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A 1D model characterizing the role of spatiotemporal contraction distributions on lymph transport
Lymphedema is a condition in which lymph transport is compromised. The factors that govern the timing of lymphatic contractions are largely unknown; however, these factors likely play a central role in lymphatic health. Computational models have proven useful in quantifying changes in lymph transpor...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10692214/ https://www.ncbi.nlm.nih.gov/pubmed/38040740 http://dx.doi.org/10.1038/s41598-023-48131-3 |
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author | Sedaghati, Farbod Dixon, J. Brandon Gleason, Rudolph L. |
author_facet | Sedaghati, Farbod Dixon, J. Brandon Gleason, Rudolph L. |
author_sort | Sedaghati, Farbod |
collection | PubMed |
description | Lymphedema is a condition in which lymph transport is compromised. The factors that govern the timing of lymphatic contractions are largely unknown; however, these factors likely play a central role in lymphatic health. Computational models have proven useful in quantifying changes in lymph transport; nevertheless, there is still much unknown regarding the regulation of contractions. The purpose of this paper is to utilize computational modeling to examine the role of pacemaking activity in lymph transport. A 1D fluid–solid modeling framework was utilized to describe the interaction between the contracting vessel and the lymph flow. The distribution of contractions along a three-lymphangion chain in time and space was determined by specifying the pacemaking sites and parameters obtained from experimentation. The model effectively replicates the contractility patterns in experiments. Quantitatively, the flow rates were measured at 5.44 and 2.29 [Formula: see text] , and the EF values were 78% and less than 33% in the WT and KO models, respectively, which are consistent with the literature. Applying pacemaking parameters in this modeling framework effectively captures lymphatic contractile wave propagations and their relation to lymph transport. It can serve as a motivation for conducting novel studies to evaluate lymphatic pumping function during the development of lymphedema. |
format | Online Article Text |
id | pubmed-10692214 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-106922142023-12-03 A 1D model characterizing the role of spatiotemporal contraction distributions on lymph transport Sedaghati, Farbod Dixon, J. Brandon Gleason, Rudolph L. Sci Rep Article Lymphedema is a condition in which lymph transport is compromised. The factors that govern the timing of lymphatic contractions are largely unknown; however, these factors likely play a central role in lymphatic health. Computational models have proven useful in quantifying changes in lymph transport; nevertheless, there is still much unknown regarding the regulation of contractions. The purpose of this paper is to utilize computational modeling to examine the role of pacemaking activity in lymph transport. A 1D fluid–solid modeling framework was utilized to describe the interaction between the contracting vessel and the lymph flow. The distribution of contractions along a three-lymphangion chain in time and space was determined by specifying the pacemaking sites and parameters obtained from experimentation. The model effectively replicates the contractility patterns in experiments. Quantitatively, the flow rates were measured at 5.44 and 2.29 [Formula: see text] , and the EF values were 78% and less than 33% in the WT and KO models, respectively, which are consistent with the literature. Applying pacemaking parameters in this modeling framework effectively captures lymphatic contractile wave propagations and their relation to lymph transport. It can serve as a motivation for conducting novel studies to evaluate lymphatic pumping function during the development of lymphedema. Nature Publishing Group UK 2023-12-01 /pmc/articles/PMC10692214/ /pubmed/38040740 http://dx.doi.org/10.1038/s41598-023-48131-3 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This 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 | Article Sedaghati, Farbod Dixon, J. Brandon Gleason, Rudolph L. A 1D model characterizing the role of spatiotemporal contraction distributions on lymph transport |
title | A 1D model characterizing the role of spatiotemporal contraction distributions on lymph transport |
title_full | A 1D model characterizing the role of spatiotemporal contraction distributions on lymph transport |
title_fullStr | A 1D model characterizing the role of spatiotemporal contraction distributions on lymph transport |
title_full_unstemmed | A 1D model characterizing the role of spatiotemporal contraction distributions on lymph transport |
title_short | A 1D model characterizing the role of spatiotemporal contraction distributions on lymph transport |
title_sort | 1d model characterizing the role of spatiotemporal contraction distributions on lymph transport |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10692214/ https://www.ncbi.nlm.nih.gov/pubmed/38040740 http://dx.doi.org/10.1038/s41598-023-48131-3 |
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