Biomechanical Characterization of Abdominal Aortic Aneurysm: The Rupture Mechanism

In this work, a four-week-old male C57Bl/6 mouse model of abdominal aortic aneurysm (AAA) was developed to examine the AAA rupture mechanism. Immunofluorescence staining was adopted for quantifying the degradation of elastin, and Picrosirius Red staining was adopted for evaluating the density of col...

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Main Authors: Yingnan Zhai, Ana Isabel Delgado, Mahyar Sameti, Pengfei Dong, Wanfen Xiong, Chris A. Bashur, Linxia Gu
Format: Article
Language:English
Published: MDPI AG 2024-01-01
Series:Applied Sciences
Subjects:
Online Access:https://www.mdpi.com/2076-3417/14/2/613
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author Yingnan Zhai
Ana Isabel Delgado
Mahyar Sameti
Pengfei Dong
Wanfen Xiong
Chris A. Bashur
Linxia Gu
author_facet Yingnan Zhai
Ana Isabel Delgado
Mahyar Sameti
Pengfei Dong
Wanfen Xiong
Chris A. Bashur
Linxia Gu
author_sort Yingnan Zhai
collection DOAJ
description In this work, a four-week-old male C57Bl/6 mouse model of abdominal aortic aneurysm (AAA) was developed to examine the AAA rupture mechanism. Immunofluorescence staining was adopted for quantifying the degradation of elastin, and Picrosirius Red staining was adopted for evaluating the density of collagen. Atomic force microscopy with two probe tip sizes of 5 µm and 20 nm was adopted for mechanical characterization of the AAA. The microstructure changes and stiffness changes in both AAA samples and controlled samples were inspected. The degradation of elastin, wall thickening, formation of micro vessels, and increased density of collagen were observed in the AAA samples. The AAA samples also exhibited fragmented texture from AFM scanning. The histogram of stiffness measurements of the AAA samples with a 20 nm tip demonstrated two unique peak frequencies of stiffness intervals (0–10 kPa and 40–50 kPa). The stiffer regions were correlated with the increased density of collagen, as shown in the immunofluorescence images. The softer regions, combined with the fragmented texture, could be the key index contributing to the initiation and propagation of AAA rupture. Overall, the AAA group showed a higher stiffness than the control group (50.77 ± 62.4 kPa vs. 40.6 ± 51.86 kPa). The findings from this work may help in explaining ruptures in small AAA (<5.5 mm), which account for ten percent of all AAA ruptures. Additionally, the observations in this study may help develop early detection methods and innovative treatments for AAA.
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spelling doaj.art-7bef526e3b614f9f91fbb8a76257cbb82024-01-29T13:43:07ZengMDPI AGApplied Sciences2076-34172024-01-0114261310.3390/app14020613Biomechanical Characterization of Abdominal Aortic Aneurysm: The Rupture MechanismYingnan Zhai0Ana Isabel Delgado1Mahyar Sameti2Pengfei Dong3Wanfen Xiong4Chris A. Bashur5Linxia Gu6Department of Biomedical Engineering and Science, Florida Institute of Technology, Melbourne, FL 32901, USADepartment of Biomedical Engineering and Science, Florida Institute of Technology, Melbourne, FL 32901, USADepartment of Biomedical Engineering and Science, Florida Institute of Technology, Melbourne, FL 32901, USADepartment of Biomedical Engineering and Science, Florida Institute of Technology, Melbourne, FL 32901, USADepartment of Surgery, University of Nebraska Medical Center, Omaha, NE 68198, USADepartment of Biomedical Engineering and Science, Florida Institute of Technology, Melbourne, FL 32901, USADepartment of Biomedical Engineering and Science, Florida Institute of Technology, Melbourne, FL 32901, USAIn this work, a four-week-old male C57Bl/6 mouse model of abdominal aortic aneurysm (AAA) was developed to examine the AAA rupture mechanism. Immunofluorescence staining was adopted for quantifying the degradation of elastin, and Picrosirius Red staining was adopted for evaluating the density of collagen. Atomic force microscopy with two probe tip sizes of 5 µm and 20 nm was adopted for mechanical characterization of the AAA. The microstructure changes and stiffness changes in both AAA samples and controlled samples were inspected. The degradation of elastin, wall thickening, formation of micro vessels, and increased density of collagen were observed in the AAA samples. The AAA samples also exhibited fragmented texture from AFM scanning. The histogram of stiffness measurements of the AAA samples with a 20 nm tip demonstrated two unique peak frequencies of stiffness intervals (0–10 kPa and 40–50 kPa). The stiffer regions were correlated with the increased density of collagen, as shown in the immunofluorescence images. The softer regions, combined with the fragmented texture, could be the key index contributing to the initiation and propagation of AAA rupture. Overall, the AAA group showed a higher stiffness than the control group (50.77 ± 62.4 kPa vs. 40.6 ± 51.86 kPa). The findings from this work may help in explaining ruptures in small AAA (<5.5 mm), which account for ten percent of all AAA ruptures. Additionally, the observations in this study may help develop early detection methods and innovative treatments for AAA.https://www.mdpi.com/2076-3417/14/2/613abdominal aortic aneurysmrupture predictionatomic force microscopymechanical characterizationhistological analysis
spellingShingle Yingnan Zhai
Ana Isabel Delgado
Mahyar Sameti
Pengfei Dong
Wanfen Xiong
Chris A. Bashur
Linxia Gu
Biomechanical Characterization of Abdominal Aortic Aneurysm: The Rupture Mechanism
Applied Sciences
abdominal aortic aneurysm
rupture prediction
atomic force microscopy
mechanical characterization
histological analysis
title Biomechanical Characterization of Abdominal Aortic Aneurysm: The Rupture Mechanism
title_full Biomechanical Characterization of Abdominal Aortic Aneurysm: The Rupture Mechanism
title_fullStr Biomechanical Characterization of Abdominal Aortic Aneurysm: The Rupture Mechanism
title_full_unstemmed Biomechanical Characterization of Abdominal Aortic Aneurysm: The Rupture Mechanism
title_short Biomechanical Characterization of Abdominal Aortic Aneurysm: The Rupture Mechanism
title_sort biomechanical characterization of abdominal aortic aneurysm the rupture mechanism
topic abdominal aortic aneurysm
rupture prediction
atomic force microscopy
mechanical characterization
histological analysis
url https://www.mdpi.com/2076-3417/14/2/613
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