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Alterations in biomechanical properties and microstructure of colon wall in early-stage experimental colitis
The aim of the current study was to investigate the effects of early-stage dextran sodium sulfate (DSS)-induced mouse colitis on the biomechanical properties and microstructure of colon walls. In the present study, colitis was induced in 8-week-old mice by the oral administration of DSS, and then 10...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
D.A. Spandidos
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5526050/ https://www.ncbi.nlm.nih.gov/pubmed/28810551 http://dx.doi.org/10.3892/etm.2017.4607 |
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author | Gong, Xiaohui Xu, Xiaojuan Lin, Sisi Cheng, Yu Tong, Jianhua Li, Yongyu |
author_facet | Gong, Xiaohui Xu, Xiaojuan Lin, Sisi Cheng, Yu Tong, Jianhua Li, Yongyu |
author_sort | Gong, Xiaohui |
collection | PubMed |
description | The aim of the current study was to investigate the effects of early-stage dextran sodium sulfate (DSS)-induced mouse colitis on the biomechanical properties and microstructure of colon walls. In the present study, colitis was induced in 8-week-old mice by the oral administration of DSS, and then 10 control and 10 experimental colitis samples were harvested. Uniaxial tensile tests were performed to measure the ultimate tensile strength and ultimate stretches of colon tissues. In addition, histological investigations were performed to characterize changes in the microstructure of the colon wall following treatment. The results revealed that the ultimate tensile stresses were 232±33 and 183±25 kPa for the control and DSS groups, respectively (P=0.001). Ultimate stretches at rupture for the control and DSS groups were 1.43±0.04 and 1.51±0.06, respectively (P=0.006). However, there was no statistically significant difference in tissue stiffness between the two groups. Histological analysis demonstrated high numbers of inflammatory cells infiltrated into the stroma in the DSS group, leading to significant submucosa edema. Hyperplasia was also identified in the DSS-treated submucosa, causing a disorganized microstructure within the colon wall. Furthermore, a large number of collagen fibers in the DSS-treated muscular layer were disrupted, and fiber bundles were thinner when compared with the control group. In conclusion, early-stage experimental colitis alters the mechanical properties and microstructural characteristics of the colon walls, further contributing to tissue remodeling in the pathological process. |
format | Online Article Text |
id | pubmed-5526050 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | D.A. Spandidos |
record_format | MEDLINE/PubMed |
spelling | pubmed-55260502017-08-11 Alterations in biomechanical properties and microstructure of colon wall in early-stage experimental colitis Gong, Xiaohui Xu, Xiaojuan Lin, Sisi Cheng, Yu Tong, Jianhua Li, Yongyu Exp Ther Med Articles The aim of the current study was to investigate the effects of early-stage dextran sodium sulfate (DSS)-induced mouse colitis on the biomechanical properties and microstructure of colon walls. In the present study, colitis was induced in 8-week-old mice by the oral administration of DSS, and then 10 control and 10 experimental colitis samples were harvested. Uniaxial tensile tests were performed to measure the ultimate tensile strength and ultimate stretches of colon tissues. In addition, histological investigations were performed to characterize changes in the microstructure of the colon wall following treatment. The results revealed that the ultimate tensile stresses were 232±33 and 183±25 kPa for the control and DSS groups, respectively (P=0.001). Ultimate stretches at rupture for the control and DSS groups were 1.43±0.04 and 1.51±0.06, respectively (P=0.006). However, there was no statistically significant difference in tissue stiffness between the two groups. Histological analysis demonstrated high numbers of inflammatory cells infiltrated into the stroma in the DSS group, leading to significant submucosa edema. Hyperplasia was also identified in the DSS-treated submucosa, causing a disorganized microstructure within the colon wall. Furthermore, a large number of collagen fibers in the DSS-treated muscular layer were disrupted, and fiber bundles were thinner when compared with the control group. In conclusion, early-stage experimental colitis alters the mechanical properties and microstructural characteristics of the colon walls, further contributing to tissue remodeling in the pathological process. D.A. Spandidos 2017-08 2017-06-14 /pmc/articles/PMC5526050/ /pubmed/28810551 http://dx.doi.org/10.3892/etm.2017.4607 Text en Copyright: © Gong et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made. |
spellingShingle | Articles Gong, Xiaohui Xu, Xiaojuan Lin, Sisi Cheng, Yu Tong, Jianhua Li, Yongyu Alterations in biomechanical properties and microstructure of colon wall in early-stage experimental colitis |
title | Alterations in biomechanical properties and microstructure of colon wall in early-stage experimental colitis |
title_full | Alterations in biomechanical properties and microstructure of colon wall in early-stage experimental colitis |
title_fullStr | Alterations in biomechanical properties and microstructure of colon wall in early-stage experimental colitis |
title_full_unstemmed | Alterations in biomechanical properties and microstructure of colon wall in early-stage experimental colitis |
title_short | Alterations in biomechanical properties and microstructure of colon wall in early-stage experimental colitis |
title_sort | alterations in biomechanical properties and microstructure of colon wall in early-stage experimental colitis |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5526050/ https://www.ncbi.nlm.nih.gov/pubmed/28810551 http://dx.doi.org/10.3892/etm.2017.4607 |
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