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The gut microbial metabolite trimethylamine N-oxide and cardiovascular diseases
Morbidity and mortality of cardiovascular diseases (CVDs) are exceedingly high worldwide. Researchers have found that the occurrence and development of CVDs are closely related to intestinal microecology. Imbalances in intestinal microecology caused by changes in the composition of the intestinal mi...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9941174/ https://www.ncbi.nlm.nih.gov/pubmed/36824355 http://dx.doi.org/10.3389/fendo.2023.1085041 |
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author | Zhen, Jing Zhou, Zhou He, Meng Han, Hai-Xiang Lv, En-Hui Wen, Peng-Bo Liu, Xin Wang, Yan-Ting Cai, Xun-Chao Tian, Jia-Qi Zhang, Meng-Ying Xiao, Lei Kang, Xing-Xing |
author_facet | Zhen, Jing Zhou, Zhou He, Meng Han, Hai-Xiang Lv, En-Hui Wen, Peng-Bo Liu, Xin Wang, Yan-Ting Cai, Xun-Chao Tian, Jia-Qi Zhang, Meng-Ying Xiao, Lei Kang, Xing-Xing |
author_sort | Zhen, Jing |
collection | PubMed |
description | Morbidity and mortality of cardiovascular diseases (CVDs) are exceedingly high worldwide. Researchers have found that the occurrence and development of CVDs are closely related to intestinal microecology. Imbalances in intestinal microecology caused by changes in the composition of the intestinal microbiota will eventually alter intestinal metabolites, thus transforming the host physiological state from healthy mode to pathological mode. Trimethylamine N-oxide (TMAO) is produced from the metabolism of dietary choline and L-carnitine by intestinal microbiota, and many studies have shown that this important product inhibits cholesterol metabolism, induces platelet aggregation and thrombosis, and promotes atherosclerosis. TMAO is directly or indirectly involved in the pathogenesis of CVDs and is an important risk factor affecting the occurrence and even prognosis of CVDs. This review presents the biological and chemical characteristics of TMAO, and the process of TMAO produced by gut microbiota. In particular, the review focuses on summarizing how the increase of gut microbial metabolite TMAO affects CVDs including atherosclerosis, heart failure, hypertension, arrhythmia, coronary artery disease, and other CVD-related diseases. Understanding the mechanism of how increases in TMAO promotes CVDs will potentially facilitate the identification and development of targeted therapy for CVDs. |
format | Online Article Text |
id | pubmed-9941174 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-99411742023-02-22 The gut microbial metabolite trimethylamine N-oxide and cardiovascular diseases Zhen, Jing Zhou, Zhou He, Meng Han, Hai-Xiang Lv, En-Hui Wen, Peng-Bo Liu, Xin Wang, Yan-Ting Cai, Xun-Chao Tian, Jia-Qi Zhang, Meng-Ying Xiao, Lei Kang, Xing-Xing Front Endocrinol (Lausanne) Endocrinology Morbidity and mortality of cardiovascular diseases (CVDs) are exceedingly high worldwide. Researchers have found that the occurrence and development of CVDs are closely related to intestinal microecology. Imbalances in intestinal microecology caused by changes in the composition of the intestinal microbiota will eventually alter intestinal metabolites, thus transforming the host physiological state from healthy mode to pathological mode. Trimethylamine N-oxide (TMAO) is produced from the metabolism of dietary choline and L-carnitine by intestinal microbiota, and many studies have shown that this important product inhibits cholesterol metabolism, induces platelet aggregation and thrombosis, and promotes atherosclerosis. TMAO is directly or indirectly involved in the pathogenesis of CVDs and is an important risk factor affecting the occurrence and even prognosis of CVDs. This review presents the biological and chemical characteristics of TMAO, and the process of TMAO produced by gut microbiota. In particular, the review focuses on summarizing how the increase of gut microbial metabolite TMAO affects CVDs including atherosclerosis, heart failure, hypertension, arrhythmia, coronary artery disease, and other CVD-related diseases. Understanding the mechanism of how increases in TMAO promotes CVDs will potentially facilitate the identification and development of targeted therapy for CVDs. Frontiers Media S.A. 2023-02-07 /pmc/articles/PMC9941174/ /pubmed/36824355 http://dx.doi.org/10.3389/fendo.2023.1085041 Text en Copyright © 2023 Zhen, Zhou, He, Han, Lv, Wen, Liu, Wang, Cai, Tian, Zhang, Xiao and Kang https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Endocrinology Zhen, Jing Zhou, Zhou He, Meng Han, Hai-Xiang Lv, En-Hui Wen, Peng-Bo Liu, Xin Wang, Yan-Ting Cai, Xun-Chao Tian, Jia-Qi Zhang, Meng-Ying Xiao, Lei Kang, Xing-Xing The gut microbial metabolite trimethylamine N-oxide and cardiovascular diseases |
title | The gut microbial metabolite trimethylamine N-oxide and cardiovascular diseases |
title_full | The gut microbial metabolite trimethylamine N-oxide and cardiovascular diseases |
title_fullStr | The gut microbial metabolite trimethylamine N-oxide and cardiovascular diseases |
title_full_unstemmed | The gut microbial metabolite trimethylamine N-oxide and cardiovascular diseases |
title_short | The gut microbial metabolite trimethylamine N-oxide and cardiovascular diseases |
title_sort | gut microbial metabolite trimethylamine n-oxide and cardiovascular diseases |
topic | Endocrinology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9941174/ https://www.ncbi.nlm.nih.gov/pubmed/36824355 http://dx.doi.org/10.3389/fendo.2023.1085041 |
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