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Negative pressure ventilation enhances acinar perfusion in isolated rat lungs
We compared acinar perfusion in isolated rat lungs ventilated using positive or negative pressures. The lungs were ventilated with air at transpulmomary pressures of 15/5 cm H(2)O, at 25 breaths/min, and perfused with a hetastarch solution at P(pulm art)/P(LA) pressures of 10/0 cm H(2)O. We evaluate...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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SAGE Publications
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5768275/ https://www.ncbi.nlm.nih.gov/pubmed/29283015 http://dx.doi.org/10.1177/2045893217753596 |
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author | Watson, Kal E. Segal, Gilad S. Conhaim, Robert L. |
author_facet | Watson, Kal E. Segal, Gilad S. Conhaim, Robert L. |
author_sort | Watson, Kal E. |
collection | PubMed |
description | We compared acinar perfusion in isolated rat lungs ventilated using positive or negative pressures. The lungs were ventilated with air at transpulmomary pressures of 15/5 cm H(2)O, at 25 breaths/min, and perfused with a hetastarch solution at P(pulm art)/P(LA) pressures of 10/0 cm H(2)O. We evaluated overall perfusability from perfusate flows, and from the venous concentrations of 4-µm diameter fluorescent latex particles infused into the pulmonary circulation during perfusion. We measured perfusion distribution from the trapping patterns of those particles within the lung. We infused approximately 9 million red fluorescent particles into each lung, followed 20 min later by an infusion of an equal number of green particles. In positive pressure lungs, 94.7 ± 2.4% of the infused particles remained trapped within the lungs, compared to 86.8 ± 5.6% in negative pressure lungs (P ≤ 0.05). Perfusate flows averaged 2.5 ± 0.1 mL/min in lungs ventilated with positive pressures, compared to 5.6 ± 01 mL/min in lungs ventilated with negative pressures (P ≤ 0.05). Particle infusions had little effect on perfusate flows. In confocal images of dried sections of each lung, red and green particles were co-localized in clusters in positive pressure lungs, suggesting that acinar vessels that lacked particles were collapsed by these pressures thereby preventing perfusion through them. Particles were more broadly and uniformly distributed in negative pressure lungs, suggesting that perfusion in these lungs was also more uniformly distributed. Our results suggest that the acinar circulation is organized as a web, and further suggest that portions of this web are collapsed by positive pressure ventilation. |
format | Online Article Text |
id | pubmed-5768275 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-57682752018-01-18 Negative pressure ventilation enhances acinar perfusion in isolated rat lungs Watson, Kal E. Segal, Gilad S. Conhaim, Robert L. Pulm Circ Research Article We compared acinar perfusion in isolated rat lungs ventilated using positive or negative pressures. The lungs were ventilated with air at transpulmomary pressures of 15/5 cm H(2)O, at 25 breaths/min, and perfused with a hetastarch solution at P(pulm art)/P(LA) pressures of 10/0 cm H(2)O. We evaluated overall perfusability from perfusate flows, and from the venous concentrations of 4-µm diameter fluorescent latex particles infused into the pulmonary circulation during perfusion. We measured perfusion distribution from the trapping patterns of those particles within the lung. We infused approximately 9 million red fluorescent particles into each lung, followed 20 min later by an infusion of an equal number of green particles. In positive pressure lungs, 94.7 ± 2.4% of the infused particles remained trapped within the lungs, compared to 86.8 ± 5.6% in negative pressure lungs (P ≤ 0.05). Perfusate flows averaged 2.5 ± 0.1 mL/min in lungs ventilated with positive pressures, compared to 5.6 ± 01 mL/min in lungs ventilated with negative pressures (P ≤ 0.05). Particle infusions had little effect on perfusate flows. In confocal images of dried sections of each lung, red and green particles were co-localized in clusters in positive pressure lungs, suggesting that acinar vessels that lacked particles were collapsed by these pressures thereby preventing perfusion through them. Particles were more broadly and uniformly distributed in negative pressure lungs, suggesting that perfusion in these lungs was also more uniformly distributed. Our results suggest that the acinar circulation is organized as a web, and further suggest that portions of this web are collapsed by positive pressure ventilation. SAGE Publications 2017-12-28 /pmc/articles/PMC5768275/ /pubmed/29283015 http://dx.doi.org/10.1177/2045893217753596 Text en © The Author(s) 2018 http://creativecommons.org/licenses/by-nc/4.0/ Creative Commons Non Commercial CC BY-NC: This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (http://www.creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Research Article Watson, Kal E. Segal, Gilad S. Conhaim, Robert L. Negative pressure ventilation enhances acinar perfusion in isolated rat lungs |
title | Negative pressure ventilation enhances acinar perfusion in isolated rat lungs |
title_full | Negative pressure ventilation enhances acinar perfusion in isolated rat lungs |
title_fullStr | Negative pressure ventilation enhances acinar perfusion in isolated rat lungs |
title_full_unstemmed | Negative pressure ventilation enhances acinar perfusion in isolated rat lungs |
title_short | Negative pressure ventilation enhances acinar perfusion in isolated rat lungs |
title_sort | negative pressure ventilation enhances acinar perfusion in isolated rat lungs |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5768275/ https://www.ncbi.nlm.nih.gov/pubmed/29283015 http://dx.doi.org/10.1177/2045893217753596 |
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