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Quantification of Adventitial Vasa Vasorum Vascularization in Double-injury Restenotic Arteries
BACKGROUND: Accumulating evidence indicates a potential role of adventitial vasa vasorum (VV) dysfunction in the pathophysiology of restenosis. However, characterization of VV vascularization in restenotic arteries with primary lesions is still missing. In this study, we quantitatively evaluated the...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4717968/ https://www.ncbi.nlm.nih.gov/pubmed/26228224 http://dx.doi.org/10.4103/0366-6999.161380 |
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author | Ye, Meng Zhang, Bai-Gen Zhang, Lan Xie, Hui Zhang, Hao |
author_facet | Ye, Meng Zhang, Bai-Gen Zhang, Lan Xie, Hui Zhang, Hao |
author_sort | Ye, Meng |
collection | PubMed |
description | BACKGROUND: Accumulating evidence indicates a potential role of adventitial vasa vasorum (VV) dysfunction in the pathophysiology of restenosis. However, characterization of VV vascularization in restenotic arteries with primary lesions is still missing. In this study, we quantitatively evaluated the response of adventitial VV to vascular injury resulting from balloon angioplasty in diseased arteries. METHODS: Primary atherosclerotic-like lesions were induced by the placement of an absorbable thread surrounding the carotid artery of New Zealand rabbits. Four weeks following double-injury induced that was induced by secondary balloon dilation, three-dimensional patterns of adventitial VV were reconstructed; the number, density, and endothelial surface of VV were quantified using micro-computed tomography. Histology and immunohistochemistry were performed in order to examine the development of intimal hyperplasia. RESULTS: Results from our study suggest that double injured arteries have a greater number of VV, increased luminal surface, and an elevation in the intima/media ratio (I/M), along with an accumulation of macrophages and smooth muscle cells in the intima, as compared to sham or single injury arteries. I/M and the number of VV were positively correlated (R(2) = 0.82, P < 0.001). CONCLUSIONS: Extensive adventitial VV neovascularization occurs in injured arteries after balloon angioplasty, which is associated with intimal hyperplasia. Quantitative assessment of adventitial VV response may provide insight into the basic biological process of postangioplasty restenosis. |
format | Online Article Text |
id | pubmed-4717968 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-47179682016-04-04 Quantification of Adventitial Vasa Vasorum Vascularization in Double-injury Restenotic Arteries Ye, Meng Zhang, Bai-Gen Zhang, Lan Xie, Hui Zhang, Hao Chin Med J (Engl) Original Article BACKGROUND: Accumulating evidence indicates a potential role of adventitial vasa vasorum (VV) dysfunction in the pathophysiology of restenosis. However, characterization of VV vascularization in restenotic arteries with primary lesions is still missing. In this study, we quantitatively evaluated the response of adventitial VV to vascular injury resulting from balloon angioplasty in diseased arteries. METHODS: Primary atherosclerotic-like lesions were induced by the placement of an absorbable thread surrounding the carotid artery of New Zealand rabbits. Four weeks following double-injury induced that was induced by secondary balloon dilation, three-dimensional patterns of adventitial VV were reconstructed; the number, density, and endothelial surface of VV were quantified using micro-computed tomography. Histology and immunohistochemistry were performed in order to examine the development of intimal hyperplasia. RESULTS: Results from our study suggest that double injured arteries have a greater number of VV, increased luminal surface, and an elevation in the intima/media ratio (I/M), along with an accumulation of macrophages and smooth muscle cells in the intima, as compared to sham or single injury arteries. I/M and the number of VV were positively correlated (R(2) = 0.82, P < 0.001). CONCLUSIONS: Extensive adventitial VV neovascularization occurs in injured arteries after balloon angioplasty, which is associated with intimal hyperplasia. Quantitative assessment of adventitial VV response may provide insight into the basic biological process of postangioplasty restenosis. Medknow Publications & Media Pvt Ltd 2015-08-05 /pmc/articles/PMC4717968/ /pubmed/26228224 http://dx.doi.org/10.4103/0366-6999.161380 Text en Copyright: © 2015 Chinese Medical Journal http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms. |
spellingShingle | Original Article Ye, Meng Zhang, Bai-Gen Zhang, Lan Xie, Hui Zhang, Hao Quantification of Adventitial Vasa Vasorum Vascularization in Double-injury Restenotic Arteries |
title | Quantification of Adventitial Vasa Vasorum Vascularization in Double-injury Restenotic Arteries |
title_full | Quantification of Adventitial Vasa Vasorum Vascularization in Double-injury Restenotic Arteries |
title_fullStr | Quantification of Adventitial Vasa Vasorum Vascularization in Double-injury Restenotic Arteries |
title_full_unstemmed | Quantification of Adventitial Vasa Vasorum Vascularization in Double-injury Restenotic Arteries |
title_short | Quantification of Adventitial Vasa Vasorum Vascularization in Double-injury Restenotic Arteries |
title_sort | quantification of adventitial vasa vasorum vascularization in double-injury restenotic arteries |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4717968/ https://www.ncbi.nlm.nih.gov/pubmed/26228224 http://dx.doi.org/10.4103/0366-6999.161380 |
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