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Detection of murine post-pneumonectomy lung regeneration by (18)FDG PET imaging
BACKGROUND: An intriguing biologic process in most adult mammals is post-pneumonectomy lung regeneration, that is, the removal of one lung (pneumonectomy) results in the rapid compensatory growth of the remaining lung. The spatial dependence and metabolic activity of the rodent lung during compensat...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3504567/ https://www.ncbi.nlm.nih.gov/pubmed/22999160 http://dx.doi.org/10.1186/2191-219X-2-48 |
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author | Gibney, Barry C Park, Mi-Ae Chamoto, Kenji Ysasi, Alexandra Konerding, Moritz A Tsuda, Akira Mentzer, Steven J |
author_facet | Gibney, Barry C Park, Mi-Ae Chamoto, Kenji Ysasi, Alexandra Konerding, Moritz A Tsuda, Akira Mentzer, Steven J |
author_sort | Gibney, Barry C |
collection | PubMed |
description | BACKGROUND: An intriguing biologic process in most adult mammals is post-pneumonectomy lung regeneration, that is, the removal of one lung (pneumonectomy) results in the rapid compensatory growth of the remaining lung. The spatial dependence and metabolic activity of the rodent lung during compensatory lung regeneration is largely unknown. METHODS: To determine if murine lung regeneration could be detected in vivo, we studied inbred mice 3, 7, 14, and 21 days after left pneumonectomy. The remaining lung was imaged using microCT as well as the glucose tracer 2-deoxy-2-[(18) F]fluoro-d-glucose ((18)FDG) and positron-emission tomography (PET). Because of the compliance of the murine chest wall, reproducible imaging required orotracheal intubation and pressure-controlled ventilation during scanning. RESULTS: After left pneumonectomy, the right lung progressively enlarged over the first 3 weeks. The cardiac lobe demonstrated the greatest percentage increase in size. Dry weights of the individual lobes largely mirrored the increase in lung volume. PET/CT imaging was used to identify enhanced metabolic activity within the individual lobes. In the cardiac lobe, (18)FDG uptake was significantly increased in the day 14 cardiac lobe relative to preoperative values (p < .05). In contrast, the (18)FDG uptake in the other three lobes was not statistically significant at any time point. CONCLUSIONS: We conclude that the cardiac lobe is the dominant contributor to compensatory growth after murine pneumonectomy. Further, PET/CT scanning can detect both the volumetric increase and the metabolic changes associated with the regenerative growth in the murine cardiac lobe. |
format | Online Article Text |
id | pubmed-3504567 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Springer |
record_format | MEDLINE/PubMed |
spelling | pubmed-35045672012-11-26 Detection of murine post-pneumonectomy lung regeneration by (18)FDG PET imaging Gibney, Barry C Park, Mi-Ae Chamoto, Kenji Ysasi, Alexandra Konerding, Moritz A Tsuda, Akira Mentzer, Steven J EJNMMI Res Original Research BACKGROUND: An intriguing biologic process in most adult mammals is post-pneumonectomy lung regeneration, that is, the removal of one lung (pneumonectomy) results in the rapid compensatory growth of the remaining lung. The spatial dependence and metabolic activity of the rodent lung during compensatory lung regeneration is largely unknown. METHODS: To determine if murine lung regeneration could be detected in vivo, we studied inbred mice 3, 7, 14, and 21 days after left pneumonectomy. The remaining lung was imaged using microCT as well as the glucose tracer 2-deoxy-2-[(18) F]fluoro-d-glucose ((18)FDG) and positron-emission tomography (PET). Because of the compliance of the murine chest wall, reproducible imaging required orotracheal intubation and pressure-controlled ventilation during scanning. RESULTS: After left pneumonectomy, the right lung progressively enlarged over the first 3 weeks. The cardiac lobe demonstrated the greatest percentage increase in size. Dry weights of the individual lobes largely mirrored the increase in lung volume. PET/CT imaging was used to identify enhanced metabolic activity within the individual lobes. In the cardiac lobe, (18)FDG uptake was significantly increased in the day 14 cardiac lobe relative to preoperative values (p < .05). In contrast, the (18)FDG uptake in the other three lobes was not statistically significant at any time point. CONCLUSIONS: We conclude that the cardiac lobe is the dominant contributor to compensatory growth after murine pneumonectomy. Further, PET/CT scanning can detect both the volumetric increase and the metabolic changes associated with the regenerative growth in the murine cardiac lobe. Springer 2012-09-21 /pmc/articles/PMC3504567/ /pubmed/22999160 http://dx.doi.org/10.1186/2191-219X-2-48 Text en Copyright ©2012 Gibney et al.; licensee Springer. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Research Gibney, Barry C Park, Mi-Ae Chamoto, Kenji Ysasi, Alexandra Konerding, Moritz A Tsuda, Akira Mentzer, Steven J Detection of murine post-pneumonectomy lung regeneration by (18)FDG PET imaging |
title | Detection of murine post-pneumonectomy lung regeneration by (18)FDG PET imaging |
title_full | Detection of murine post-pneumonectomy lung regeneration by (18)FDG PET imaging |
title_fullStr | Detection of murine post-pneumonectomy lung regeneration by (18)FDG PET imaging |
title_full_unstemmed | Detection of murine post-pneumonectomy lung regeneration by (18)FDG PET imaging |
title_short | Detection of murine post-pneumonectomy lung regeneration by (18)FDG PET imaging |
title_sort | detection of murine post-pneumonectomy lung regeneration by (18)fdg pet imaging |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3504567/ https://www.ncbi.nlm.nih.gov/pubmed/22999160 http://dx.doi.org/10.1186/2191-219X-2-48 |
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