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Establishing an economical and widely accessible donation after circulatory death animal abattoir model for lung research using ex vivo lung perfusion
BACKGROUND: Ex vivo lung perfusion (EVLP), is a platform that allows simultaneous testing and treatment of the lungs. However, use of EVLP is costly and requires access to lab animals and accompanying facilities. To increase the use of EVLP for research, we developed a method to perform EVLP using a...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9796928/ https://www.ncbi.nlm.nih.gov/pubmed/35730930 http://dx.doi.org/10.1111/aor.14345 |
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author | Zhang, Zhang Long Moeslund, Niels Hu, Michiel Andy Hoffmann, Roland Venema, Leonie Harmina Van De Wauwer, Caroline Timens, Wim Okamoto, Toshihiro Verschuuren, Erik Alfons Maria Leuvenink, Henri Gerrit Derk Eiskjaer, Hans Erasmus, Michiel Elardus |
author_facet | Zhang, Zhang Long Moeslund, Niels Hu, Michiel Andy Hoffmann, Roland Venema, Leonie Harmina Van De Wauwer, Caroline Timens, Wim Okamoto, Toshihiro Verschuuren, Erik Alfons Maria Leuvenink, Henri Gerrit Derk Eiskjaer, Hans Erasmus, Michiel Elardus |
author_sort | Zhang, Zhang Long |
collection | PubMed |
description | BACKGROUND: Ex vivo lung perfusion (EVLP), is a platform that allows simultaneous testing and treatment of the lungs. However, use of EVLP is costly and requires access to lab animals and accompanying facilities. To increase the use of EVLP for research, we developed a method to perform EVLP using abattoir procured lungs. Furthermore, we were also able to significantly decrease costs. METHODS: Six pair of lungs were procured from abattoir sheep. The lungs were then flushed and stored in ice for 3 h. A low‐flow (20% of cardiac output) approach, a tidal volume of 6 ml/kg bodyweight and total perfusion time of 3 h were chosen. Perfusion fluids and circuits were self‐made. Lung biopsies, perfusate collection, respiratory values, circulatory pressures were recorded and hourly blood gas analyses were performed. RESULTS: Mean pO(2) remained stable from 60 min (49.3 ± 7.1 kPa) to 180 min (51.5 kPa ± 8.0), p = 0.66. Pulmonary artery pressure remained ≤15 mm Hg and the left atrial pressure remained between 3 and 5 mm Hg and peak respiratory pressures ≤20 cmH(2)O. Lactate dehydrogenase increased from start (96.3 ± 56.4 U/L) to the end of perfusion (315.8 ± 85.0 U/L), p < 0.05. No difference was observed in ATP between procurement and post‐EVLP, 129.7 ± 37.4 μmol/g protein to 132.0 ± 23.4 μmol/g, p = 0.92. CONCLUSIONS: Sheep lungs, acquired from an abattoir, can be ex vivo perfused under similar conditions as lab animal lungs with similar results regarding e.g., oxygenation and ATP restoration. Furthermore, costs can be significantly reduced by making use of this abattoir model. By increasing accessibility and lowering costs for experiments using lung perfusion, more results may be achieved in the field of lung diseases. |
format | Online Article Text |
id | pubmed-9796928 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-97969282023-01-04 Establishing an economical and widely accessible donation after circulatory death animal abattoir model for lung research using ex vivo lung perfusion Zhang, Zhang Long Moeslund, Niels Hu, Michiel Andy Hoffmann, Roland Venema, Leonie Harmina Van De Wauwer, Caroline Timens, Wim Okamoto, Toshihiro Verschuuren, Erik Alfons Maria Leuvenink, Henri Gerrit Derk Eiskjaer, Hans Erasmus, Michiel Elardus Artif Organs Main Text BACKGROUND: Ex vivo lung perfusion (EVLP), is a platform that allows simultaneous testing and treatment of the lungs. However, use of EVLP is costly and requires access to lab animals and accompanying facilities. To increase the use of EVLP for research, we developed a method to perform EVLP using abattoir procured lungs. Furthermore, we were also able to significantly decrease costs. METHODS: Six pair of lungs were procured from abattoir sheep. The lungs were then flushed and stored in ice for 3 h. A low‐flow (20% of cardiac output) approach, a tidal volume of 6 ml/kg bodyweight and total perfusion time of 3 h were chosen. Perfusion fluids and circuits were self‐made. Lung biopsies, perfusate collection, respiratory values, circulatory pressures were recorded and hourly blood gas analyses were performed. RESULTS: Mean pO(2) remained stable from 60 min (49.3 ± 7.1 kPa) to 180 min (51.5 kPa ± 8.0), p = 0.66. Pulmonary artery pressure remained ≤15 mm Hg and the left atrial pressure remained between 3 and 5 mm Hg and peak respiratory pressures ≤20 cmH(2)O. Lactate dehydrogenase increased from start (96.3 ± 56.4 U/L) to the end of perfusion (315.8 ± 85.0 U/L), p < 0.05. No difference was observed in ATP between procurement and post‐EVLP, 129.7 ± 37.4 μmol/g protein to 132.0 ± 23.4 μmol/g, p = 0.92. CONCLUSIONS: Sheep lungs, acquired from an abattoir, can be ex vivo perfused under similar conditions as lab animal lungs with similar results regarding e.g., oxygenation and ATP restoration. Furthermore, costs can be significantly reduced by making use of this abattoir model. By increasing accessibility and lowering costs for experiments using lung perfusion, more results may be achieved in the field of lung diseases. John Wiley and Sons Inc. 2022-07-20 2022-11 /pmc/articles/PMC9796928/ /pubmed/35730930 http://dx.doi.org/10.1111/aor.14345 Text en © 2022 The Authors. Artificial Organs published by International Center for Artificial Organ and Transplantation (ICAOT) and Wiley Periodicals LLC. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Main Text Zhang, Zhang Long Moeslund, Niels Hu, Michiel Andy Hoffmann, Roland Venema, Leonie Harmina Van De Wauwer, Caroline Timens, Wim Okamoto, Toshihiro Verschuuren, Erik Alfons Maria Leuvenink, Henri Gerrit Derk Eiskjaer, Hans Erasmus, Michiel Elardus Establishing an economical and widely accessible donation after circulatory death animal abattoir model for lung research using ex vivo lung perfusion |
title | Establishing an economical and widely accessible donation after circulatory death animal abattoir model for lung research using ex vivo lung perfusion |
title_full | Establishing an economical and widely accessible donation after circulatory death animal abattoir model for lung research using ex vivo lung perfusion |
title_fullStr | Establishing an economical and widely accessible donation after circulatory death animal abattoir model for lung research using ex vivo lung perfusion |
title_full_unstemmed | Establishing an economical and widely accessible donation after circulatory death animal abattoir model for lung research using ex vivo lung perfusion |
title_short | Establishing an economical and widely accessible donation after circulatory death animal abattoir model for lung research using ex vivo lung perfusion |
title_sort | establishing an economical and widely accessible donation after circulatory death animal abattoir model for lung research using ex vivo lung perfusion |
topic | Main Text |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9796928/ https://www.ncbi.nlm.nih.gov/pubmed/35730930 http://dx.doi.org/10.1111/aor.14345 |
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