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Progressive alterations in microstructural organization and biomechanical response in the ApoE mouse model of aneurysm

AAA is a complex disease that leads to a localized dilation of the infrarenal aorta that develops over years. Longitudinal information in humans has been difficult to obtain for this disease, therefore mouse models have become increasingly used to study the development of AAAs. The objective of this...

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Autores principales: Haskett, Darren, Azhar, Mohamad, Utzinger, Urs, Vande Geest, Jonathan P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Landes Bioscience 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3749278/
https://www.ncbi.nlm.nih.gov/pubmed/23628871
http://dx.doi.org/10.4161/biom.24648
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author Haskett, Darren
Azhar, Mohamad
Utzinger, Urs
Vande Geest, Jonathan P.
author_facet Haskett, Darren
Azhar, Mohamad
Utzinger, Urs
Vande Geest, Jonathan P.
author_sort Haskett, Darren
collection PubMed
description AAA is a complex disease that leads to a localized dilation of the infrarenal aorta that develops over years. Longitudinal information in humans has been difficult to obtain for this disease, therefore mouse models have become increasingly used to study the development of AAAs. The objective of this study was to determine any changes that occur in the biomechanical response and fiber microstructure in the ApoE(−/−) AngII mouse model of aneurysm during disease progression. Adult ApoE(−/−) AngII infused mice along with wild-type controls were taken at 14 and 28 d. Aortas were excised and tested simultaneously for biaxial mechanical response and ECM organization. Data sets were fit to a Fung-type constitutive model to give peak strains and stiffness values. Images from two photon microscopy were quantified in order to assess the preferred fiber alignment and degree of fiber orientation. Biomechanical results found significant differences that were present at 14 d had returned to normal by 28 d along with significant changes in fiber orientation and dispersion indicating remodeling occurring within the aneurysmal wall. This return of some of the normal biomechanical function, in addition the continuing changes that occur in the microstructure suggest a restorative response that occurs in the ApoE(−/−) AngII infused model after the initial aneurysm formation.
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spelling pubmed-37492782013-08-29 Progressive alterations in microstructural organization and biomechanical response in the ApoE mouse model of aneurysm Haskett, Darren Azhar, Mohamad Utzinger, Urs Vande Geest, Jonathan P. Biomatter Special Focus Report AAA is a complex disease that leads to a localized dilation of the infrarenal aorta that develops over years. Longitudinal information in humans has been difficult to obtain for this disease, therefore mouse models have become increasingly used to study the development of AAAs. The objective of this study was to determine any changes that occur in the biomechanical response and fiber microstructure in the ApoE(−/−) AngII mouse model of aneurysm during disease progression. Adult ApoE(−/−) AngII infused mice along with wild-type controls were taken at 14 and 28 d. Aortas were excised and tested simultaneously for biaxial mechanical response and ECM organization. Data sets were fit to a Fung-type constitutive model to give peak strains and stiffness values. Images from two photon microscopy were quantified in order to assess the preferred fiber alignment and degree of fiber orientation. Biomechanical results found significant differences that were present at 14 d had returned to normal by 28 d along with significant changes in fiber orientation and dispersion indicating remodeling occurring within the aneurysmal wall. This return of some of the normal biomechanical function, in addition the continuing changes that occur in the microstructure suggest a restorative response that occurs in the ApoE(−/−) AngII infused model after the initial aneurysm formation. Landes Bioscience 2013-07-01 2013-04-01 /pmc/articles/PMC3749278/ /pubmed/23628871 http://dx.doi.org/10.4161/biom.24648 Text en Copyright © 2013 Landes Bioscience http://creativecommons.org/licenses/by-nc/3.0/ This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited.
spellingShingle Special Focus Report
Haskett, Darren
Azhar, Mohamad
Utzinger, Urs
Vande Geest, Jonathan P.
Progressive alterations in microstructural organization and biomechanical response in the ApoE mouse model of aneurysm
title Progressive alterations in microstructural organization and biomechanical response in the ApoE mouse model of aneurysm
title_full Progressive alterations in microstructural organization and biomechanical response in the ApoE mouse model of aneurysm
title_fullStr Progressive alterations in microstructural organization and biomechanical response in the ApoE mouse model of aneurysm
title_full_unstemmed Progressive alterations in microstructural organization and biomechanical response in the ApoE mouse model of aneurysm
title_short Progressive alterations in microstructural organization and biomechanical response in the ApoE mouse model of aneurysm
title_sort progressive alterations in microstructural organization and biomechanical response in the apoe mouse model of aneurysm
topic Special Focus Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3749278/
https://www.ncbi.nlm.nih.gov/pubmed/23628871
http://dx.doi.org/10.4161/biom.24648
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