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Anatomical basis for the development of a thoracic duct cannulation model without thoracotomy in Large White pigs
BACKGROUND: To collect lymph draining the lungs provides a useful strategy for tracing pulmonary microvascular fluid and protein biology. A methodology that allows for in vivo sampling of efferent pulmonary lymph in real-time in sheep by cannulating the thoracic duct without entering the thoracic ca...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4429499/ https://www.ncbi.nlm.nih.gov/pubmed/25972220 http://dx.doi.org/10.1186/s12917-015-0430-9 |
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author | Yen, Hung-Hsun Murray, Christina M Davies, Helen MS |
author_facet | Yen, Hung-Hsun Murray, Christina M Davies, Helen MS |
author_sort | Yen, Hung-Hsun |
collection | PubMed |
description | BACKGROUND: To collect lymph draining the lungs provides a useful strategy for tracing pulmonary microvascular fluid and protein biology. A methodology that allows for in vivo sampling of efferent pulmonary lymph in real-time in sheep by cannulating the thoracic duct without entering the thoracic cavity was previously established. To develop a similar thoracic duct cannulation model without thoracotomy in pigs, we investigated the anatomy of the left cervico-thoracic regions of 15 Large White (Yorkshire or Yorkshire-dominated) piglets (aged 4–7 weeks). RESULTS: The thoracic duct, together with the left tracheal trunk, joined the cardiovascular system (the ampulla of the thoracic duct) at a site located craniomedial to the first rib on the left in 80 % (12/15) of the piglets. CONCLUSIONS: As the location of the ampulla of the thoracic duct was consistent in most of the piglets, Large White piglets appear to be suitable for the development of a thoracic duct cannulation model without thoracotomy. The anatomical findings in this study will enable the development of further surgical procedures for cannulating the thoracic duct without thoracotomy, with minimal damage to local tissue, and without transecting any major blood vessels, nerves or muscle bellies. The establishment of a thoracic duct cannulation model for collecting in vivo, in situ efferent lymph, including pulmonary lymph, in pigs without entering the thoracic cavity would be invaluable for many immunological studies, studies on pulmonary immune responses in particular. |
format | Online Article Text |
id | pubmed-4429499 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-44294992015-05-14 Anatomical basis for the development of a thoracic duct cannulation model without thoracotomy in Large White pigs Yen, Hung-Hsun Murray, Christina M Davies, Helen MS BMC Vet Res Methodology Article BACKGROUND: To collect lymph draining the lungs provides a useful strategy for tracing pulmonary microvascular fluid and protein biology. A methodology that allows for in vivo sampling of efferent pulmonary lymph in real-time in sheep by cannulating the thoracic duct without entering the thoracic cavity was previously established. To develop a similar thoracic duct cannulation model without thoracotomy in pigs, we investigated the anatomy of the left cervico-thoracic regions of 15 Large White (Yorkshire or Yorkshire-dominated) piglets (aged 4–7 weeks). RESULTS: The thoracic duct, together with the left tracheal trunk, joined the cardiovascular system (the ampulla of the thoracic duct) at a site located craniomedial to the first rib on the left in 80 % (12/15) of the piglets. CONCLUSIONS: As the location of the ampulla of the thoracic duct was consistent in most of the piglets, Large White piglets appear to be suitable for the development of a thoracic duct cannulation model without thoracotomy. The anatomical findings in this study will enable the development of further surgical procedures for cannulating the thoracic duct without thoracotomy, with minimal damage to local tissue, and without transecting any major blood vessels, nerves or muscle bellies. The establishment of a thoracic duct cannulation model for collecting in vivo, in situ efferent lymph, including pulmonary lymph, in pigs without entering the thoracic cavity would be invaluable for many immunological studies, studies on pulmonary immune responses in particular. BioMed Central 2015-05-14 /pmc/articles/PMC4429499/ /pubmed/25972220 http://dx.doi.org/10.1186/s12917-015-0430-9 Text en © Yen et al.; licensee BioMed Central. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Methodology Article Yen, Hung-Hsun Murray, Christina M Davies, Helen MS Anatomical basis for the development of a thoracic duct cannulation model without thoracotomy in Large White pigs |
title | Anatomical basis for the development of a thoracic duct cannulation model without thoracotomy in Large White pigs |
title_full | Anatomical basis for the development of a thoracic duct cannulation model without thoracotomy in Large White pigs |
title_fullStr | Anatomical basis for the development of a thoracic duct cannulation model without thoracotomy in Large White pigs |
title_full_unstemmed | Anatomical basis for the development of a thoracic duct cannulation model without thoracotomy in Large White pigs |
title_short | Anatomical basis for the development of a thoracic duct cannulation model without thoracotomy in Large White pigs |
title_sort | anatomical basis for the development of a thoracic duct cannulation model without thoracotomy in large white pigs |
topic | Methodology Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4429499/ https://www.ncbi.nlm.nih.gov/pubmed/25972220 http://dx.doi.org/10.1186/s12917-015-0430-9 |
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