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A multiscale sliding filament model of lymphatic muscle pumping

The lymphatics maintain fluid balance by returning interstitial fluid to veins via contraction/compression of vessel segments with check valves. Disruption of lymphatic pumping can result in a condition called lymphedema with interstitial fluid accumulation. Lymphedema treatments are often ineffecti...

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Autores principales: Morris, Christopher J., Zawieja, David C., Moore, James E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8595193/
https://www.ncbi.nlm.nih.gov/pubmed/34476656
http://dx.doi.org/10.1007/s10237-021-01501-0
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author Morris, Christopher J.
Zawieja, David C.
Moore, James E.
author_facet Morris, Christopher J.
Zawieja, David C.
Moore, James E.
author_sort Morris, Christopher J.
collection PubMed
description The lymphatics maintain fluid balance by returning interstitial fluid to veins via contraction/compression of vessel segments with check valves. Disruption of lymphatic pumping can result in a condition called lymphedema with interstitial fluid accumulation. Lymphedema treatments are often ineffective, which is partially attributable to insufficient understanding of specialized lymphatic muscle lining the vessels. This muscle exhibits cardiac-like phasic contractions and smooth muscle-like tonic contractions to generate and regulate flow. To understand the relationship between this sub-cellular contractile machinery and organ-level pumping, we have developed a multiscale computational model of phasic and tonic contractions in lymphatic muscle and coupled it to a lymphangion pumping model. Our model uses the sliding filament model (Huxley in Prog Biophys Biophys Chem 7:255–318, 1957) and its adaptation for smooth muscle (Mijailovich in Biophys J 79(5):2667–2681, 2000). Multiple structural arrangements of contractile components and viscoelastic elements were trialed but only one provided physiologic results. We then coupled this model with our previous lumped parameter model of the lymphangion to relate results to experiments. We show that the model produces similar pressure, diameter, and flow tracings to experiments on rat mesenteric lymphatics. This model provides the first estimates of lymphatic muscle contraction energetics and the ability to assess the potential effects of sub-cellular level phenomena such as calcium oscillations on lymphangion outflow. The maximum efficiency value predicted (40%) is at the upper end of estimates for other muscle types. Spontaneous calcium oscillations during diastole were found to increase outflow up to approximately 50% in the range of frequencies and amplitudes tested. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s10237-021-01501-0.
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spelling pubmed-85951932021-11-24 A multiscale sliding filament model of lymphatic muscle pumping Morris, Christopher J. Zawieja, David C. Moore, James E. Biomech Model Mechanobiol Original Paper The lymphatics maintain fluid balance by returning interstitial fluid to veins via contraction/compression of vessel segments with check valves. Disruption of lymphatic pumping can result in a condition called lymphedema with interstitial fluid accumulation. Lymphedema treatments are often ineffective, which is partially attributable to insufficient understanding of specialized lymphatic muscle lining the vessels. This muscle exhibits cardiac-like phasic contractions and smooth muscle-like tonic contractions to generate and regulate flow. To understand the relationship between this sub-cellular contractile machinery and organ-level pumping, we have developed a multiscale computational model of phasic and tonic contractions in lymphatic muscle and coupled it to a lymphangion pumping model. Our model uses the sliding filament model (Huxley in Prog Biophys Biophys Chem 7:255–318, 1957) and its adaptation for smooth muscle (Mijailovich in Biophys J 79(5):2667–2681, 2000). Multiple structural arrangements of contractile components and viscoelastic elements were trialed but only one provided physiologic results. We then coupled this model with our previous lumped parameter model of the lymphangion to relate results to experiments. We show that the model produces similar pressure, diameter, and flow tracings to experiments on rat mesenteric lymphatics. This model provides the first estimates of lymphatic muscle contraction energetics and the ability to assess the potential effects of sub-cellular level phenomena such as calcium oscillations on lymphangion outflow. The maximum efficiency value predicted (40%) is at the upper end of estimates for other muscle types. Spontaneous calcium oscillations during diastole were found to increase outflow up to approximately 50% in the range of frequencies and amplitudes tested. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s10237-021-01501-0. Springer Berlin Heidelberg 2021-09-02 2021 /pmc/articles/PMC8595193/ /pubmed/34476656 http://dx.doi.org/10.1007/s10237-021-01501-0 Text en © The Author(s) 2021 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 Original Paper
Morris, Christopher J.
Zawieja, David C.
Moore, James E.
A multiscale sliding filament model of lymphatic muscle pumping
title A multiscale sliding filament model of lymphatic muscle pumping
title_full A multiscale sliding filament model of lymphatic muscle pumping
title_fullStr A multiscale sliding filament model of lymphatic muscle pumping
title_full_unstemmed A multiscale sliding filament model of lymphatic muscle pumping
title_short A multiscale sliding filament model of lymphatic muscle pumping
title_sort multiscale sliding filament model of lymphatic muscle pumping
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8595193/
https://www.ncbi.nlm.nih.gov/pubmed/34476656
http://dx.doi.org/10.1007/s10237-021-01501-0
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