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Timeline of Multi-Organ Plasma Extravasation After Bleomycin-Induced Acute Lung Injury
Acute lung injury (ALI) is characterized by the abrupt onset of clinically significant hypoxemia in the context of non-hydrostatic pulmonary edema. Acute lung injury is associated with cytokine release and plasma extravasation (PEx) that can cause pulmonary edema and subsequently acute respiratory d...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8841715/ https://www.ncbi.nlm.nih.gov/pubmed/35173628 http://dx.doi.org/10.3389/fphys.2022.777072 |
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author | Kitzerow, Oliver Zucker, Irving H. Lisco, Steven J. Wang, Han-Jun |
author_facet | Kitzerow, Oliver Zucker, Irving H. Lisco, Steven J. Wang, Han-Jun |
author_sort | Kitzerow, Oliver |
collection | PubMed |
description | Acute lung injury (ALI) is characterized by the abrupt onset of clinically significant hypoxemia in the context of non-hydrostatic pulmonary edema. Acute lung injury is associated with cytokine release and plasma extravasation (PEx) that can cause pulmonary edema and subsequently acute respiratory distress syndrome (ARDS). Therefore, it is critical we understand the relationship between ALI and lung PEx. In addition, it is also important to assess PEx in the lungs and other organs post-ALI since ALI/ARDS often causes multi-organ failure. We hypothesized that ALI induces time-dependent lung PEx, which promotes extravasation in the heart, liver, kidney, spleen, pancreas, and gastrointestinal (GI) tract, in a time-dependent manner. To test our hypothesis, we administered bleomycin or saline via tracheal intubation in 8-week-old Sprague Dawley rats. At the terminal experiments, Evans Blue was injected (IV) through the femoral vein to allow for the visualization of PEx. Plasma extravasation of desired organs was evaluated at 3-, 7-, 14-, 21-, and 28-days after bleomycin or saline treatment by evaluating Evans Blue concentrations calorimetrically at fluorescence excitation wavelength of 620 nm (bandwidth 10 nm) and an emission wavelength of 680 nm (bandwidth 40 nm). Data show that ALI induces lung PEx beginning at day 3 and peaking between 7 and 21 days. Extravasation was also seen in all organs at varying degrees beginning at day 3 and peaking between days 7 and 14. Resolution appears to start after day 21 and continues past day 28. We conclude that ALI caused by bleomycin incites a time-dependent PEx of the lungs and multiple other organs. |
format | Online Article Text |
id | pubmed-8841715 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-88417152022-02-15 Timeline of Multi-Organ Plasma Extravasation After Bleomycin-Induced Acute Lung Injury Kitzerow, Oliver Zucker, Irving H. Lisco, Steven J. Wang, Han-Jun Front Physiol Physiology Acute lung injury (ALI) is characterized by the abrupt onset of clinically significant hypoxemia in the context of non-hydrostatic pulmonary edema. Acute lung injury is associated with cytokine release and plasma extravasation (PEx) that can cause pulmonary edema and subsequently acute respiratory distress syndrome (ARDS). Therefore, it is critical we understand the relationship between ALI and lung PEx. In addition, it is also important to assess PEx in the lungs and other organs post-ALI since ALI/ARDS often causes multi-organ failure. We hypothesized that ALI induces time-dependent lung PEx, which promotes extravasation in the heart, liver, kidney, spleen, pancreas, and gastrointestinal (GI) tract, in a time-dependent manner. To test our hypothesis, we administered bleomycin or saline via tracheal intubation in 8-week-old Sprague Dawley rats. At the terminal experiments, Evans Blue was injected (IV) through the femoral vein to allow for the visualization of PEx. Plasma extravasation of desired organs was evaluated at 3-, 7-, 14-, 21-, and 28-days after bleomycin or saline treatment by evaluating Evans Blue concentrations calorimetrically at fluorescence excitation wavelength of 620 nm (bandwidth 10 nm) and an emission wavelength of 680 nm (bandwidth 40 nm). Data show that ALI induces lung PEx beginning at day 3 and peaking between 7 and 21 days. Extravasation was also seen in all organs at varying degrees beginning at day 3 and peaking between days 7 and 14. Resolution appears to start after day 21 and continues past day 28. We conclude that ALI caused by bleomycin incites a time-dependent PEx of the lungs and multiple other organs. Frontiers Media S.A. 2022-01-31 /pmc/articles/PMC8841715/ /pubmed/35173628 http://dx.doi.org/10.3389/fphys.2022.777072 Text en Copyright © 2022 Kitzerow, Zucker, Lisco and Wang. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Physiology Kitzerow, Oliver Zucker, Irving H. Lisco, Steven J. Wang, Han-Jun Timeline of Multi-Organ Plasma Extravasation After Bleomycin-Induced Acute Lung Injury |
title | Timeline of Multi-Organ Plasma Extravasation After Bleomycin-Induced Acute Lung Injury |
title_full | Timeline of Multi-Organ Plasma Extravasation After Bleomycin-Induced Acute Lung Injury |
title_fullStr | Timeline of Multi-Organ Plasma Extravasation After Bleomycin-Induced Acute Lung Injury |
title_full_unstemmed | Timeline of Multi-Organ Plasma Extravasation After Bleomycin-Induced Acute Lung Injury |
title_short | Timeline of Multi-Organ Plasma Extravasation After Bleomycin-Induced Acute Lung Injury |
title_sort | timeline of multi-organ plasma extravasation after bleomycin-induced acute lung injury |
topic | Physiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8841715/ https://www.ncbi.nlm.nih.gov/pubmed/35173628 http://dx.doi.org/10.3389/fphys.2022.777072 |
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