs following release of hind-limb tourniquet occlusions. Rats were injected with bilateral hind-limb biosensors and were simultaneously subjected to a unilateral femoral vessel ligation. After approximately one and three months, the rats underwent a series of oxygenation challenges, including transient hind-limb tourniquet occlusion. Along with the biosensors, near infrared spectroscopy was used to measure percent oxyhemoglobin in capillaries and laser Doppler flowmetry was used to measure blood flow. Post-occlusion reactive hyperemia was observed. It was accompanied by tissue reactive hyperoxia, affirming that the post-occlusion oxygen supply must have exceeded the expected increased oxygen consumption. The measurement of the physiologic phenomenon of reactive hyperoxia could prove clinically beneficial for both diagnosis and optimizing therapy. Nature Publishing Group UK 2017-08-15 /pmc/articles/PMC5558004/ /pubmed/28811566 http://dx.doi.org/10.1038/s41598-017-08490-0 Text en © The Author(s) 2017 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 Chien, Jennifer S. Mohammed, Mahmoud Eldik, Hysem Ibrahim, Mohamed M. Martinez, Jeremy Nichols, Scott P. Wisniewski, Natalie Klitzman, Bruce Injectable Phosphorescence-based Oxygen Biosensors Identify Post Ischemic Reactive Hyperoxia |
title | Injectable Phosphorescence-based Oxygen Biosensors Identify Post Ischemic Reactive Hyperoxia |
title_full | Injectable Phosphorescence-based Oxygen Biosensors Identify Post Ischemic Reactive Hyperoxia |
title_fullStr | Injectable Phosphorescence-based Oxygen Biosensors Identify Post Ischemic Reactive Hyperoxia |
title_full_unstemmed | Injectable Phosphorescence-based Oxygen Biosensors Identify Post Ischemic Reactive Hyperoxia |
title_short | Injectable Phosphorescence-based Oxygen Biosensors Identify Post Ischemic Reactive Hyperoxia |
title_sort | injectable phosphorescence-based oxygen biosensors identify post ischemic reactive hyperoxia |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5558004/ https://www.ncbi.nlm.nih.gov/pubmed/28811566 http://dx.doi.org/10.1038/s41598-017-08490-0 |
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