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Feasibility study of direct CT lymphangiography in mice: comparison with interstitial CT/MR lymphangiography
OBJECTIVES: To establish a CT lymphangiography method in mice via direct lymph node puncture. METHODS: We injected healthy mice (n = 8) with 50 µl of water-soluble iodine contrast agent (iomeprol; iodine concentration, 350 mg/mL) subcutaneously into the left-rear foot pad (interstitial injection) an...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10290010/ https://www.ncbi.nlm.nih.gov/pubmed/36719498 http://dx.doi.org/10.1007/s00330-023-09423-4 |
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author | Sugawara, Haruto Furuta, Toshihiro Sumiyoshi, Akira Iiyama, Megumi Kamitani, Masaru Suzuki, Aiko Murakami, Arao Abe, Osamu Aoki, Ichio Akai, Hiroyuki |
author_facet | Sugawara, Haruto Furuta, Toshihiro Sumiyoshi, Akira Iiyama, Megumi Kamitani, Masaru Suzuki, Aiko Murakami, Arao Abe, Osamu Aoki, Ichio Akai, Hiroyuki |
author_sort | Sugawara, Haruto |
collection | PubMed |
description | OBJECTIVES: To establish a CT lymphangiography method in mice via direct lymph node puncture. METHODS: We injected healthy mice (n = 8) with 50 µl of water-soluble iodine contrast agent (iomeprol; iodine concentration, 350 mg/mL) subcutaneously into the left-rear foot pad (interstitial injection) and 20 µl of the same contrast agent directly into the popliteal lymph node (direct puncture) 2 days later. Additionally, we performed interstitial MR lymphangiography on eight mice as a control group. We calculated the contrast ratio for each lymph node and visually assessed the depiction of lymph nodes and lymphatic vessels on a three-point scale. RESULTS: The contrast ratios of 2-min post-injection images of sacral and lumbar–aortic lymph nodes were 20.7 ± 16.6 (average ± standard deviation) and 17.1 ± 12.0 in the direct puncture group, which were significantly higher than those detected in the CT or MR interstitial lymphangiography groups (average, 1.8–3.6; p = 0.008–0.019). The visual assessment scores for sacral lymph nodes, lumbar–aortic lymph nodes, and cisterna chyli were significantly better in the direct puncture group than in the CT interstitial injection group (p = 0.036, 0.009 and 0.001, respectively). The lymphatic vessels between these structures were significantly better scored in direct puncture group than in the CT or MR interstitial lymphangiography groups at 2 min after injection (all p ≤ 0.05). CONCLUSIONS: In CT lymphangiography in mice, the direct lymph node puncture provides a better delineation of the lymphatic pathways than the CT/MR interstitial injection method. KEY POINTS: • The contrast ratios of 2-min post-injection images in the direct CT lymphangiography group were significantly higher than those of CT/MR interstitial lymphangiography groups. • The visibility of lymphatic vessels in subjective analysis in the direct CT lymphangiography group was significantly better in the direct puncture group than in the CT/MR interstitial lymphangiography groups. • CT lymphangiography with direct lymph node puncture can provide excellent lymphatic delineation with contrast being maximum at 2 min after injection. |
format | Online Article Text |
id | pubmed-10290010 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-102900102023-06-25 Feasibility study of direct CT lymphangiography in mice: comparison with interstitial CT/MR lymphangiography Sugawara, Haruto Furuta, Toshihiro Sumiyoshi, Akira Iiyama, Megumi Kamitani, Masaru Suzuki, Aiko Murakami, Arao Abe, Osamu Aoki, Ichio Akai, Hiroyuki Eur Radiol Experimental OBJECTIVES: To establish a CT lymphangiography method in mice via direct lymph node puncture. METHODS: We injected healthy mice (n = 8) with 50 µl of water-soluble iodine contrast agent (iomeprol; iodine concentration, 350 mg/mL) subcutaneously into the left-rear foot pad (interstitial injection) and 20 µl of the same contrast agent directly into the popliteal lymph node (direct puncture) 2 days later. Additionally, we performed interstitial MR lymphangiography on eight mice as a control group. We calculated the contrast ratio for each lymph node and visually assessed the depiction of lymph nodes and lymphatic vessels on a three-point scale. RESULTS: The contrast ratios of 2-min post-injection images of sacral and lumbar–aortic lymph nodes were 20.7 ± 16.6 (average ± standard deviation) and 17.1 ± 12.0 in the direct puncture group, which were significantly higher than those detected in the CT or MR interstitial lymphangiography groups (average, 1.8–3.6; p = 0.008–0.019). The visual assessment scores for sacral lymph nodes, lumbar–aortic lymph nodes, and cisterna chyli were significantly better in the direct puncture group than in the CT interstitial injection group (p = 0.036, 0.009 and 0.001, respectively). The lymphatic vessels between these structures were significantly better scored in direct puncture group than in the CT or MR interstitial lymphangiography groups at 2 min after injection (all p ≤ 0.05). CONCLUSIONS: In CT lymphangiography in mice, the direct lymph node puncture provides a better delineation of the lymphatic pathways than the CT/MR interstitial injection method. KEY POINTS: • The contrast ratios of 2-min post-injection images in the direct CT lymphangiography group were significantly higher than those of CT/MR interstitial lymphangiography groups. • The visibility of lymphatic vessels in subjective analysis in the direct CT lymphangiography group was significantly better in the direct puncture group than in the CT/MR interstitial lymphangiography groups. • CT lymphangiography with direct lymph node puncture can provide excellent lymphatic delineation with contrast being maximum at 2 min after injection. Springer Berlin Heidelberg 2023-01-31 2023 /pmc/articles/PMC10290010/ /pubmed/36719498 http://dx.doi.org/10.1007/s00330-023-09423-4 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Experimental Sugawara, Haruto Furuta, Toshihiro Sumiyoshi, Akira Iiyama, Megumi Kamitani, Masaru Suzuki, Aiko Murakami, Arao Abe, Osamu Aoki, Ichio Akai, Hiroyuki Feasibility study of direct CT lymphangiography in mice: comparison with interstitial CT/MR lymphangiography |
title | Feasibility study of direct CT lymphangiography in mice: comparison with interstitial CT/MR lymphangiography |
title_full | Feasibility study of direct CT lymphangiography in mice: comparison with interstitial CT/MR lymphangiography |
title_fullStr | Feasibility study of direct CT lymphangiography in mice: comparison with interstitial CT/MR lymphangiography |
title_full_unstemmed | Feasibility study of direct CT lymphangiography in mice: comparison with interstitial CT/MR lymphangiography |
title_short | Feasibility study of direct CT lymphangiography in mice: comparison with interstitial CT/MR lymphangiography |
title_sort | feasibility study of direct ct lymphangiography in mice: comparison with interstitial ct/mr lymphangiography |
topic | Experimental |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10290010/ https://www.ncbi.nlm.nih.gov/pubmed/36719498 http://dx.doi.org/10.1007/s00330-023-09423-4 |
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