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Trimethylamine N-Oxide Promotes Abdominal Aortic Aneurysm Formation by Aggravating Aortic Smooth Muscle Cell Senescence in Mice

Trimethylamine N-oxide (TMAO) has been linked to cardiovascular disease morbidity and mortality. However, the role of TMAO in the development of abdominal aortic aneurysms (AAAs) is not known. This study investigated the association between TMAO and AAA formation. TMAO and saline were added to the d...

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Autores principales: Hu, Jiaxin, Xu, Jiamin, Shen, Song, Zhang, Wengfeng, Chen, Haiting, Sun, Xuan, Qi, Yu, Zhang, Ying, Zhang, Qi, Guo, Meng, Peng, Ningxin, Xu, Biao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9622512/
https://www.ncbi.nlm.nih.gov/pubmed/35143032
http://dx.doi.org/10.1007/s12265-022-10211-6
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author Hu, Jiaxin
Xu, Jiamin
Shen, Song
Zhang, Wengfeng
Chen, Haiting
Sun, Xuan
Qi, Yu
Zhang, Ying
Zhang, Qi
Guo, Meng
Peng, Ningxin
Xu, Biao
author_facet Hu, Jiaxin
Xu, Jiamin
Shen, Song
Zhang, Wengfeng
Chen, Haiting
Sun, Xuan
Qi, Yu
Zhang, Ying
Zhang, Qi
Guo, Meng
Peng, Ningxin
Xu, Biao
author_sort Hu, Jiaxin
collection PubMed
description Trimethylamine N-oxide (TMAO) has been linked to cardiovascular disease morbidity and mortality. However, the role of TMAO in the development of abdominal aortic aneurysms (AAAs) is not known. This study investigated the association between TMAO and AAA formation. TMAO and saline were added to the drinking water of angiotensin II (AngII)- and calcium chloride (CaCl(2))-induced AAA model mice, respectively. After 4 weeks, the effects of TMAO on AAA development were determined by histology and immunohistology of aortic tissue. The in vitro effects of TMAO were also examined in mouse aortic smooth muscle cells (SMCs). The maximal aortic diameter, incidence of AAA, and degree of elastin degradation were significantly increased in TMAO-treated mice. TMAO also increased the accumulation of the senescence markers p21 and p16, as well as of reactive oxygen species (ROS), matrix metalloproteinase-2 (MMP2), and matrix metalloproteinase-9 (MMP9) in vivo and in vitro. TMAO promoted AAA development in mouse AAA models induced by AngII and CaCl(2) by a mechanism involving cellular senescence. GRAPHICAL ABSTRACT: [Image: see text]
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spelling pubmed-96225122022-11-02 Trimethylamine N-Oxide Promotes Abdominal Aortic Aneurysm Formation by Aggravating Aortic Smooth Muscle Cell Senescence in Mice Hu, Jiaxin Xu, Jiamin Shen, Song Zhang, Wengfeng Chen, Haiting Sun, Xuan Qi, Yu Zhang, Ying Zhang, Qi Guo, Meng Peng, Ningxin Xu, Biao J Cardiovasc Transl Res Original Article Trimethylamine N-oxide (TMAO) has been linked to cardiovascular disease morbidity and mortality. However, the role of TMAO in the development of abdominal aortic aneurysms (AAAs) is not known. This study investigated the association between TMAO and AAA formation. TMAO and saline were added to the drinking water of angiotensin II (AngII)- and calcium chloride (CaCl(2))-induced AAA model mice, respectively. After 4 weeks, the effects of TMAO on AAA development were determined by histology and immunohistology of aortic tissue. The in vitro effects of TMAO were also examined in mouse aortic smooth muscle cells (SMCs). The maximal aortic diameter, incidence of AAA, and degree of elastin degradation were significantly increased in TMAO-treated mice. TMAO also increased the accumulation of the senescence markers p21 and p16, as well as of reactive oxygen species (ROS), matrix metalloproteinase-2 (MMP2), and matrix metalloproteinase-9 (MMP9) in vivo and in vitro. TMAO promoted AAA development in mouse AAA models induced by AngII and CaCl(2) by a mechanism involving cellular senescence. GRAPHICAL ABSTRACT: [Image: see text] Springer US 2022-02-10 2022 /pmc/articles/PMC9622512/ /pubmed/35143032 http://dx.doi.org/10.1007/s12265-022-10211-6 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Original Article
Hu, Jiaxin
Xu, Jiamin
Shen, Song
Zhang, Wengfeng
Chen, Haiting
Sun, Xuan
Qi, Yu
Zhang, Ying
Zhang, Qi
Guo, Meng
Peng, Ningxin
Xu, Biao
Trimethylamine N-Oxide Promotes Abdominal Aortic Aneurysm Formation by Aggravating Aortic Smooth Muscle Cell Senescence in Mice
title Trimethylamine N-Oxide Promotes Abdominal Aortic Aneurysm Formation by Aggravating Aortic Smooth Muscle Cell Senescence in Mice
title_full Trimethylamine N-Oxide Promotes Abdominal Aortic Aneurysm Formation by Aggravating Aortic Smooth Muscle Cell Senescence in Mice
title_fullStr Trimethylamine N-Oxide Promotes Abdominal Aortic Aneurysm Formation by Aggravating Aortic Smooth Muscle Cell Senescence in Mice
title_full_unstemmed Trimethylamine N-Oxide Promotes Abdominal Aortic Aneurysm Formation by Aggravating Aortic Smooth Muscle Cell Senescence in Mice
title_short Trimethylamine N-Oxide Promotes Abdominal Aortic Aneurysm Formation by Aggravating Aortic Smooth Muscle Cell Senescence in Mice
title_sort trimethylamine n-oxide promotes abdominal aortic aneurysm formation by aggravating aortic smooth muscle cell senescence in mice
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9622512/
https://www.ncbi.nlm.nih.gov/pubmed/35143032
http://dx.doi.org/10.1007/s12265-022-10211-6
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