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Adipocyte in vascular wall can induce the rupture of abdominal aortic aneurysm
Abdominal aortic aneurysm (AAA) is a vascular disease involving the gradual dilation of the abdominal aorta. It has been reported that development of AAA is associated with inflammation of the vascular wall; however, the mechanism of AAA rupture is not fully understood. In this study, we investigate...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4976321/ https://www.ncbi.nlm.nih.gov/pubmed/27499372 http://dx.doi.org/10.1038/srep31268 |
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author | Kugo, Hirona Zaima, Nobuhiro Tanaka, Hiroki Mouri, Youhei Yanagimoto, Kenichi Hayamizu, Kohsuke Hashimoto, Keisuke Sasaki, Takeshi Sano, Masaki Yata, Tatsuro Urano, Tetsumei Setou, Mitsutoshi Unno, Naoki Moriyama, Tatsuya |
author_facet | Kugo, Hirona Zaima, Nobuhiro Tanaka, Hiroki Mouri, Youhei Yanagimoto, Kenichi Hayamizu, Kohsuke Hashimoto, Keisuke Sasaki, Takeshi Sano, Masaki Yata, Tatsuro Urano, Tetsumei Setou, Mitsutoshi Unno, Naoki Moriyama, Tatsuya |
author_sort | Kugo, Hirona |
collection | PubMed |
description | Abdominal aortic aneurysm (AAA) is a vascular disease involving the gradual dilation of the abdominal aorta. It has been reported that development of AAA is associated with inflammation of the vascular wall; however, the mechanism of AAA rupture is not fully understood. In this study, we investigated the mechanism underlying AAA rupture using a hypoperfusion-induced animal model. We found that the administration of triolein increased the AAA rupture rate in the animal model and that the number of adipocytes was increased in ruptured vascular walls compared to non-ruptured walls. In the ruptured group, macrophage infiltration and the protein levels of matrix metalloproteinases 2 and 9 were increased in the areas around adipocytes, while collagen-positive areas were decreased in the areas with adipocytes compared to those without adipocytes. The administration of fish oil, which suppresses adipocyte hypertrophy, decreased the number and size of adipocytes, as well as decreased the risk of AAA rupture ratio by 0.23 compared to the triolein administered group. In human AAA samples, the amount of triglyceride in the adventitia was correlated with the diameter of the AAA. These results suggest that AAA rupture is related to the abnormal appearance of adipocytes in the vascular wall. |
format | Online Article Text |
id | pubmed-4976321 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-49763212016-08-22 Adipocyte in vascular wall can induce the rupture of abdominal aortic aneurysm Kugo, Hirona Zaima, Nobuhiro Tanaka, Hiroki Mouri, Youhei Yanagimoto, Kenichi Hayamizu, Kohsuke Hashimoto, Keisuke Sasaki, Takeshi Sano, Masaki Yata, Tatsuro Urano, Tetsumei Setou, Mitsutoshi Unno, Naoki Moriyama, Tatsuya Sci Rep Article Abdominal aortic aneurysm (AAA) is a vascular disease involving the gradual dilation of the abdominal aorta. It has been reported that development of AAA is associated with inflammation of the vascular wall; however, the mechanism of AAA rupture is not fully understood. In this study, we investigated the mechanism underlying AAA rupture using a hypoperfusion-induced animal model. We found that the administration of triolein increased the AAA rupture rate in the animal model and that the number of adipocytes was increased in ruptured vascular walls compared to non-ruptured walls. In the ruptured group, macrophage infiltration and the protein levels of matrix metalloproteinases 2 and 9 were increased in the areas around adipocytes, while collagen-positive areas were decreased in the areas with adipocytes compared to those without adipocytes. The administration of fish oil, which suppresses adipocyte hypertrophy, decreased the number and size of adipocytes, as well as decreased the risk of AAA rupture ratio by 0.23 compared to the triolein administered group. In human AAA samples, the amount of triglyceride in the adventitia was correlated with the diameter of the AAA. These results suggest that AAA rupture is related to the abnormal appearance of adipocytes in the vascular wall. Nature Publishing Group 2016-08-08 /pmc/articles/PMC4976321/ /pubmed/27499372 http://dx.doi.org/10.1038/srep31268 Text en Copyright © 2016, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Kugo, Hirona Zaima, Nobuhiro Tanaka, Hiroki Mouri, Youhei Yanagimoto, Kenichi Hayamizu, Kohsuke Hashimoto, Keisuke Sasaki, Takeshi Sano, Masaki Yata, Tatsuro Urano, Tetsumei Setou, Mitsutoshi Unno, Naoki Moriyama, Tatsuya Adipocyte in vascular wall can induce the rupture of abdominal aortic aneurysm |
title | Adipocyte in vascular wall can induce the rupture of abdominal aortic aneurysm |
title_full | Adipocyte in vascular wall can induce the rupture of abdominal aortic aneurysm |
title_fullStr | Adipocyte in vascular wall can induce the rupture of abdominal aortic aneurysm |
title_full_unstemmed | Adipocyte in vascular wall can induce the rupture of abdominal aortic aneurysm |
title_short | Adipocyte in vascular wall can induce the rupture of abdominal aortic aneurysm |
title_sort | adipocyte in vascular wall can induce the rupture of abdominal aortic aneurysm |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4976321/ https://www.ncbi.nlm.nih.gov/pubmed/27499372 http://dx.doi.org/10.1038/srep31268 |
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