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Synchrotron x-ray imaging of pulmonary alveoli in respiration in live intact mice
Despite nearly a half century of studies, it has not been fully understood how pulmonary alveoli, the elementary gas exchange units in mammalian lungs, inflate and deflate during respiration. Understanding alveolar dynamics is crucial for treating patients with pulmonary diseases. In-vivo, real-time...
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/PMC4348649/ https://www.ncbi.nlm.nih.gov/pubmed/25737245 http://dx.doi.org/10.1038/srep08760 |
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author | Chang, Soeun Kwon, Namseop Kim, Jinkyung Kohmura, Yoshiki Ishikawa, Tetsuya Rhee, Chin Kook Je, Jung Ho Tsuda, Akira |
author_facet | Chang, Soeun Kwon, Namseop Kim, Jinkyung Kohmura, Yoshiki Ishikawa, Tetsuya Rhee, Chin Kook Je, Jung Ho Tsuda, Akira |
author_sort | Chang, Soeun |
collection | PubMed |
description | Despite nearly a half century of studies, it has not been fully understood how pulmonary alveoli, the elementary gas exchange units in mammalian lungs, inflate and deflate during respiration. Understanding alveolar dynamics is crucial for treating patients with pulmonary diseases. In-vivo, real-time visualization of the alveoli during respiration has been hampered by active lung movement. Previous studies have been therefore limited to alveoli at lung apices or subpleural alveoli under open thorax conditions. Here we report direct and real-time visualization of alveoli of live intact mice during respiration using tracking X-ray microscopy. Our studies, for the first time, determine the alveolar size of normal mice in respiration without positive end expiratory pressure as 58 ± 14 (mean ± s.d.) μm on average, accurately measured in the lung bases as well as the apices. Individual alveoli of normal lungs clearly show heterogeneous inflation from zero to ~25% (6.7 ± 4.7% (mean ± s.d.)) in size. The degree of inflation is higher in the lung bases (8.7 ± 4.3% (mean ± s.d.)) than in the apices (5.7 ± 3.2% (mean ± s.d.)). The fraction of the total tidal volume allocated for alveolar inflation is 34 ± 3.8% (mean ± s.e.m). This study contributes to the better understanding of alveolar dynamics and helps to develop potential treatment options for pulmonary diseases. |
format | Online Article Text |
id | pubmed-4348649 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-43486492015-03-10 Synchrotron x-ray imaging of pulmonary alveoli in respiration in live intact mice Chang, Soeun Kwon, Namseop Kim, Jinkyung Kohmura, Yoshiki Ishikawa, Tetsuya Rhee, Chin Kook Je, Jung Ho Tsuda, Akira Sci Rep Article Despite nearly a half century of studies, it has not been fully understood how pulmonary alveoli, the elementary gas exchange units in mammalian lungs, inflate and deflate during respiration. Understanding alveolar dynamics is crucial for treating patients with pulmonary diseases. In-vivo, real-time visualization of the alveoli during respiration has been hampered by active lung movement. Previous studies have been therefore limited to alveoli at lung apices or subpleural alveoli under open thorax conditions. Here we report direct and real-time visualization of alveoli of live intact mice during respiration using tracking X-ray microscopy. Our studies, for the first time, determine the alveolar size of normal mice in respiration without positive end expiratory pressure as 58 ± 14 (mean ± s.d.) μm on average, accurately measured in the lung bases as well as the apices. Individual alveoli of normal lungs clearly show heterogeneous inflation from zero to ~25% (6.7 ± 4.7% (mean ± s.d.)) in size. The degree of inflation is higher in the lung bases (8.7 ± 4.3% (mean ± s.d.)) than in the apices (5.7 ± 3.2% (mean ± s.d.)). The fraction of the total tidal volume allocated for alveolar inflation is 34 ± 3.8% (mean ± s.e.m). This study contributes to the better understanding of alveolar dynamics and helps to develop potential treatment options for pulmonary diseases. Nature Publishing Group 2015-03-04 /pmc/articles/PMC4348649/ /pubmed/25737245 http://dx.doi.org/10.1038/srep08760 Text en Copyright © 2015, Macmillan Publishers Limited. All rights reserved 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 in order to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Chang, Soeun Kwon, Namseop Kim, Jinkyung Kohmura, Yoshiki Ishikawa, Tetsuya Rhee, Chin Kook Je, Jung Ho Tsuda, Akira Synchrotron x-ray imaging of pulmonary alveoli in respiration in live intact mice |
title | Synchrotron x-ray imaging of pulmonary alveoli in respiration in live intact mice |
title_full | Synchrotron x-ray imaging of pulmonary alveoli in respiration in live intact mice |
title_fullStr | Synchrotron x-ray imaging of pulmonary alveoli in respiration in live intact mice |
title_full_unstemmed | Synchrotron x-ray imaging of pulmonary alveoli in respiration in live intact mice |
title_short | Synchrotron x-ray imaging of pulmonary alveoli in respiration in live intact mice |
title_sort | synchrotron x-ray imaging of pulmonary alveoli in respiration in live intact mice |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4348649/ https://www.ncbi.nlm.nih.gov/pubmed/25737245 http://dx.doi.org/10.1038/srep08760 |
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