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Microstructure-based constitutive model of coronary artery with active smooth muscle contraction
Currently, there is no full three-dimensional (3D) microstructural mechanical model of coronary artery based on measured microstructure including elastin, collagen and smooth muscle cells. Many structural models employ mean values of vessel microstructure, rather than continuous distributions of mic...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5571218/ https://www.ncbi.nlm.nih.gov/pubmed/28839149 http://dx.doi.org/10.1038/s41598-017-08748-7 |
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author | Chen, H. Kassab, G. S. |
author_facet | Chen, H. Kassab, G. S. |
author_sort | Chen, H. |
collection | PubMed |
description | Currently, there is no full three-dimensional (3D) microstructural mechanical model of coronary artery based on measured microstructure including elastin, collagen and smooth muscle cells. Many structural models employ mean values of vessel microstructure, rather than continuous distributions of microstructure, to predict the mechanical properties of blood vessels. Although some models show good agreements on macroscopic vessel responses, they result in a lower elastin stiffness and earlier collagen recruitment. Hence, a full microstructural constitutive model is required for better understanding vascular biomechanics in health and disease. Here, a 3D microstructural model that accounts for all constituent microstructure is proposed to predict macroscopic and microscopic responses of coronary arteries. Coronary artery microstructural parameters were determined based on previous statistical measurements while mechanical testing of arteries (n = 5) were performed in this study to validate the computational predictions. The proposed model not only provides predictions of active and passive stress distributions of vessel wall, but also enables reliable estimations of material parameters of individual fibers and cells and thus predicts microstructural stresses. The validated microstructural model of coronary artery sheds light on vascular biomechanics and can be extend to diseased vessels for better understanding of initiation, progression and clinical treatment of vascular disease. |
format | Online Article Text |
id | pubmed-5571218 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-55712182017-09-01 Microstructure-based constitutive model of coronary artery with active smooth muscle contraction Chen, H. Kassab, G. S. Sci Rep Article Currently, there is no full three-dimensional (3D) microstructural mechanical model of coronary artery based on measured microstructure including elastin, collagen and smooth muscle cells. Many structural models employ mean values of vessel microstructure, rather than continuous distributions of microstructure, to predict the mechanical properties of blood vessels. Although some models show good agreements on macroscopic vessel responses, they result in a lower elastin stiffness and earlier collagen recruitment. Hence, a full microstructural constitutive model is required for better understanding vascular biomechanics in health and disease. Here, a 3D microstructural model that accounts for all constituent microstructure is proposed to predict macroscopic and microscopic responses of coronary arteries. Coronary artery microstructural parameters were determined based on previous statistical measurements while mechanical testing of arteries (n = 5) were performed in this study to validate the computational predictions. The proposed model not only provides predictions of active and passive stress distributions of vessel wall, but also enables reliable estimations of material parameters of individual fibers and cells and thus predicts microstructural stresses. The validated microstructural model of coronary artery sheds light on vascular biomechanics and can be extend to diseased vessels for better understanding of initiation, progression and clinical treatment of vascular disease. Nature Publishing Group UK 2017-08-24 /pmc/articles/PMC5571218/ /pubmed/28839149 http://dx.doi.org/10.1038/s41598-017-08748-7 Text en © The Author(s) 2017 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Chen, H. Kassab, G. S. Microstructure-based constitutive model of coronary artery with active smooth muscle contraction |
title | Microstructure-based constitutive model of coronary artery with active smooth muscle contraction |
title_full | Microstructure-based constitutive model of coronary artery with active smooth muscle contraction |
title_fullStr | Microstructure-based constitutive model of coronary artery with active smooth muscle contraction |
title_full_unstemmed | Microstructure-based constitutive model of coronary artery with active smooth muscle contraction |
title_short | Microstructure-based constitutive model of coronary artery with active smooth muscle contraction |
title_sort | microstructure-based constitutive model of coronary artery with active smooth muscle contraction |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5571218/ https://www.ncbi.nlm.nih.gov/pubmed/28839149 http://dx.doi.org/10.1038/s41598-017-08748-7 |
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